1
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Thapa S, Sapkota R, Khati S, Adhikari A. Primary Tracheal Schwannoma With Extension to the Thyroid Gland: Management. Clin Case Rep 2025; 13:e70120. [PMID: 39807220 PMCID: PMC11725490 DOI: 10.1002/ccr3.70120] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/09/2024] [Revised: 11/24/2024] [Accepted: 12/16/2024] [Indexed: 01/16/2025] Open
Abstract
The occurrence of neurogenic tumors in the tracheobronchial tree is uncommon. We report a case of transmural tracheal schwannoma with extraluminal component extending upto the left thyroid lobe. 40-year-old male presented with scanty hemoptysis due to transmural tracheal schwannoma with extraluminal part of tumor extending till the left lobe of thyroid gland. Patient underwent tracheal resection and anastomosis with en-bloc excision of left thyroid lobe due to the nature and size of the tumor. Tracheal Schwannoma are not that frequent. Symptoms can misguide the clinician causing delay in diagnosis from the onset of symptoms. Definitive diagnosis is made after histopathological examination and immunohistochemical studies. So far, resection and anastomosis of trachea has been adequate treatment. Tracheal neoplasms are unusual and tracheal schwannomas are very unique. The case highlights the varied presentation of tracheal schwannoma and confusion faced to diagnose the patient and provide an optimal management.
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Affiliation(s)
- Srijana Thapa
- Manmohan Cardiothoracic Vascular and Transplant Center(MCVTC)Department of CTVS, Thoracic Surgery UnitKathmanduNepal
| | - Ranjan Sapkota
- Manmohan Cardiothoracic Vascular and Transplant Center(MCVTC)Department of CTVS, Thoracic Surgery UnitKathmanduNepal
| | - Srijana Khati
- Tribhuvan University Teaching Hospital(TUTH)KathmanduNepal
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2
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Chan MC, Leung CCD, Chan YH, Ho MY, Chen CH, Ngai CM, Chan HCC, Yeung YC. A Rare Case of Tracheal Schwannoma Successfully Treated With Endoscopic Resection and Cryoablation Under Rigid Bronchoscopy. Case Rep Pulmonol 2024; 2024:2961560. [PMID: 39444951 PMCID: PMC11498987 DOI: 10.1155/2024/2961560] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/23/2024] [Accepted: 10/03/2024] [Indexed: 10/25/2024] Open
Abstract
We present a rare case of tracheal schwannoma, the first reported in Hong Kong, emphasizing the diagnostic challenges and treatment outcomes. A 54-year-old woman with respiratory symptoms underwent evaluations revealing a tracheal mass causing luminal narrowing. Emergency operation with rigid bronchoscopy and cryoablation successfully removed the tumor. Follow-up bronchoscopies showed a gradual reduction in residual tumor size, with no evidence of recurrence after 3.5 years postoperation. Tracheal schwannomas are exceedingly rare, often resulting in delayed diagnosis. Clinicians should maintain a high suspicion of tracheal tumors in patients with unexplained respiratory symptoms. Spirometry and flow volume loop analysis aid in identifying upper airway obstruction. Rigid bronchoscopy is preferred for diagnosis and treatment, ensuring airway stability and obtaining tissue samples. Surgical resection remains the mainstay, but observation after endoscopic resection may be considered. This case highlights the successful management of tracheal schwannoma through endoscopic resection and cryoablation, emphasizing the need for further studies and case reports on this rare entity.
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Affiliation(s)
- Ming Chiu Chan
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
| | | | - Yu Hong Chan
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
| | - Man Ying Ho
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
| | - Chun Hoi Chen
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
| | - Ching Man Ngai
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
| | | | - Yiu Cheong Yeung
- Department of Medicine and Geriatrics, Princess Margaret Hospital, Hong Kong, China
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3
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Afsin E, Yaksi O, Önal A, Bacaksiz E. Tracheal schwannoma mimicking asthma. Int J Neurosci 2024; 134:436-440. [PMID: 35924590 DOI: 10.1080/00207454.2022.2110494] [Citation(s) in RCA: 1] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/22/2021] [Accepted: 07/29/2022] [Indexed: 01/06/2023]
Abstract
Schwannoma in primary neurogenic tumors of the trachea is an extremely rare disease. A 21-year-old male patient with stridor was followed up with a diagnosis of asthma for two years. While no lesion was observed in the chest X-ray, tracheal schwannoma was diagnosed in the case who underwent tracheotomy due to the lesion obstructing the trachea almost completely on chest CT. The clinical findings of the patient improved ultimately in the postoperative period. We aimed to discuss the approach and follow-up of the disease with our case, although it is rare that schwannoma might be in the differential diagnosis of masses with upper airway obstruction.
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Affiliation(s)
- Emine Afsin
- Chest Diseases, Bolu Abant Izzet Baysal Universitesi Tip Fakultesi, Bolu, Turkey
| | - Osman Yaksi
- Toracic Surgery, Bolu Abant Izzet Baysal Universitesi Tip Fakultesi, Bolu, Turkey
| | - Alican Önal
- Pathology, Bolu Abant Izzet Baysal Universitesi Tip Fakultesi, Bolu, Turkey
| | - Emre Bacaksiz
- Chest Diseases, Bolu Abant Izzet Baysal Universitesi Tip Fakultesi, Bolu, Turkey
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4
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Mohamad R, Koubaissi SA, Bou Khalil P, Sfeir P. Tracheal Schwannoma Presenting as Subcutaneous Emphysema and Pneumomediastinum. BMJ Case Rep 2024; 17:e256951. [PMID: 38594197 PMCID: PMC11015168 DOI: 10.1136/bcr-2023-256951] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 01/15/2024] [Indexed: 04/11/2024] Open
Abstract
Primary tracheal schwannomas are rare benign tumours. This is a case report, and therefore, no specific methods or results are applicable. We here report a case of a tracheal schwannoma in an early adolescent girl presenting with subcutaneous emphysema and symptoms of airway obstruction. Tracheal resection and reconstruction by primary anastomosis were performed. Pathology confirmed the diagnosis of tracheal schwannoma. This is an unusual life-threatening presentation of a benign rare tracheal tumour with a challenging approach to management.
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Affiliation(s)
- Rayan Mohamad
- Department of Internal Medicine, American University of Beirut, Beirut, Lebanon
| | - Salwa A Koubaissi
- Department of Internal Medicine, American University of Beirut Medical Center, Beirut, Lebanon
| | - Pierre Bou Khalil
- Department of Internal Medicine, American University of Beirut, Beirut, Lebanon
| | - Pierre Sfeir
- Department of Surgery, American University of Beirut, Beirut, Lebanon
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5
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Lorandi LL, Ceccon FP, Callegari FM, Bacchi CE, Haddad L. Benign cervical schwannoma with tracheal invasion. EINSTEIN-SAO PAULO 2024; 22:eRC0528. [PMID: 38324847 PMCID: PMC10948098 DOI: 10.31744/einstein_journal/2024rc0528] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/15/2023] [Accepted: 11/21/2023] [Indexed: 02/09/2024] Open
Abstract
Schwannomas commonly develop in the cervical region, 25% - 45% of cases are diagnosed in this anatomical region. Tracheal neurogenic tumors are exceedingly rare and can be misdiagnosed as invasive thyroid carcinomas or other infiltrating malignancies when present at the level of the thyroid gland. Here, we present a case of synchronous benign cervical schwannoma with tracheal invasion and papillary thyroid carcinoma in a patient who was initially hospitalized for COVID-19. The patient presented with dyspnea that was later found to be caused by tracheal extension of a cervical tumor. Surgical excision was performed, and the surgical team proceeded with segmental tracheal resection, removal of the cervical mass, and total thyroidectomy. The specimen was sent for pathological analysis, which revealed synchronous findings of a benign cervical schwannoma with tracheal invasion and papillary thyroid carcinoma. The literature on this subject, together with the present case report, suggests that neurogenic tumors should be included in the differential diagnosis of obstructing tracheal cervical masses. Surgical excision is the first-line of treatment for benign cervical schwannomas.
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Affiliation(s)
- Leonardo Lima Lorandi
- Faculdade Israelita de Ciências da Saúde Albert EinsteinHospital Israelita Albert EinsteinSão PauloSPBrazil Faculdade Israelita de Ciências da Saúde Albert Einstein , Hospital Israelita Albert Einstein , São Paulo , SP , Brazil .
| | - Fabio Pupo Ceccon
- Hospital Israelita Albert EinsteinSão PauloSPBrazil Hospital Israelita Albert Einstein , São Paulo , SP , Brazil .
| | - Fabiano Mesquita Callegari
- Pathology DepartmentUniversidade Federal de São PauloSão PauloSPBrazil Pathology Department , Universidade Federal de São Paulo , São Paulo , SP , Brazil .
| | - Carlos Eduardo Bacchi
- Laboratorio de Patologia Bacchi LtdaBotucatuSPBrazil Laboratorio de Patologia Bacchi Ltda , Botucatu , SP , Brazil .
| | - Leonardo Haddad
- Department of Otorhinolaryngology and Head and Neck SurgeryEscola Paulista de MedicinaUniversidade Federal de São PauloSão PauloSPBrazil Department of Otorhinolaryngology and Head and Neck Surgery , Escola Paulista de Medicina , Universidade Federal de São Paulo , São Paulo , SP , Brazil .
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6
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Rafieian S, Ershadi R, Amini H, Samimiat A, Gholinataj Jelodar M, Vahedi M. Primary benign intratracheal schwannoma: A case report and review of the literature. Respirol Case Rep 2023; 11:e01241. [PMID: 37915369 PMCID: PMC10616687 DOI: 10.1002/rcr2.1241] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/12/2023] [Accepted: 10/19/2023] [Indexed: 11/03/2023] Open
Abstract
Shwannomas are rare benign tumours especially in tracheal. A 16-year-old male presented with a chronic cough, and a thoracic CT scan revealed a pedunculated tumour measuring approximately 11 × 13 mm in size, located 22 mm away from the main carina. Tissue sample was obtained via rigid bronchoscopy and cryobiopsy, and the pathological analysis confirmed the diagnosis of a benign nerve sheath tumour consistent with schwannoma. The patient subsequently underwent resection of the tumour and tracheal anastomosis. Schwannomas are uncommon pulmonary tumours that typically occur in adults, with a higher incidence among females. The presenting symptoms vary depending on the size and location of the tumour. Treatment options include therapeutic bronchoscopy or surgical resection, with the choice of approach based on tumour characteristics (pedunculated or sessile), preoperative surgical risk, and risk of recurrence. The prognosis is generally favourable, with a low risk of recurrence and excellent outcomes.
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Affiliation(s)
- Shahab Rafieian
- Department of Thoracic Surgery, Imam Khomeini Hospital ComplexTehran University of Medical SciencesTehranIran
| | - Reza Ershadi
- Department of Thoracic Surgery, Imam Khomeini Hospital ComplexTehran University of Medical SciencesTehranIran
| | - Hesam Amini
- Department of Thoracic Surgery, Imam Khomeini Hospital ComplexTehran University of Medical SciencesTehranIran
| | - Alireza Samimiat
- Department of Surgery, Sina HospitalTehran University of Medical SciencesTehranIran
| | | | - Matin Vahedi
- Department of Surgery, Sina HospitalTehran University of Medical SciencesTehranIran
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7
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Nguyen-Hai C, Vo-Nguyen-Thuan T, Tran-Quyet T, Duong-Quy S. Giant Tracheal Fibroepithelial Polyp Treated Successfully by High-Frequency Electrocautery Ablation. Pulm Ther 2023; 9:281-286. [PMID: 37133681 DOI: 10.1007/s41030-023-00223-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/02/2023] [Accepted: 04/04/2023] [Indexed: 05/04/2023] Open
Abstract
Endotracheal fibroepithelial polyp is a rare disease in the airways. This report describes a rare case of a tracheal giant fibroepithelial polyp. A 17-year-old woman was admitted to the hospital with severe acute respiratory failure. Chest computed tomography revealed a tumor located below the epiglottis. Endotracheal bronchoscopic examination showed a giant polyp. This endotracheal polyp was removed with ablation, by using high-frequency electricity through flexible bronchoscopy under intravenous anesthesia. The patient has had a good recovery after the intervention and at long-term follow-up. We herein describe and discuss the appropriate therapeutic approach and also review the pertinent literature.
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Affiliation(s)
- Cong Nguyen-Hai
- Respiratory Department, Military Hospital 175, Ho Chi Minh City, Vietnam
| | | | - Thang Tran-Quyet
- Department of Diagnostic Imaging, Military Hospital 175, Ho Chi Minh City, Vietnam
| | - Sy Duong-Quy
- Clinical Research Unit, Lam Dong Medical College and Bio-Medical Research Centre, Dalat City, Vietnam.
- Immuno-Allergology and Pulmonology Division, Hershey Medical Center, Medical College, PA, USA.
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8
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Burton KA, Karulf M, Pahn B. Bronchial Schwannoma Incidentally Discovered via Bronchoscopy: A Case Report. Cureus 2023; 15:e38011. [PMID: 37223163 PMCID: PMC10204352 DOI: 10.7759/cureus.38011] [Citation(s) in RCA: 2] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Accepted: 04/22/2023] [Indexed: 05/25/2023] Open
Abstract
Bronchial schwannomas are rare tumors that arise from Schwann cells and account for a very small percentage of primary lung tumors. This case report describes a rare incidental finding of a bronchial schwannoma discovered in the left lower lobe secondary carina via bronchoscopy in a 71-year-old female who presented with minimal symptoms.
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Affiliation(s)
- Kyle A Burton
- Internal Medicine, Michigan State University College of Human Medicine, Marquette, USA
| | - Matthew Karulf
- Pulmonology, Upper Peninsula Health System, Marquette, USA
| | - Brian Pahn
- Pathology, Upper Peninsula Health System, Marquette, USA
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9
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Kim C, Nam H, Ko Y. Two cases of large tracheobronchial schwannomas completely resected by rigid bronchoscopy with multiple instruments. Respirol Case Rep 2023; 11:e01091. [PMID: 36776996 PMCID: PMC9902863 DOI: 10.1002/rcr2.1091] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Grants] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/21/2022] [Accepted: 01/15/2023] [Indexed: 02/10/2023] Open
Abstract
Primary tracheobronchial schwannomas are extremely rare. Surgical treatment has been the first choice for these benign tumours due to the substantial residual rates and recurrences after bronchoscopic resection. In addition, there has been limited information on bronchoscopic removal of endobronchial schwannomas. We describe two cases of large tracheal and bronchial schwannomas that were completely and successfully resected by snare electrocautery, insulation-tipped knife, and argon plasma coagulation under rigid bronchoscopy. These cases highlight that rigid bronchoscopic treatment with these multiple instruments can be a good treatment option for endotracheal or endobronchial schwannomas.
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Affiliation(s)
- Changhwan Kim
- Department of Internal MedicineJeju National University Hospital, Jeju National University School of MedicineJejuSouth Korea
| | - Hae‐Seong Nam
- Division of Pulmonology, Department of Internal MedicineInha University Hospital, Inha University School of MedicineIncheonSouth Korea
| | - Yousang Ko
- Division of Pulmonary, Allergy and Critical Care Medicine, Department of Internal MedicineHallym University Kangdong Sacred Heart HospitalSeoulSouth Korea
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10
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Lina G, Pengguo H, Zhihua X, Jianxin W, Baoqin B, Mingyue Z, Junping S. Tracheobronchial schwannoma: a case report and literature review. J Int Med Res 2023; 51:3000605221149891. [PMID: 36708207 PMCID: PMC9893080 DOI: 10.1177/03000605221149891] [Citation(s) in RCA: 5] [Impact Index Per Article: 2.5] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/29/2023] Open
Abstract
Primary tracheobronchial schwannoma is extremely rare. A woman in her early 60 s was admitted to our department with a 2-month history of cough and expectoration. Chest computed tomography (CT) revealed a high-density nodule at the opening of the right main bronchus, accompanied by atelectasis in the middle and lower lobes. Flexible bronchoscopy revealed a tumor at the opening of the bronchus of the right middle lung lobe, which protruded into the main bronchus. A high-frequency electrosurgical snare, endobronchial cryosurgery, and argon plasma coagulation (APC) were used under rigid bronchoscopy. Histopathological examination diagnosed the tumor as schwannoma. The patient's symptoms resolved after the operation. Follow-up chest CT showed that the right main bronchus was unobstructed, and the bronchus of the lower lobe was open. Bronchoscopic interventional therapy is an alternative treatment for tracheobronchial schwannoma.
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Affiliation(s)
- Guo Lina
- Department of Respiratory and Critical Care Medicine, Datong Third People's Hospital, Datong, Shanxi, China
| | - Hou Pengguo
- Department of Respiratory and Critical Care Medicine, Datong Third People's Hospital, Datong, Shanxi, China
| | - Xiao Zhihua
- Department of Respiratory and Critical Care Medicine, Datong Third People's Hospital, Datong, Shanxi, China
| | - Wang Jianxin
- Department of Respiratory and Critical Care Medicine, The Chinese PLA General Hospital, Fuxing Road, Haidian District, Beijing, China
| | - Bai Baoqin
- Department of Respiratory and Critical Care Medicine, Datong Third People's Hospital, Datong, Shanxi, China
| | - Zhang Mingyue
- Department of Respiratory and Critical Care Medicine, The Chinese PLA General Hospital, Fuxing Road, Haidian District, Beijing, China
| | - Sun Junping
- Department of Respiratory and Critical Care Medicine, The Chinese PLA General Hospital, Fuxing Road, Haidian District, Beijing, China,Sun Junping, Department of Respiratory and Critical Care Medicine, The Chinese PLA General Hospital, Fuxing Road, Haidian District, Beijing 100853, China.
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11
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Othmane B, Mohamed E, Soufiyane K, Youssef R, abdelaziz R. Rare Schwannomas of Head and Neck and Review of Literature. Indian J Otolaryngol Head Neck Surg 2022; 74:6200-6205. [PMID: 36742770 PMCID: PMC9895259 DOI: 10.1007/s12070-021-02878-1] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 07/29/2021] [Accepted: 09/18/2021] [Indexed: 02/07/2023] Open
Abstract
Benign schwannoma is a slow growing encapsulated tumor arising from the sheath of Schwann, The majority had extra-cranial localization. We report in this review three cases of a rare extra cranial localization of benign schwannoma in the trachea, frontal sinus and intraparotid facial nerve. The first case diagnosed in a 10-years-old boy, presented with a painless, slow growing mass evolving for three years in the left parotidic region, total conservative parotidectomy was done. The second case concerned a 38-years-old, was admitted to the emergency department with acute inspiratory dyspnea, endoscopic exploration revealed a polylobed tracheal tumor, complete tumor excision was done endoscopically. The third case was about a 33 years old patient, presented a gradually enlarging frontal swelling associated with headache and left nasal obstruction, the endoscopic examination revealed a gray pinkish, smooth and firm soft tissue mass occupying the entire left nasal cavity, CT scan and MRI were requested to assess the characteristics and extent of the tumor, The surgical intervention combined two approaches: trans facial through a mid-frontal incision, and endonasal one. Histopathological examination confirmed the diagnosis of benign schwannoma in all these cases.
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Affiliation(s)
| | - Elbouderkaoui Mohamed
- Faculty of Medicine of Marrakech, Mohamed VI University Hospital, Marrakech, Morocco
| | - Kajai Soufiyane
- Faculty of Medicine of Marrakech, Mohamed VI University Hospital, Marrakech, Morocco
| | - Rochdi Youssef
- Faculty of Medicine of Marrakech, Mohamed VI University Hospital, Marrakech, Morocco
| | - Raji abdelaziz
- Faculty of Medicine of Marrakech, Mohamed VI University Hospital, Marrakech, Morocco
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12
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Shen YS, Tian XD, Pan Y, Li H. Treatment of primary tracheal schwannoma with endoscopic resection: A case report. World J Clin Cases 2022; 10:10279-10285. [PMID: 36246804 PMCID: PMC9561569 DOI: 10.12998/wjcc.v10.i28.10279] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 05/15/2022] [Revised: 06/21/2022] [Accepted: 08/25/2022] [Indexed: 02/05/2023] Open
Abstract
BACKGROUND Schwannoma is a benign tumor originating from the peripheral nerve sheath. The clinical symptoms of tracheal schwannoma depend on the location of the tumor, and the most common clinical symptoms are cough and hemoptysis. The most effective treatment for benign tumors is complete resection of the primary lesion at an early stage. Our experience has demonstrated that primary tracheal schwannoma can be safely excised with a high-frequency electric knife in a minimally invasive manner.
CASE SUMMARY We report a 61-year-old asymptomatic woman who underwent chest computed tomography (CT), which accidentally found an intraluminal tracheal mass without enlarged lymph nodes. Then, the patient underwent bronchoscopy, which found that the tracheal mass originated from the left wall of the upper trachea, was less than 1.5 cm in size, immovable, smooth and 4 cm away from the vocal cord, resulting in partial upper respiratory tract obstruction. Treatment was performed using an endoscopic resection for en bloc removal of the tracheal mass. The diagnosis was primary tracheal schwannoma. A follow-up was performed after endoscopic surgery, and bronchoscopy and thoracic CT were used to monitor whether there was a recurrence. At present, there is no evidence of recurrence, and the patient had a good quality of life. Endoscopic resection may be effective and safe in the treatment of primary tracheal schwannoma.
CONCLUSION Primary tracheal schwannoma is a very rare benign tumor. In this case, we cured it by complete endoscopic resection.
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Affiliation(s)
- Yong-Shuai Shen
- Department of Endoscopy, Tianjin Cancer Hospital Airport Hospital, Tianjin 300000, China
| | - Xiang-Dong Tian
- Department of Endoscopy, Tianjin Medical University Cancer Institute and Hospital, Tianjin 300060, China
| | - Yi Pan
- Department of Pathology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, China
| | - Hua Li
- Department of Endoscopy, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin’s Clinical Research Center for Cancer, Tianjin 300060, China
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13
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Naomi A, Hujiwara H, Koizumi T, Sakurai Y, Kohashi Y, Yoneda Y, Kitamura Y, Hattori Y, Saitou Y. A case of cervical schwannoma with upper tracheal stenosis followed up as asthma for 4 years. Respirol Case Rep 2022; 10:e01005. [PMID: 35832323 PMCID: PMC9263536 DOI: 10.1002/rcr2.1005] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/25/2022] [Accepted: 06/21/2022] [Indexed: 11/11/2022] Open
Abstract
Cases of upper tracheal stenosis due to cervical schwannoma are fairly rare; therefore, no treatment has been determined. In this case, our patient had been treated for asthma for 4 years and was admitted to our hospital because of exacerbation. Computed tomography showed a tracheal stenosis lesion just below the vocal cords, and a biopsy revealed schwannoma. Conservative therapy was preferred rather than tumour resection by surgery. Follow-up for 5 years showed no changes on imaging. Conservative treatment is considered as an option if the extratracheal tumour does not grow.
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Affiliation(s)
- Akira Naomi
- Department of Thoracic SurgeryMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Hideyuki Hujiwara
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Tatsuhiko Koizumi
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yukari Sakurai
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yasuo Kohashi
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yukiko Yoneda
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yuka Kitamura
- Department of Thoracic SurgeryMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yoshinobu Hattori
- Department of Thoracic SurgeryMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
| | - Yuji Saitou
- Department of Respiratory MedicineMedical Corporation Kiyosu Respiratory Medical Hospital, Haruhi Respiratory Medical HospitalAchiJapan
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14
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Xia C, Liu M, Niu X, Li X, Chen J. Molecular Features of a Primary Transmural Tracheal Schwannoma: Clinical Experience and Review of the Literature. Cancer Manag Res 2022; 14:1125-1129. [PMID: 35308086 PMCID: PMC8925907 DOI: 10.2147/cmar.s353146] [Citation(s) in RCA: 3] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/08/2021] [Accepted: 02/23/2022] [Indexed: 11/23/2022] Open
Abstract
Primary tracheal schwannoma is a rare disease with no specific symptoms. At the molecular level, neurofibromatosis type 2 (NF2) gene mutation of Schwann cells is the major tumorigenic element. Herein, we present the case of a 54-year-old man with refractory shortness of breath and dry cough, which was resistant to bronchodilator treatment. Computed tomography revealed a transmural mass in the dorsolateral trachea. The tumor was surgically resected, and the diagnosis of schwannoma was confirmed by pathological examination. Furthermore, for this case, we performed whole-exome sequencing and identified several novel mutated schwannoma genes. The specific roles of these mutations need further confirmation.
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Affiliation(s)
- Chunqiu Xia
- Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
| | - Minghui Liu
- Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
| | - Xiaoyu Niu
- Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
| | - Xin Li
- Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
| | - Jun Chen
- Department of Lung Cancer Surgery, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
- Tianjin Key Laboratory of Lung Cancer Metastasis and Tumor Microenvironment, Tianjin Lung Cancer Institute, Tianjin Medical University General Hospital, Tianjin, 300052, People’s Republic of China
- Department of Thoracic Surgery, First Affiliated Hospital, School of Medicine, Shihezi University, Shihezi, Xinjiang, 832008, People’s Republic of China
- Correspondence: Jun Chen; Xin Li, Email ;
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15
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Mohan A, Iyer H, Pahuja S, Barwad A. A rare primary tracheal tumor. Lung India 2022; 39:195-198. [PMID: 35259805 PMCID: PMC9053918 DOI: 10.4103/lungindia.lungindia_972_20] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/12/2022] Open
Abstract
A 20-year-old male without any prior comorbidities presented with 6-month history of hemoptysis as the sole symptom. Clinico-radiological profile and bronchoscopy were suggestive of a tracheal mass. This clinico-pathologic conference discusses the differential diagnoses of primary tumors of the trachea and their management options.
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Wu L, Sha MC, Wu XL, Bi J, Chen ZM, Wang YS. Primary intratracheal neurilemmoma in a 10-year-old girl: A case report. World J Clin Cases 2021; 9:8888-8893. [PMID: 34734071 PMCID: PMC8546825 DOI: 10.12998/wjcc.v9.i29.8888] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/08/2021] [Revised: 07/08/2021] [Accepted: 08/04/2021] [Indexed: 02/06/2023] Open
Abstract
BACKGROUND Tracheal tumors are relatively rare in adults and uncommon in children. Tracheal neurilemmoma is a rare condition in adults that usually affects middle-aged people, but it can also occur in children. Because the clinical presentation is nonspecific and insidious, diagnosis is often delayed. The most common symptoms in these patients are stridor or wheezing (especially positional) and cough. A few patients are misdiagnosed and mistakenly treated for asthma.
CASE SUMMARY A 10-year-old girl was admitted to our unit with a 2-mo history of recurrent cough, dyspnea, and tachypnea. Her condition was more severe after exercise. Her symptoms progressed despite treatment with inhaled fluticasone/salmeterol. Flexible electronic laryngoscopy showed a red, smooth, and round mushroom-shaped mass in the trachea, about 1 cm below the vocal cords. The surface of the mass was covered with several small and discontinuous blood vessels. About 90% of the tracheal lumen was occupied by the mass. A multidisciplinary operation was performed. The surgically resected mass was diagnosed as benign neurilemmoma by immunohistochemical analysis.
CONCLUSION Intratracheal neurilemmoma is fairly rare in children. The main symptoms include coughing, wheezing, and dyspnea. The tumor’s size, location, and degree of intratracheal and extratracheal invasion can be measured by chest computed tomography. The main treatment strategies used for tracheal neurilemmoma are surgical resection and endoscopic excision. Long-term follow-up is warranted for the evaluation of outcomes and complications.
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Affiliation(s)
- Lei Wu
- Department of Pulmonology and Endoscopy Center, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310003, Zhejiang Province, China
| | - Mi-Cun Sha
- Department of Pediatrics, Suqian People’s Hospital of Nanjing Drum-Tower Hospital Group, Suqian 223800, Jiangsu Province, China
| | - Xi-Ling Wu
- Department of Respiratory Medicine, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310002, Zhejiang Province, China
| | - Jing Bi
- Department of Otorhinolaryngology Head and Neck Surgery, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310000, Zhejiang Province, China
| | - Zhi-Min Chen
- Department of Pediatric Pulmonology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310000, Zhejiang Province, China
| | - Ying-Shuo Wang
- Department of Pediatric Pulmonology, The Children’s Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou 310000, Zhejiang Province, China
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Huang HR, Li PQ, Wan YX. Primary intratracheal schwannoma misdiagnosed as severe asthma in an adolescent: A case report. World J Clin Cases 2021; 9:4388-4394. [PMID: 34141805 PMCID: PMC8173418 DOI: 10.12998/wjcc.v9.i17.4388] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.8] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 02/02/2021] [Revised: 03/14/2021] [Accepted: 04/08/2021] [Indexed: 02/06/2023] Open
Abstract
BACKGROUND Primary intratracheal schwannoma is an extremely rare type of benign airway tumor, especially in adolescents. The presenting symptoms are typically prolonged cough and wheezing that can be misdiagnosed as asthma in adolescent patients.
CASE A 16-year-old adolescent girl admitted to a local hospital with symptoms of an irritating cough and wheezing was diagnosed with bronchial asthma and treated with budesonide and formoterol. Over the next year, the patient's wheezing and coughing symptoms gradually worsened and the antiasthma treatment was ineffective. One week prior to this admission, the patient developed dyspnea after catching a cold and was transferred to our hospital with a diagnosis of severe asthma. However, chest computed tomography and bronchoscopy showed a mass in the trachea. Primary intratracheal schwannoma was diagnosed by biopsy. Her symptoms were relieved by endoscopic resection by electrosurgical snaring combined with argon plasma coagulation. No relapse occurred during an 18 mo follow-up.
CONCLUSION Primary intratracheal schwannoma should be considered in the differential diagnosis in adolescents with recurrent asthma-like attacks.
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Affiliation(s)
- Hui-Rong Huang
- Department of Respiratory Medicine, Lanzhou University Second Hospital, Lanzhou 730030, Gansu Province, China
| | - Pei-Qiang Li
- School of Basic Medical Sciences, Lanzhou University, Lanzhou 730000, Gansu Province, China
| | - Yi-Xin Wan
- Department of Respiratory Medicine, Lanzhou University Second Hospital, Lanzhou 730030, Gansu Province, China
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Esch M, Teschner M. Primary tracheal microcystic reticular schwannoma - Case report of a rare neurogenic tumor treated by segmental tracheal resection. Int J Surg Case Rep 2021; 79:251-254. [PMID: 33485177 PMCID: PMC7820791 DOI: 10.1016/j.ijscr.2021.01.016] [Citation(s) in RCA: 4] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/26/2020] [Revised: 01/06/2021] [Accepted: 01/09/2021] [Indexed: 02/05/2023] Open
Abstract
INTRODUCTION AND IMPORTANCE Diagnosis and treatment of rare diseases are challenging because experience and evidence are limited. Primary tracheal tumors have a low prevalence but awareness of these is important to avoid misdiagnoses. We present a first case of a tracheal microcystic reticular schwannoma in which diagnosis and treatment recommendations were revised several times resulting in months of anxious uncertainty for the patient before complete resection and extensive histopathologic examination were performed. CASE PRESENTATION A 65-year old woman complained about coughing and cervical pain. Tomographies revealed a tumor of the dorsolateral trachea. After repeated biopsies pathologists and tumorboards in different hospitals could not agree on diagnosis or treatment recommendation, so the impatient patient opted for a complete resection for definite treatment. CLINICAL DISCUSSION Neoplasms of the posterior mediastinum are mainly neurogenic. In rare cases they may originate in the trachea and can be difficult to differentiate from other tumor entities if only biopsies are available. Although the preoperative diagnosis was unclear, tracheal resection was performed successfully. The differential diagnoses of soft tissue sarcoma or myoepithelioma were discarded and a benign, microcystic, reticular schwannoma was confirmed by international reference pathologists. CONCLUSION Microcystic, reticular schwannoma is a rare variant and may occur in the trachea. Diagnosis of such rare neoplasms can be difficult, resulting in delayed or suboptimal treatment. Often biopsies are not sufficient to reach a definite diagnosis. But even without preoperative histology, tracheal resection is a safe and feasible option for definitive treatment with very low recurrence rates.
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Affiliation(s)
- Matthias Esch
- Klinik für Thoraxchirurgie, Stadtkrankenhaus Delmenhorst, Wildeshauser Str. 92, D-27753 Delmenhorst, Germany.
| | - Martin Teschner
- Klinik für Thoraxchirurgie, Stadtkrankenhaus Delmenhorst, Wildeshauser Str. 92, D-27753 Delmenhorst, Germany.
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Chávez-Fernández DA, Zúñiga-Garza E, López-Saucedo RA. Primary tracheal schwannoma resected in a Turner syndrome patient: a case report. J Surg Case Rep 2020; 2020:rjaa430. [PMID: 33149890 PMCID: PMC7593118 DOI: 10.1093/jscr/rjaa430] [Citation(s) in RCA: 5] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 09/08/2020] [Accepted: 09/28/2020] [Indexed: 11/24/2022] Open
Abstract
We report a case of primary tracheal schwannoma in a 31-year-old woman. She had a previous history of follicular thyroid carcinoma treated surgically and Turner syndrome. In a follow-up computed tomography scan, we found a partially obstructing intraluminal tracheal tumor, which was confirmed by bronchoscopy. The patient was treated by surgical resection and primary tracheal anastomosis. The tumor was 14 mm in diameter, with an intact capsule. Histologic analysis revealed a Schwann cell origin tumor.
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Affiliation(s)
| | - E Zúñiga-Garza
- Surgery Department, Miguel Hidalgo Centennial Hospital, Aguascalientes, Mexico
| | - R A López-Saucedo
- Chair of the Surgery Department/Surgical and Thoracic Oncologist, Miguel Hidalgo Centennial Hospital, Aguascalientes, Mexico
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20
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Zhang L, Tang W, Hong QS, Lv PF, Jiang KM, Du R. Case report: A tracheobronchial schwannoma in a child. Respir Med Case Rep 2020; 30:101047. [PMID: 32346506 PMCID: PMC7182763 DOI: 10.1016/j.rmcr.2020.101047] [Citation(s) in RCA: 5] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/11/2019] [Revised: 03/08/2020] [Accepted: 03/29/2020] [Indexed: 12/14/2022] Open
Abstract
Neurogenic tumors of the tracheobronchial tree are extremely rare, and these include neurofibroma and schwannoma. The rare schwannoma most frequently is reported in adults. We will report an endobronchial schwannoma in an 11-year-old boy.
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Affiliation(s)
- Li Zhang
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
| | - Wen Tang
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
| | - Qing-Shan Hong
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
| | - Pei-Feng Lv
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
| | - Kui-Ming Jiang
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
| | - Rui Du
- Department of Radiology, Guangdong Women and Children Hospital, No. 521 Xingnan Road, Guangzhou, 511400, Guangdong, China
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Chen H, Zhang K, Bai M, Li H, Zhang J, Gu L, Wu W. Recurrent transmural tracheal schwannoma resected by video-assisted thoracoscopic window resection: A case report. Medicine (Baltimore) 2019; 98:e18180. [PMID: 31860964 PMCID: PMC6940164 DOI: 10.1097/md.0000000000018180] [Citation(s) in RCA: 8] [Impact Index Per Article: 1.3] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 02/06/2023] Open
Abstract
RATIONALE Primary schwannoma is extremely rare in the trachea, and its optimal treatment has not yet been established. Previous literature have indicated that traditional resection by thoracotomy is an effective surgical procedure but with huge trauma, and endoscopic excision is a minimally invasive surgical method but with possibility of recurrence. Window resection was usually utilized for selected patients with trachea invasion by thyroid carcinoma, but video-assisted thoracoscopic window resection for trachea schwannoma has not been reported previously. PATIENT CONCERNS A 23-year-old woman was admitted to hospital due to dyspnea, coughing and wheezing that had persisted for 2 months with aggravation for 1 week. DIAGNOSES Chest computed tomography (CT) scan revealed a well-circumscribed soft-tissue mass located on the right lateral posterior wall of the trachea. Bronchofibroscopy (BFS) showed a whitish, smooth and round mass with a wide base in the trachea. Immunohistochemical staining demonstrated cells labeled with Vim (+), S-100 (+), SOX-10 (+), SMA (-), CK (-). Histopathological examinations showed that the mass was a schwannoma. INTERVENTIONS The tumor was nearly completely excised via BFS, but relapsed 2 times at 12 days and 3 weeks after endoscopic resection. Finally, the patient underwent video-assisted thoracoscopic window resection of trachea. OUTCOMES The patient recovered rapidly and no recurrence was observed over 6 months of follow-up. LESSONS The treatment of tracheal schwannoma depends on the characteristics of tumor and the condition of patient. Surgical resection is a preferred alternative for sessile or transmural tumors and recurrence after endoscopic excision. Tracheal window resection by video-assisted thoracoscopy is beneficial for some appropriate patients with a small and sessile tumor.
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Affiliation(s)
- Huiguo Chen
- Department of Cardiothoracic Surgery, the Third Affiliated Hospital, Sun Yat-sen University
| | - Kai Zhang
- Department of Cardiothoracic Surgery, the Third Affiliated Hospital, Sun Yat-sen University
| | - Mingjun Bai
- Department of Vascular Interventional Radiology, the Third Affiliated Hospital, Sun Yat-sen University
| | - Haifeng Li
- Department of Pathology, the Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, People's Republic of China
| | - Jian Zhang
- Department of Cardiothoracic Surgery, the Third Affiliated Hospital, Sun Yat-sen University
| | - Lijia Gu
- Department of Cardiothoracic Surgery, the Third Affiliated Hospital, Sun Yat-sen University
| | - Weibin Wu
- Department of Cardiothoracic Surgery, the Third Affiliated Hospital, Sun Yat-sen University
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22
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Ally M, Kinshuck AJ, Rouhani M, Sandison A, Sandhu GS. The surgical management of recurrent tracheal schwannoma. AME Case Rep 2018; 2:16. [PMID: 30264012 DOI: 10.21037/acr.2018.04.07] [Citation(s) in RCA: 4] [Impact Index Per Article: 0.6] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/01/2018] [Accepted: 04/02/2018] [Indexed: 12/27/2022]
Abstract
A case of a primary tracheal schwannoma refractory to endoscopic treatment in a 54-year-old male is reported. Previous treatment was by endoscopic laser debulking. Computed tomography (CT) 2 months later demonstrated a recurrent tumour involving the anterior tracheal wall with intraluminal tracheal extension. Treatment was successful by limited tracheal resection with primary anastomosis performed 2 weeks following the scan. The histology confirmed a benign neurogenic tumour derived from Schwann cells and clear margins.
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Affiliation(s)
- Munira Ally
- National Centre for Airway Reconstruction, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, UK
| | - Andrew J Kinshuck
- National Centre for Airway Reconstruction, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, UK
| | - Maral Rouhani
- National Centre for Airway Reconstruction, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, UK
| | - Ann Sandison
- Department of Histopathology, Guy's and St Thomas' NHS Foundation Trust, London, UK
| | - Guri S Sandhu
- National Centre for Airway Reconstruction, Charing Cross Hospital, Imperial College Healthcare NHS Trust, London, UK
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23
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Sharma PV, Jobanputra YB, Perdomo Miquel T, Schroeder JR, Wellikoff A. Primary intratracheal schwannoma resected during bronchoscopy using argon plasma coagulation. BMJ Case Rep 2018; 2018:bcr-2018-225140. [PMID: 30232068 DOI: 10.1136/bcr-2018-225140] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/22/2022] Open
Abstract
A 63-year-old man presented with intermittent, progressively worsening dyspnoea associated with cough and blood-tinged sputum. Initial work-up showed left axis deviation on ECG, chest X-ray with an elevated left hemidiaphragm and a non-contrast CT chest that showed a multilobulated mass in the proximal trachea. Bronchoscopy showed a whitish-appearing lesion, which was then sampled and partially resected with pathology showing a schwannoma with no malignant cells. He felt partial relief post procedure; however, he presented a month later with similar symptoms of dyspnoea and a repeat CT scan showed enlargement of the mass in the same location. The patient underwent another flexible bronchoscopy and resection with argon plasma coagulation (APC)/electrocautery snare. APC/electrocautery is an effective interventional bronchoscopy technique that can be used to resect endoluminal lesions or extraluminal lesions that have infiltrated into the airway using flexible/rigid bronchoscopy. It is more cost-effective, safe, works well with vascular lesions and achieves excellent haemostasis as compared with Nd:YAG lasers.
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Affiliation(s)
- Purva V Sharma
- Department of Internal Medicine, University of Miami School of Medicine, Atlantis, Florida, USA
| | - Yash B Jobanputra
- Department of Internal Medicine, University of Miami School of Medicine, Atlantis, Florida, USA
| | | | - J Ryan Schroeder
- Department of Interventional Pulmonology, JFK Medical Center, Atlantis, Florida, USA
| | - Adam Wellikoff
- Department of Interventional Pulmonology, JFK Medical Center, Atlantis, Florida, USA
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24
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Singh A, Pattabhiraman VR, Srinivasan A, Mahadevan S. Dumbbell posterior mediastinal schwannoma invading trachea: Multidisciplinary management - weight off the chest. Lung India 2018; 35:269-272. [PMID: 29697092 PMCID: PMC5946568 DOI: 10.4103/lungindia.lungindia_459_17] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.1] [Reference Citation Analysis] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/17/2023] Open
Affiliation(s)
- Abhijeet Singh
- Department of Interventional Pulmonology and Sleep Medicine, Royal Care Super Speciality Hospital, Coimbatore, Tamil Nadu, India
| | - Vallandramam R Pattabhiraman
- Department of Interventional Pulmonology and Sleep Medicine, Royal Care Super Speciality Hospital, Coimbatore, Tamil Nadu, India
| | - Arjun Srinivasan
- Department of Interventional Pulmonology and Sleep Medicine, Royal Care Super Speciality Hospital, Coimbatore, Tamil Nadu, India
| | - Sivaramakrishnan Mahadevan
- Department of Interventional Pulmonology and Sleep Medicine, Royal Care Super Speciality Hospital, Coimbatore, Tamil Nadu, India
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25
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Choi SM, You JH, Lee SB, Kim SH, Kim YS. A Case of Primary Tracheal Schwannoma. KOSIN MEDICAL JOURNAL 2017. [DOI: 10.7180/kmj.2017.32.2.258] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/11/2022] Open
Abstract
Although benign nerve sheath tumors have been described, primary tracheal schwannomas are extremely rare. We report a case of primary tracheal schwannoma, a rare benign nerve sheath tumor in a 58-year-old man with atypical symptoms of chronic cough, sputum and dyspnea for 2 months. Chest computerized tomography showed a 1.7 cm polypoid lesion in posterior wall of mid trachea. The results of bronchoscopic biopsy and immuno-histo-chemical studies were consistent with schwannoma. A surgical treatment of tumor resection and tracheal reconstruction by end-to-end anastomosis was performed.
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26
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Hamouri S, Novotny NM. Primary tracheal schwannoma a review of a rare entity: current understanding of management and followup. J Cardiothorac Surg 2017; 12:105. [PMID: 29183345 PMCID: PMC5706167 DOI: 10.1186/s13019-017-0677-2] [Citation(s) in RCA: 19] [Impact Index Per Article: 2.4] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/14/2017] [Accepted: 11/22/2017] [Indexed: 02/07/2023] Open
Abstract
BACKGROUND Neurogenic tumors of the tracheobronchial tree are extremely rare and include neurofibroma and schwannoma. We report a case of primary recurrent tracheal schwannoma causing obstructive airway symptoms. CASE PRESENTATION A 60-year-old man presented with obstructive airway symptoms due to recurrent tracheal schwannoma. Due the recurrence, size of the tumor and low surgical risk, the patient was treated with tracheal resection. CONCLUSION Primary endotracheal neurogenic tumors are extremely rare, but one should consider them in the differential diagnosis of persistent upper airway symptoms. While endoscopic therapies recur nearly a quarter of the time, surgical resections do not have any recorded recurrences.
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Affiliation(s)
- Shadi Hamouri
- Department of General Surgery and Urology, Jordan University of Science and Technology, Faculty of Medicine, King Abdullah University Hospital, Irbid, 22110, Jordan.
| | - Nathan M Novotny
- Department of General Surgery and Urology, Jordan University of Science and Technology, Faculty of Medicine, King Abdullah University Hospital, Irbid, 22110, Jordan.,Department of Surgery, Oakland University William Beaumont School of Medicine, Beaumont Health, 3535 W 13 Mile Rd. Ste 307, Royal Oak, MI, 48126, USA
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27
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Dunkman WJ, Nicoara A, Schroder J, Wahidi MM, El Manafi A, Bonadonna D, Giovacchini CX, Lombard FW. Elective Venovenous Extracorporeal Membrane Oxygenation for Resection of Endotracheal Tumor. ACTA ACUST UNITED AC 2017; 9:97-100. [DOI: 10.1213/xaa.0000000000000537] [Citation(s) in RCA: 12] [Impact Index Per Article: 1.5] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/14/2022]
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28
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Saoud M, Patil M, Dhillon SS, Pokharel S, Picone A, Hennon M, Yendamuri S, Harris K. Rare airway tumors: an update on current diagnostic and management strategies. J Thorac Dis 2016; 8:1922-34. [PMID: 27621844 DOI: 10.21037/jtd.2016.07.40] [Citation(s) in RCA: 8] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/21/2022]
Affiliation(s)
- Marwan Saoud
- Department of Medicine, Critical Care and Sleep Medicine, Department of Medicine, State University of New York, Buffalo, New York, USA
| | - Monali Patil
- Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, State University of New York, Buffalo, New York, USA
| | - Samjot Singh Dhillon
- Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, State University of New York, Buffalo, New York, USA;; Department of Medicine, Interventional Pulmonary Section, Roswell Park Cancer Institute, Buffalo, New York, USA
| | - Saraswati Pokharel
- Department of Pathology, Roswell Park Cancer Institute, Buffalo, New York, USA
| | - Anthony Picone
- Department of Thoracic Surgery, Roswell Park Cancer Institute, Buffalo, New York, USA
| | - Mark Hennon
- Department of Thoracic Surgery, Roswell Park Cancer Institute, Buffalo, New York, USA;; Department of Surgery, Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York, USA
| | - Sai Yendamuri
- Department of Thoracic Surgery, Roswell Park Cancer Institute, Buffalo, New York, USA;; Department of Surgery, Jacobs School of Medicine and Biomedical Sciences, Buffalo, New York, USA
| | - Kassem Harris
- Division of Pulmonary, Critical Care and Sleep Medicine, Department of Medicine, State University of New York, Buffalo, New York, USA;; Department of Medicine, Interventional Pulmonary Section, Roswell Park Cancer Institute, Buffalo, New York, USA
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