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Dao V, Chedid I, Shahid P, Sulkowski J, Williams S, Woleben C, Petruzella F, Mahdi E, Urbine J, Vorona G. Rib spur causing a hemothorax, pneumothorax, and diaphragmatic injury in a pediatric patient. Radiol Case Rep 2023; 18:295-299. [PMID: 36388615 PMCID: PMC9649940 DOI: 10.1016/j.radcr.2022.09.075] [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] [Received: 09/16/2022] [Accepted: 09/21/2022] [Indexed: 11/10/2022] Open
Abstract
Pleural effusion is a relatively common condition encountered in the pediatric emergency department. Evaluation of pleural effusion in the emergency department typically includes advanced imaging such as computer tomography or ultrasound, as well as diagnostic thoracocentesis. We report a case of a 10-year-old female with a rib spur at the anterolateral left sixth rib that caused a hemothorax, pneumothorax, and diaphragmatic injury. The patient underwent video-assisted thoracoscopic surgery and resection of the rib spur. The procedure was well-tolerated without any complications.
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Affiliation(s)
- Vinh Dao
- Virginia Commonwealth University School of Medicine, 1201 E Marshall St, Richmond, VA 23298, USA
- Corresponding author.
| | - Imane Chedid
- Department of Pediatric Emergency Medicine, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Peter Shahid
- Department of Radiology, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Jason Sulkowski
- Department of Pediatric Surgery, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Sarah Williams
- Department of Pediatric Emergency Medicine, Inova Fairfax Hospital, 3300 Gallows Rd, Falls Church, VA 22042, USA
| | - Christopher Woleben
- Department of Pediatric Emergency Medicine, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Frank Petruzella
- Department of Pediatric Emergency Medicine, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Eman Mahdi
- Department of Radiology, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Jacqueline Urbine
- Department of Radiology, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
| | - Gregory Vorona
- Department of Radiology, Virginia Commonwealth University Hospital System, 1250 E. Marshall Street, Richmond, VA 23219, USA
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Pan R, Lu X, Wang Z, Duan L, Cao D. Hemothorax caused by costal exostosis injuring diaphragm: a case report and literature review. J Cardiothorac Surg 2022; 17:230. [PMID: 36068632 PMCID: PMC9450418 DOI: 10.1186/s13019-022-01984-7] [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: 06/09/2022] [Accepted: 08/26/2022] [Indexed: 11/25/2022] Open
Abstract
Background Osteochondromas, also known as exostoses, are the most common benign tumors of bone and can be classified into isolated and multiple osteochondromas. A great majority of osteochondromas is asymptomatic, painless, slow-growing mass, and incidentally found. However, osteochondromas occurring in adolescence or in adult patients can grow in size and become symptomatic as a result of mechanical irritation of the surrounding soft tissues or peripheral nerves, spinal cord compression, or vascular injury. Case presentation We present a case of a 13-year-old girl with spontaneous hemothorax, the cause of which was identified by limited thoracotomy with the aid of video-assisted thoracic surgery to be bleeding from a diaphragmatic laceration incurred by a costal exostosis on the left sixth rib. Preoperative chest computed tomography (CT) depicted a bony projection arising from the rib and bloody effusion in the intrathoracic cavity, but was unable to discern the bleeding cause from the lung or the diaphragm. This case will highlight our awareness that costal exostosis possibly results in bloody pleural effusion. Meanwhile, English literatures about solitary costal exostosis associated with hemothorax were searched in PubMed and nineteen case reports were obtained. Combined our present case with available literature, a comprehensive understanding of this rare disease entity will further be strengthened. Conclusions Injury to the diaphragm is the primary cause of hemothorax caused by costal osteochondroma, including the present case. Thoracic CT scan can help establish a diagnosis of preoperative diagnosis of costal osteochondroma. Surgical intervention should be considered for those patients with symptomatic osteochondroma of the rib. Combined with our case and literature, prophylactic surgical removal of intrathoracic exostosis should be advocated even in asymptomatic patients with the presentation of an inward bony spiculation.
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Affiliation(s)
- Ruonan Pan
- Department of Radiology, the First Hospital of Jilin University, No. 71 of Xinmin Street, Changchun, Jilin, 130021, China
| | - Xiaoqian Lu
- Department of Radiology, the First Hospital of Jilin University, No. 71 of Xinmin Street, Changchun, Jilin, 130021, China
| | - Zhijun Wang
- Pediatric Surgery, the First Hospital of Jilin University, Changchun, 130021, China
| | - Lijun Duan
- Department of Radiology, the First Hospital of Jilin University, No. 71 of Xinmin Street, Changchun, Jilin, 130021, China
| | - Dianbo Cao
- Department of Radiology, the First Hospital of Jilin University, No. 71 of Xinmin Street, Changchun, Jilin, 130021, China.
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Computed Tomographic Image Processing and Reconstruction in the Diagnosis of Rare Osteochondroma. COMPUTATIONAL AND MATHEMATICAL METHODS IN MEDICINE 2021; 2021:2827556. [PMID: 34434249 PMCID: PMC8382554 DOI: 10.1155/2021/2827556] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 06/20/2021] [Revised: 07/23/2021] [Accepted: 08/02/2021] [Indexed: 11/17/2022]
Abstract
Objective We applied computed tomography (CT) to explore the imaging manifestations of rare parts of osteochondroma. Based on the medical images, deblurring using a convolutional neural network (CNN), and three-dimensional (3D) reconstruction of the images is performed in order to improve the image diagnosis. Methods Twelve cases of osteochondroma in rare locations confirmed by surgical pathology or clinical long-term dynamic observation were retrospectively analyzed using medical imaging and image reconstruction. There are 7 males and 5 females, with an average age of 43 years. CT examinations were performed in all cases. Image deblurring via the GAN model is performed followed by the 3D reconstruction of the higher quality images is implemented. A retrospective study was performed on the imaging manifestations of the above cases; the imaging characteristics were summarized. Results The imaging features are the following lesions, including 4 cases of the proximal radius, 4 cases of the scapula, 2 cases of the pelvis, and 2 cases of the proximal ribs. The cartilage caps, cortex, and sternum were typical structures of the bone surface of the studied cases. In the continuous imaging features, calcification was visible in some cases, and no significant enhancement was seen in enhanced scans; there was no obvious direction of lesion growth. The image processing techniques that we performed are useful in enhancing the quality of the medical diagnosis. Conclusions Rare site osteochondroma has certain imaging features. In most cases, we can accurately diagnose rare site osteochondroma through these features via the image processing methods that are proposed in this paper.
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Chakravorty A, Fong L, Grant P, Wolfenden H, Akhunji Z. Multiple rib osteochondromas: a rare cause of spontaneous haemothorax. ANZ J Surg 2021; 91:E666-E667. [PMID: 33713535 DOI: 10.1111/ans.16705] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/13/2020] [Revised: 12/10/2020] [Accepted: 02/14/2021] [Indexed: 11/26/2022]
Affiliation(s)
- Ananya Chakravorty
- Department of Cardiothoracic Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia
| | - Laura Fong
- Department of Cardiothoracic Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia
| | - Peter Grant
- Department of Cardiothoracic Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia
| | - Hugh Wolfenden
- Department of Cardiothoracic Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia
| | - Zakir Akhunji
- Department of Cardiothoracic Surgery, Prince of Wales Hospital, Sydney, New South Wales, Australia
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Kanthasamy S, Aresu G, Peryt A, Coonar AS. Surgical Management of Thoracic Multiple Exostoses. Ann Thorac Surg 2019; 109:e361-e362. [PMID: 31589851 DOI: 10.1016/j.athoracsur.2019.08.088] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 07/04/2019] [Revised: 08/15/2019] [Accepted: 08/17/2019] [Indexed: 11/30/2022]
Abstract
Hereditary multiple exostoses is a rare autosomal dominant condition resulting in the development of multiple osteochondromas. We present the case of a 25-year-old woman with hereditary multiple exostoses who was referred for thoracic surgery assessment due to severe right-sided chest pain. Computed tomographic scan allowed preoperative planning for resection of the lesion. Under general anesthesia, right video-assisted thoracoscopic surgery was performed through a cosmetic retromammary incision. Complete removal of the tumor resolved symptoms, and she was discharged 2 days later. We show that video-assisted thoracoscopic surgery with a cosmetically placed muscle-sparing incision allowed accurate resection with faster recovery.
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Affiliation(s)
- Senthooran Kanthasamy
- Department of Thoracic Surgery, Royal Papworth Hospital, Papworth Everard, Cambridge, United Kingdom.
| | - Giuseppe Aresu
- Department of Thoracic Surgery, Royal Papworth Hospital, Papworth Everard, Cambridge, United Kingdom
| | - Adam Peryt
- Department of Thoracic Surgery, Royal Papworth Hospital, Papworth Everard, Cambridge, United Kingdom
| | - Aman S Coonar
- Department of Thoracic Surgery, Royal Papworth Hospital, Papworth Everard, Cambridge, United Kingdom
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Mazza D, Fabbri M, Calderaro C, Iorio C, Labianca L, Poggi C, Turturro F, Montanaro A, Ferretti A. Chest pain caused by multiple exostoses of the ribs: A case report and a review of literature. World J Orthop 2017; 8:436-440. [PMID: 28567348 PMCID: PMC5434351 DOI: 10.5312/wjo.v8.i5.436] [Citation(s) in RCA: 8] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 10/10/2016] [Revised: 12/19/2016] [Accepted: 03/02/2017] [Indexed: 02/06/2023] Open
Abstract
The aim of this paper is to report an exceptional case of multiple internal exostoses of the ribs in a young patient affected by multiple hereditary exostoses (MHE) coming to our observation for chest pain as the only symptom of an intra-thoracic localization. A 16 years old patient with familiar history of MHE came to our observation complaining a left-sided chest pain. This pain had increased in the last months with no correlation to a traumatic event. The computed tomography (CT) scan revealed the presence of three exostoses located on the left third, fourth and sixth ribs, all protruding into the thoracic cavity, directly in contact with visceral pleura. Moreover, the apex of the one located on the sixth rib revealed to be only 12 mm away from pericardium. Patient underwent video-assisted thoracoscopy with an additional 4-cm mini toracotomy approach. At the last 1-year follow-up, patient was very satisfied and no signs of recurrence or major complication had occured. In conclusion, chest pain could be the only symptom of an intra-thoracic exostoses localization, possibly leading to serious complications. Thoracic localization in MHE must be suspected when patients complain chest pain. A chest CT scan is indicated to confirm exostoses and to clarify relationship with surrounding structures. Video-assisted thoracoscopic surgery can be considered a valuable option for exostoses removal, alone or in addiction to a mini-thoracotomy approach, in order to reduce thoracotomy morbidity.
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Sainte S, Decaluwé H, Vanbrabant P. Spontaneous Hemothorax, A Rare Face of Vertebral Osteochondroma. J Emerg Med 2017; 52:e225-e228. [PMID: 28268121 DOI: 10.1016/j.jemermed.2017.01.026] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.1] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 10/30/2016] [Revised: 01/08/2017] [Accepted: 01/22/2017] [Indexed: 11/28/2022]
Abstract
BACKGROUND Osteochondroma is the most common benign tumor of the bone. It is usually asymptomatic, but complications may result from mechanical injury to adjacent anatomic structures, such as the diaphragm and lung, when located intrathoracically. CASE REPORT We report the unusual occurrence of a large hemothorax and lacerated right diaphragm in a 41-year-old woman caused by vertebral osteochondroma affecting the eleventh thoracic vertebra. Thoracoscopic exploration with resection of the osteochondroma and repair of the diaphragm was performed. WHY SHOULD AN EMERGENCY PHYSICIAN BE AWARE OF THIS?: Spontaneous hemothorax is a potential life-threatening condition when the initial diagnosis is postponed and hemodynamic instability and hypovolemic shock occurs. Osteochondroma as a cause of spontaneous hemothorax is uncommon but may require urgent surgical intervention with video-assisted thoracoscopic surgery of thoracotomy to control the hemorrhage and prevent recurrence.
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Affiliation(s)
- Sarah Sainte
- Department of Emergency Medicine, University Hospital Leuven, Leuven, Belgium
| | - Herbert Decaluwé
- Department of Thoracic Surgery, University Hospital Leuven, Leuven, Belgium
| | - Peter Vanbrabant
- Department of Emergency Medicine, University Hospital Leuven, Leuven, Belgium; Department of Internal Medicine, University Hospital Leuven, Leuven, Belgium
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8
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Kadu VV, Saindane KA, Goghate N, Goghate N. Osteochondroma of the Rib: a rare radiological apeareance. J Orthop Case Rep 2016; 5:62-4. [PMID: 27299024 PMCID: PMC4719358 DOI: 10.13107/jocr.2250-0685.258] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Abstract] [Key Words] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/04/2022] Open
Abstract
Introduction: Osteochondromas (exostosis) are the most common neoplasm of bone and arise from the metaphysis of bones. Tumors of the chest wall comprise approximately 2% of all tumors of the body and may be primary or metastatic, benign or malignant. Osteochondroma is a common bone tumor but a rare tumor in the rib. It is often asymptomatic and observed incidentally. The tumors typically begin to grow before puberty and continue until bone maturation is reached. Surgery is required in childhood if these lesions are painful or disfiguring, while those arising in adulthood should always be resected. Case Report: 9 yr old boy presented to OPD with swelling over right chest. Radiograph showed bony outgrowth on the lateral aspect of the 6th rib. The patient was kept under closed observation and was treated conservatively. Three years follow-up didn’t show any increase in the size of the swelling and the patient did not have any complaints. Conclusion: Though various studies have shown that the surgical resection of osteochondroma is necessary to avoid further complications of Haemothorax, pneumothorax or intercostal neuralgia, we concluded that osteochondroma of the ribs can even be conserved if not associated with complications and patient does not need to undergo unnecessary surgery.
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Affiliation(s)
- Vikram V Kadu
- ACPM Medical College, Dhule - 424001, Maharashtra. India
| | - K A Saindane
- ACPM Medical College, Dhule - 424001, Maharashtra. India
| | - Ninad Goghate
- ACPM Medical College, Dhule - 424001, Maharashtra. India
| | - Neha Goghate
- ACPM Medical College, Dhule - 424001, Maharashtra. India
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Kameda T, Makino T, Sakai T, Koezuka S, Otsuka H, Hata Y, Tochigi N, Shibuya K, Iyoda A. Asymptomatic costal exostosis with thickening in the pericardium: a case report. J Cardiothorac Surg 2016; 11:36. [PMID: 26946299 PMCID: PMC4779563 DOI: 10.1186/s13019-016-0431-1] [Citation(s) in RCA: 5] [Impact Index Per Article: 0.6] [Reference Citation Analysis] [Abstract] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 08/07/2015] [Accepted: 02/29/2016] [Indexed: 02/08/2023] Open
Abstract
Background Costal exostosis is a benign condition that sometimes requires emergent surgery because of associated hemothorax; in addition, there have been cases with malignant transformation to chondrosarcoma. Here, we describe an asymptomatic patient who underwent thoracoscopic resection for primary costal exostosis. Case presentation A 16-year-old male was found to have a bow-shaped shadow on a chest X-ray. Chest computed tomography revealed a rod-like mass with a soft tissue shadow adjacent to the left fifth rib. A thoracoscopic partial resection of the left fifth rib was performed. Intraoperative findings included thickening of the pericardium near the tip of the growth and erosion of the visceral pleura of the left lung. The resected specimen was diagnosed as a primary costal exostosis based on histopathological findings. Conclusions We review the published literature on costal exostosis and discuss the surgical indications of asymptomatic cases.
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Affiliation(s)
- Toru Kameda
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Takashi Makino
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Takamitsu Sakai
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Satoshi Koezuka
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Hajime Otsuka
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Yoshinobu Hata
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
| | - Naobumi Tochigi
- Department of Surgical Pathology, Toho University School of Medicine, Tokyo, Japan.
| | - Kazutoshi Shibuya
- Department of Surgical Pathology, Toho University School of Medicine, Tokyo, Japan.
| | - Akira Iyoda
- Division of Chest Surgery, Toho University School of Medicine, Tokyo, Japan.
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10
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Osteochondroma of the fifth rib resulting in recurrent hemothorax. Skeletal Radiol 2015; 44:1853-6. [PMID: 26424661 DOI: 10.1007/s00256-015-2257-7] [Citation(s) in RCA: 1] [Impact Index Per Article: 0.1] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 06/26/2015] [Revised: 08/10/2015] [Accepted: 09/14/2015] [Indexed: 02/02/2023]
Abstract
A 48-year-old man presented with recurrent spontaneous hemothoraces, which ultimately were found to be secondary to a pedunculated costal osteochondroma causing vascular injury. After initially undergoing endovascular coil embolization, he ultimately required segmental rib resection containing the offending lesion for definite treatment. Although a few cases of symptomatic costal osteochondromas have been reported in the literature, as far as we know, no previous reports have provided direct radiologic confirmation of active bleeding or the role of angiographic intervention. In this report, we highlight the importance of CT angiography in establishing a direct link between an osteochondroma and recurrent hemothorax. We also discuss the diagnostic imaging challenges associated with this condition and the use of a multidisciplinary treatment strategy involving both angiographic and operative management.
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Rodrigues JCL, Mathias HC, Lyen SM, Mcalindon E, Bucciarelli-Ducci C, Batchelor TJP, Hamilton MCK, Manghat NE. A Novel Cause of Acute Coronary Syndrome Due to Dynamic Extrinsic Coronary Artery Compression by a Rib Exostosis: Multimodality Imaging Diagnosis. Can J Cardiol 2015; 31:1303.e9-1303.e11. [PMID: 26255213 DOI: 10.1016/j.cjca.2015.05.008] [Citation(s) in RCA: 6] [Impact Index Per Article: 0.6] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 05/05/2015] [Revised: 05/08/2015] [Accepted: 05/08/2015] [Indexed: 12/12/2022] Open
Abstract
We report a case of acute coronary syndrome secondary to intermittent extrinsic compression of the left anterior descending coronary artery by inward-pointing rib exostosis in an 18-year-old woman during forceful repeated expiration in labour. The diagnosis was achieved using multimodality noninvasive cardiac imaging. In particular, we demonstrated the novel role of expiratory-phase cardiac computed tomography in confirming the anatomical relationship of the bony exostosis to the left anterior descending coronary artery. The case reminds us the heart and mediastinum move dynamically, relative to the bony thorax, throughout the respiratory cycle, and that changes in cardiac physiology in pregnancy may become pathological.
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Affiliation(s)
- Jonathan C L Rodrigues
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom; Department of Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom.
| | - Helen C Mathias
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom; Department of Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Stephen M Lyen
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom; Department of Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Elisa Mcalindon
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Chiara Bucciarelli-Ducci
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Timothy J P Batchelor
- Department of Thoracic Surgery, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Mark C K Hamilton
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom; Department of Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
| | - Nathan E Manghat
- NIHR Bristol Cardiovascular Biomedical Research Unit, Bristol Heart Institute, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom; Department of Radiology, Bristol Royal Infirmary, University Hospitals Bristol NHS Foundation Trust, Bristol, United Kingdom
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Non-traumatic and spontaneous hemothorax in the setting of forensic medical examination: a systematic literature survey. Forensic Sci Int 2013; 236:22-9. [PMID: 24529771 DOI: 10.1016/j.forsciint.2013.12.013] [Citation(s) in RCA: 14] [Impact Index Per Article: 1.2] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 03/21/2013] [Revised: 12/07/2013] [Accepted: 12/15/2013] [Indexed: 01/18/2023]
Abstract
Spontaneous hemothorax is a well-known yet seldom-reported entity in forensic literature. While trauma-related hemothorax is frequently encountered in a medicolegal setting, non-traumatic and spontaneous hemothorax are relatively uncommon entities. The wide range of causes that can trigger fatal intrathoracic bleeding include thoracic aortic dissection, followed by vascular malformations, various oncological diseases, and connective tissue abnormalities. In rare instances, extramedullary hematopoiesis, ectopic pregnancy, congenital heart defects, amyloidosis, or parasitic diseases may constitute a source of bleeding. This etiological heterogeneity may, as a result, cause diagnostic difficulties during post-mortem elucidation of hemothorax. It should be borne in mind that hemothorax after low-energy trauma does not exclusively indicate traumatic hemorrhage, hence, the non-traumatic origin of bleeding must be taken into consideration. In this paper, we present a systematic review of the relevant literature enriched by the results of our observations to investigate the etiologies and recommendations for the post-mortem diagnosis of spontaneous hemothorax in an attempt to better delineate the possible medicolegal considerations. It is important that forensic pathologist as well as clinicians are aware of the diseases that could potentially give rise to fatal hemothorax.
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13
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Huang L, Lu Q, Yan X, Han Y. A 5-year-old boy with a large hereditary multiple exostoses lump grown into thoracic cavity. Ann Thorac Cardiovasc Surg 2013; 20 Suppl:528-30. [PMID: 23364238 DOI: 10.5761/atcs.cr.12.01989] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/16/2022] Open
Abstract
Multiple exostosis is associated with the autosomal dominant disorder and hereditary multiple exostoses (HMEs), are rarely growing around the ribs and the formation of a large lump into the thoracic cavity. It's generally agreed that when there are no symptoms present, a HME patient could either avoid any treatment or postpone the operation until adolescence. We present a 5-year-old boy with 4 cm × 3.5 cm HMEs lump invasion into the thoracic cavity, with symptoms of chest distress and right chest pain. This patient received video-assisted thoracoscopic surgery (VATS) and a the lump and 1 cm rib involved was resected. During a 2 years follow-up, the patient remained in good condition without recurrence and complications.
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Affiliation(s)
- Lijun Huang
- Department of Thoracic Surgery, Tangdu Hospital, Fourth Military Medical University, Xi'an, China
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Imai K, Suga Y, Nagatsuka Y, Usuda J, Ohira T, Kato H, Ikeda N. Pneumothorax caused by costal exostosis. Ann Thorac Cardiovasc Surg 2012; 20:161-4. [PMID: 23269261 DOI: 10.5761/atcs.cr.12.01955] [Citation(s) in RCA: 15] [Impact Index Per Article: 1.2] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/01/2023] Open
Abstract
Exostosis occurs in the ribs either sporadically or as a manifestation of a genetic disorder known as hereditary multiple exostoses. Costal exostosis may cause chest pain and, on rare occasions, result in hemothorax, pneumothorax, hemopneumothorax, and diaphragmatic or pericardial laceration. We report a case of pneumothorax in a 16-year-old boy with exostosis in the right seventh and eighth ribs. He previously received a diagnosis of multiple exostoses and underwent costal resection. The lung and pleura were injured because of long-term friction between the exostoses and the visceral pleura.To the best of our knowledge, this is only the fourth report of pneumothorax caused by costal exostosis. Moreover, all previously reported cases of pneumothorax or hemopneumothorax caused by costal exostosis, including the present case, involved lower lobe injury.
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Affiliation(s)
- Kentaro Imai
- Department of Thoracic Surgery, Tokyo Medical University, Tokyo, Japan
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15
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Nakano T, Endo S, Tsubochi H, Tetsuka K. Thoracoscopic findings of an asymptomatic solitary costal exostosis: is surgical intervention required? Interact Cardiovasc Thorac Surg 2012; 15:933-4. [PMID: 22914805 DOI: 10.1093/icvts/ivs374] [Citation(s) in RCA: 6] [Impact Index Per Article: 0.5] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/19/2022] Open
Abstract
We report a case of a 21-year old male with an asymptomatic solitary costal exostosis incidentally detected on a chest X-ray. The exostosis originated from the costochondral junction of the left fourth rib and protruded into the thoracic cavity. Exploratory thoracoscopy showed that the exostosis had scratched the adjacent pericardium and visceral pleura. A 5.5-cm long rib segment including the exostosis was excised. This report describes that the thoracoscopic findings of an asymptomatic costal exostosis originate from the costochondral junction, demonstrating that this condition may cause more extensive thoracic organ injury than expected.
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Affiliation(s)
- Tomoyuki Nakano
- Department of General Thoracic Surgery, Jichi Medical University Saitama Medical Center, Saitama, Japan.
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Cheng PG, Chen CC, Wu SK, Hsu SM, Wang MN. Thorn-like costal osteochondroma presenting as hemothorax in an adult. FORMOSAN JOURNAL OF SURGERY 2012. [DOI: 10.1016/j.fjs.2012.01.005] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/17/2022] Open
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17
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Vemula R, Shah S, Willekes II LJ. Unusual Case of Pneumothorax Caused by Costal Osteochondroma. ACTA ACUST UNITED AC 2012. [DOI: 10.4236/ojts.2012.24022] [Citation(s) in RCA: 2] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/15/2023]
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Mann E, Kaafarani HM, Cassidy C, Chwals WJ, Jackson CC. Spontaneous Hemothorax in Multiple Exostoses: A Case Report and Review of Literature. J Laparoendosc Adv Surg Tech A 2011; 21:575-7. [DOI: 10.1089/lap.2010.0494] [Citation(s) in RCA: 13] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/17/2022] Open
Affiliation(s)
- Elizabeth Mann
- Tufts University School of Medicine, Boston, Massachusetts
| | - Haytham M.A. Kaafarani
- Tufts University School of Medicine, Boston, Massachusetts
- Division of Pediatric Surgery, Floating Hospital for Children at Tufts Medical Center, Boston, Massachusetts
| | - Charles Cassidy
- Tufts University School of Medicine, Boston, Massachusetts
- Department of Orthopedics, Tufts Medical Center, Boston, Massachusetts
| | - Walter J. Chwals
- Tufts University School of Medicine, Boston, Massachusetts
- Division of Pediatric Surgery, Floating Hospital for Children at Tufts Medical Center, Boston, Massachusetts
| | - Carl-Christian Jackson
- Tufts University School of Medicine, Boston, Massachusetts
- Division of Pediatric Surgery, Floating Hospital for Children at Tufts Medical Center, Boston, Massachusetts
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Oudyi M, David M, Blondel B, Bosdure E, Gorincour G, Launay F, Dubus JC. Hémothorax et maladie exostosante multiple héréditaire chez un enfant de 9 ans. Arch Pediatr 2011; 18:170-5. [PMID: 21190817 DOI: 10.1016/j.arcped.2010.11.009] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.2] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 02/25/2010] [Revised: 07/07/2010] [Accepted: 11/25/2010] [Indexed: 01/01/2023]
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Khosla A, Parry RL. Costal osteochondroma causing pneumothorax in an adolescent: a case report and review of the literature. J Pediatr Surg 2010; 45:2250-3. [PMID: 21034955 DOI: 10.1016/j.jpedsurg.2010.06.045] [Citation(s) in RCA: 28] [Impact Index Per Article: 1.9] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 04/14/2010] [Revised: 06/23/2010] [Accepted: 06/25/2010] [Indexed: 02/08/2023]
Abstract
Costal osteochondroma is a rare but important condition to recognize because of the possibility of serious consequences if not diagnosed and treated promptly. Patients can present with numerous complications, including hemothorax, pneumothorax, nervous or vascular impingement, and fracture. We report the case of a 17-year-old adolescent boy who presented to the pediatrician with intermittent shortness of breath and pleuritic chest pain. A chest x-ray demonstrated a left-sided pneumothorax and triangular opacity in the left chest. A computed tomographic scan of the chest revealed the cause to be a costal exostosis of the anterior fifth rib. The lesion was excised using video-assisted thoracoscopic surgery, which has become an increasingly popular method for treating these lesions, causing significantly less morbidity and allowing for a faster recovery than a major thoracotomy.
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Affiliation(s)
- Arjun Khosla
- Division of Pediatric Surgery, Rainbow Babies and Children's Hospital, Case Western Reserve University, Cleveland, OH 44106, USA.
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Takata K, Suzuki K, Kurosaki Y. Spontaneous hemothorax in hereditary multiple exostosis involving the ribs. ACTA ACUST UNITED AC 2008; 26:39-41. [DOI: 10.1007/s11604-007-0186-7] [Citation(s) in RCA: 14] [Impact Index Per Article: 0.8] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 01/05/2007] [Accepted: 08/23/2007] [Indexed: 11/30/2022]
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Pham-Duc ML, Reix P, Mure PY, Pracros JP, Moreux N, Bellon G. Hemothorax: an unusual complication of costal exostosis. J Pediatr Surg 2005; 40:e55-7. [PMID: 16291144 DOI: 10.1016/j.jpedsurg.2005.07.060] [Citation(s) in RCA: 20] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 02/07/2023]
Abstract
We report a case of a spontaneous hemothorax in a 15-year-old girl because of costal exostosis. This possibly may have been provoked by a nontraumatic rupture of markedly dilated pleural vessels because of long-standing friction between the exostosis and the pleura. The authors conclude that exostosis of the rib is a rare cause of hemothorax in children and should be considered among possible etiologies in diagnosis.
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Affiliation(s)
- Mai Linh Pham-Duc
- Department of Pediatrics, Pulmonology, Allergology and Cystic Fibrosis, Hôpital Debrousse, 69322 Lyon, France
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Cowles RA, Rowe DH, Arkovitz MS. Hereditary multiple exostoses of the ribs: an unusual cause of hemothorax and pericardial effusion. J Pediatr Surg 2005; 40:1197-200. [PMID: 16034772 DOI: 10.1016/j.jpedsurg.2005.03.064] [Citation(s) in RCA: 33] [Impact Index Per Article: 1.7] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 12/19/2022]
Abstract
A 6-year-old girl with hereditary multiple exostoses presented with spontaneous hemothorax and pericardial effusion. Chest computed tomographic scan showed left-sided costal exostoses protruding into the left side of the chest. She underwent successful thoracoscopic resection of 3 left rib exostoses and made a full recovery. This report illustrates this rare clinical scenario and reviews the previously published reports of this complication of costal exostoses.
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Affiliation(s)
- Robert A Cowles
- Division of Pediatric Surgery, The Children's Hospital of New York-Presbyterian, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA
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Jin W, Hyun SY, Ryoo E, Lim YS, Kim JK. Costal osteochondroma presenting as haemothorax and diaphragmatic laceration. Pediatr Radiol 2005; 35:706-9. [PMID: 15806405 DOI: 10.1007/s00247-005-1407-9] [Citation(s) in RCA: 17] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 12/03/2004] [Accepted: 12/13/2004] [Indexed: 12/19/2022]
Abstract
We report the unusual case of an 11-year-old girl who suffered a large haemothorax and lacerated left hemidiaphragm because of a costal osteochondroma arising from the left sixth rib near the costochondral junction. Surgical excision of the osteochondroma was performed and the lacerated diaphragm was repaired.
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Affiliation(s)
- Wook Jin
- Department of Diagnostic Radiology, Gil Medical Centre, Gachon Medical School, 1198 Guweol-dong, Namdong-gu, Incheon, South Korea.
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Abstract
We report two cases of unusual presentation of rib exostosis. The first patient presented acutely with hemorrhagic shock due to massive hemothorax, and the second patient presented with repetitive chest infection complicated by empyema. In both patients, preoperative computed tomographic (CT) scan of the chest revealed rib exostoses, necessitating thoracotomy and rib resection.
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Affiliation(s)
- Waseem M Hajjar
- Department of Surgery, Division of Thoracic Surgery, King Khalid University Hospital, Riyadh, Saudi Arabia
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Abstract
This report describes a 21-year-old man who presented with pericardial hemorrhage due to a puncture wound of the pericardium by an inward-facing exostosis of the left fifth rib.
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Affiliation(s)
- Ichiro Fukai
- The Second Department of Surgery, Nagoya City University Medical School, Nagoya, Japan.
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