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Steehler AJ, Rothman R, Sadhar B, Saran M, Lipman SP, Lipman RI. Tapia's Syndrome After Cardiac Surgery: A Case Report and Review of Literature. EAR, NOSE & THROAT JOURNAL 2025; 104:29S-38S. [PMID: 35829719 DOI: 10.1177/01455613221113807] [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] [Indexed: 11/17/2022] Open
Abstract
Tapia's syndrome is considered a neuropraxic injury of the recurrent laryngeal nerve and hypoglossal nerve which commonly presents after postoperative general anesthesia as hoarseness and dysphagia. Clinicians should consider this diagnosis in those presenting with symptoms of cranial nerve X and cranial nerve XII injury in the post-extubation setting for prompt diagnosis and management. Here, we report a rare case of Tapia's syndrome following cardiac surgery which was then treated with carboxymethylcellulose gel implant injection.
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Affiliation(s)
- Andrew J Steehler
- Department of Otolaryngology Head and Neck Surgery, University of Pittsburgh Medical Center Hamot, Erie, PA, USA
| | - Ryan Rothman
- Medicine Institute, Allegheny Health Network, Pittsburgh, PA, USA
| | | | - Manick Saran
- Department of Otolaryngology Head and Neck Surgery, University of Pittsburgh Medical Center Hamot, Erie, PA, USA
| | - Sidney P Lipman
- Department of Otolaryngology Head and Neck Surgery, University of Pittsburgh Medical Center Hamot, Erie, PA, USA
| | - Ruthann I Lipman
- Department of Otolaryngology Head and Neck Surgery, University of Pittsburgh Medical Center Hamot, Erie, PA, USA
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Creagh Chapman A, Adshead B, Lovell L, Gorgoraptis N. An Unusual Case of Contralateral Hypoglossal and Recurrent Laryngeal Nerve Palsies Following Endotracheal Intubation. Dysphagia 2024; 39:1213-1217. [PMID: 39162843 DOI: 10.1007/s00455-024-10743-w] [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: 04/11/2024] [Accepted: 07/27/2024] [Indexed: 08/21/2024]
Abstract
We present an unusual case of a 62-year-old male presenting with contralateral hypoglossal and recurrent laryngeal nerve palsies following endotracheal intubation for emergency cardiac surgery. Postoperative, the patient was referred to Speech and Language Therapy due to concerns regarding the safety of his swallow. Oromotor assessment revealed left-sided tongue weakness and aphonia. Flexible endoscopic evaluation of swallowing (FEES) revealed a right vocal cord palsy and severe oropharyngeal dysphagia. There were no other focal neurological signs. An MRI head did not demonstrate a medial medullary stroke or other intracranial lesion. CT neck showed no abnormality identified in relation to the course of the right vagus nerve or recurrent laryngeal nerve at the skull base or through the neck respectively. The patient required a gastrostomy for nutrition and hydration. He continued to be assessed at several month intervals over the course of a year using FEES to obtain a range of voice, secretion and swallowing outcome measures. The patient commenced intensive dysphagia therapy targeting pharyngeal drive, hyolaryngeal excursion and laryngeal sensation. Swallow manoeuvres were trialled during FEES and a head-turn to the side of the vocal cord palsy during deglutition reduced aspiration risk which expedited return to oral intake. The patient had partial recovery over twelve months. Hypoglossal nerve palsy completely resolved. The right vocal cord remained paralysed however the left vocal cord compensated enabling the patient to produce a normal voice. The patient was able to take thin fluids and regular diet and the gastrostomy was removed.
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Affiliation(s)
- Anna Creagh Chapman
- Speech and Language Therapy Department, Royal London Hospital, Barts Health NHS Trust, London, UK.
| | - Briony Adshead
- Speech and Language Therapy Department, Royal London Hospital, Barts Health NHS Trust, London, UK
| | - Lindsay Lovell
- Speech and Language Therapy Department, Royal London Hospital, Barts Health NHS Trust, London, UK
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Perrotta F, Piscopiello D, Iosa G, Gemma D, Rizzo D, De Salvo F, D'Antini D, Scarano E, Colonna F. Bilateral Tapia syndrome in teenager with post traumatic Hangman's fracture and carotid artery dissection. Trauma Case Rep 2024; 51:101029. [PMID: 38633379 PMCID: PMC11021987 DOI: 10.1016/j.tcr.2024.101029] [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] [Accepted: 04/06/2024] [Indexed: 04/19/2024] Open
Abstract
Background Tapia syndrome (TS) is a rare condition characterized by unilateral hypoglossal and recurrent laryngeal nerve palsy, leading to tongue deviation, swallowing difficulty and dysphonia. Case report We describe a case of a 17-year-old boy who reported a bilateral TS following head and neck trauma with Hangman's fracture and right common carotid artery dissection. The confirmation occurred only after complete cognitive and motor recovery, verifying the inability to protrude the tongue and swallow, associated with complete paralysis of the vocal cords, diagnosed with fiber optic laryngoscopy.An initial recovery of tongue motility and phonation occurred after just over a month of rehabilitation. Conclusion In addition to the lack of awareness due to the rarity of the syndrome, the diagnosis of TS may be delayed in patients who are unconscious or who have slow cognitive recovery following head trauma. The case we present may help to increase awareness and avoid unnecessary diagnostic investigations.
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Affiliation(s)
- Francesco Perrotta
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Donato Piscopiello
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Gaetano Iosa
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Daniele Gemma
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Daniela Rizzo
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Francesca De Salvo
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
| | - Davide D'Antini
- Department of Anesthesia and Intensive Care, Azienda Ospedaliera “Cardinale Giovanni Panico”, Tricase, Lecce, Italy
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Piteira R, Marques D, Carrega F, Silvério R, Fera M. Tapia's Syndrome: A Comprehensive Analysis of a Rare Intensive Care-Associated Complication. Cureus 2024; 16:e53486. [PMID: 38314391 PMCID: PMC10838374 DOI: 10.7759/cureus.53486] [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] [Accepted: 02/02/2024] [Indexed: 02/06/2024] Open
Abstract
Tapia's syndrome is a rare complication of airway manipulation, involving the simultaneous paralysis of the hypoglossal nerve and the recurrent laryngeal nerve. The etiological mechanism is commonly attributed to compression or stretching during airway manipulation. An efficient recognition of this condition is pivotal for a comprehensive multidisciplinary approach and optimized recovery time. The presence of persistent dysphagia and dysphonia, coupled with observable deviation or restriction of tongue movement, not only after oral endotracheal intubation for surgical interventions with general anesthesia but also after a prolonged orotracheal intubation period in the intensive care, should heighten the suspicion of this syndrome. This report details a case of Tapia's syndrome emerging as a complication of airway manipulation and prolonged intubation in the intensive care unit.
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Affiliation(s)
- Rita Piteira
- Internal Medicine, Centro Hospitalar de Setúbal, Setúbal, PRT
| | - Diogo Marques
- Neuroradiology, Hospital Garcia de Orta, Almada, PRT
| | - Filipa Carrega
- Internal Medicine, Centro Hospitalar de Setúbal, Setúbal, PRT
| | - Rita Silvério
- Internal Medicine, Centro Hospitalar de Setúbal, Setúbal, PRT
| | - Manuela Fera
- Internal Medicine, Centro Hospitalar de Setúbal, Setúbal, PRT
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Simon CZ, Du JY, Parel P, Adida S, Miller PM, Qureshi S. Hypoglossal and Glossopharyngeal Nerve Palsy After Anterior Cervical Decompression and Fusion: A Case Report. JBJS Case Connect 2024; 14:01709767-202403000-00028. [PMID: 38340356 DOI: 10.2106/jbjs.cc.23.00372] [Citation(s) in RCA: 0] [Impact Index Per Article: 0] [Reference Citation Analysis] [Abstract] [MESH Headings] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 02/12/2024]
Abstract
CASE A 69-year-old man underwent a C3-4 anterior cervical discectomy and fusion and developed postoperative hypoglossal and glossopharyngeal palsies that resolved with symptomatic treatment. CONCLUSION Cranial nerve palsy is a rare and possibly under-reported injury after higher-level cervical spine surgery. Conscientious positioning and awareness of these nerves during surgical exposure are crucial to minimizing cranial nerve palsies. Proper workup to identify these palsies and differentiate them from other complications is necessary to guide proper treatment.
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Affiliation(s)
- Chad Z Simon
- Hospital for Special Surgery, New York City, New York
| | - Jerry Y Du
- Hospital for Special Surgery, New York City, New York
| | - Philip Parel
- Hospital for Special Surgery, New York City, New York
| | - Samuel Adida
- Hospital for Special Surgery, New York City, New York
| | - Payton M Miller
- Division of General Surgery, Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana
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Caranti A, Bianchini C, Corazzi V, Pelucchi S, Ciorba A. Tapia's Syndrome: keep it in mind! Minerva Anestesiol 2022; 88:293-299. [PMID: 35410105 DOI: 10.23736/s0375-9393.21.16037-7] [Citation(s) in RCA: 3] [Impact Index Per Article: 1.0] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 12/21/2022]
Abstract
INTRODUCTION The aim of this study was to revise the etiologic features about Tapia's Syndrome (TS), a condition to particularly consider in the era of the COVID-19 pandemic. EVIDENCE ACQUISITION A systematic review was performed according to the PRISMA criteria. The Medline and Embase databases were searched from January 1, 1990, to December 31, 2020. Initially the search yielded 399 manuscripts, which were reduced to 50, upon the application of inclusion criteria. EVIDENCE SYNTHESIS A total of 65 patients were included in the present review. Mean age was 44±17.5 (DS) years (15-95); M:F ratio was 2.3:1. TS involved mainly the left side (3:2) and was rarely bilateral. Only 2 TS reported cases were due to central causes. Peripheral causes were mainly due to postintubation edema (77%), extrinsic compression (15%), vascular disease (3%), other/not defined (5%). CONCLUSIONS TS is a rare syndrome that has been related to a combined cranial nerve palsy; while TS due to central causes is very rare, it is mainly related to peripheral causes. A particular attention to TS should be given during the SARS-CoV-2 pandemic, either since the correlation between Tapia's syndrome, airway management and anesthetic procedures, since the possible implication of the viral infection itself.
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Affiliation(s)
- Alberto Caranti
- ENT and Audiology Unit, Department of Neurosciences and Rehabilitation, University of Ferrara, Ferrara, Italy -
| | - Chiara Bianchini
- ENT and Audiology Unit, Department of Neurosciences and Rehabilitation, University of Ferrara, Ferrara, Italy
| | - Virginia Corazzi
- ENT and Audiology Unit, Department of Neurosciences and Rehabilitation, University of Ferrara, Ferrara, Italy
| | - Stefano Pelucchi
- ENT and Audiology Unit, Department of Neurosciences and Rehabilitation, University of Ferrara, Ferrara, Italy
| | - Andrea Ciorba
- ENT and Audiology Unit, Department of Neurosciences and Rehabilitation, University of Ferrara, Ferrara, Italy
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Persistent bilateral Tapia syndrome following critical COVID-19. Clin Neurophysiol 2020; 132:505-506. [PMID: 33450570 PMCID: PMC7771298 DOI: 10.1016/j.clinph.2020.12.007] [Citation(s) in RCA: 6] [Impact Index Per Article: 1.2] [Reference Citation Analysis] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Subscribe] [Scholar Register] [Received: 12/18/2020] [Accepted: 12/19/2020] [Indexed: 01/08/2023]
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Waits KD, Kelman CR, Cameron BM. Tapia Syndrome After Cervical Laminoplasty: A Case Report and Review of the Literature. World Neurosurg 2020; 141:162-165. [PMID: 32492536 DOI: 10.1016/j.wneu.2020.05.221] [Citation(s) in RCA: 7] [Impact Index Per Article: 1.4] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/16/2020] [Revised: 05/22/2020] [Accepted: 05/24/2020] [Indexed: 11/16/2022]
Abstract
BACKGROUND Tapia syndrome is a rare complication of surgical positioning with resulting unilateral cranial nerve X and XII deficits that may provide diagnostic challenges in the perioperative period. Timely diagnosis will facilitate obtaining the necessary supportive care while preventing unnecessary workup and procedures. CASE DESCRIPTION The following case report illustrates a patient that developed Tapia syndrome immediately after a posterior cervical laminoplasty with eventual resolution of symptoms. A review of the literature was also undertaken for comparison. CONCLUSIONS Tapia syndrome can occur with a variety of surgeries, but appear to be most common in surgeries of the posterior cervical spine in the neurosurgical literature. It is theorized that flexed head position common among posterior cervical procedures makes patients more prone to Tapia syndrome in these cases. The ideal management remains poorly defined in the literature. The time course and resolution of neurologic deficits support a transient neuropraxic mechanism in most cases, though some patients do suffer permanent deficits.
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Affiliation(s)
- Kevin D Waits
- Department of Neurosurgery, Virginia Commonwealth University Health System, Richmond, Virginia, USA.
| | - Craig R Kelman
- Aspirus Spine and Neurosciences, Aspirus Wausau Hospital, Wausau, Wisconsin, USA
| | - Brian M Cameron
- Department of Neurosurgery, Virginia Commonwealth University Health System, Richmond, Virginia, USA
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Lefevre E, Roblot P, Kalamarides M. Isolated Bilateral Hypoglossal Palsy Complicating a Fourth Ventricle Ependymoma Surgery. World Neurosurg 2020; 140:1-3. [PMID: 32437995 DOI: 10.1016/j.wneu.2020.05.046] [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: 04/18/2020] [Accepted: 05/05/2020] [Indexed: 10/24/2022]
Abstract
BACKGROUND Isolated bilateral hypoglossal palsy is a rare condition that has never been described after surgery in the lower part of the fourth ventricle. In this article, we discuss various possible etiologies and relevant anatomy considerations of the rhomboid fossa. CASE DESCRIPTION We describe a case of bilateral hypoglossal palsy with tongue ptosis following surgery of an ependymoma in the lower part of the fourth ventricle. Immediate postoperative imaging showed ischemic lesions in both hypoglossal nuclei, not compatible with any known arterial territory. Two etiologies could be identified: a venous medullary infarct of the medulla oblongata or direct injury of both hypoglossal nuclei due to their midline position. Finally, the patient improved progressively and returned to normal. CONCLUSIONS Intraoperative neurophysiologic monitoring of hypoglossal nerves, in addition to facial nerves, should be performed for tumors in this location.
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Affiliation(s)
- Etienne Lefevre
- Department of Neurosurgery, APHP, Hôpital de La Pitié-Salpêtrière, Paris, France; Sorbonne Universités, UPMC, Paris, France.
| | - Paul Roblot
- Department of Neurosurgery, APHP, Hôpital de La Pitié-Salpêtrière, Paris, France
| | - Michel Kalamarides
- Department of Neurosurgery, APHP, Hôpital de La Pitié-Salpêtrière, Paris, France; Sorbonne Universités, UPMC, Paris, France
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Brotis AG, Hajiioannou J, Tzerefos C, Korais C, Dardiotis E, Fountas KN, Paterakis K. Bilateral Tapia's syndrome secondary to cervical spine injury: a case report and literature review. Br J Neurosurg 2019:1-5. [PMID: 31096793 DOI: 10.1080/02688697.2019.1617408] [Citation(s) in RCA: 4] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 10/26/2022]
Abstract
A 24-year-old man presented with bilateral Tapia's syndrome (TS) after a traumatic cervical spine injury, manifested by apraxia of the hypoglossal and recurrent laryngeal nerves. The initial presentation was a profound inability to maintain upper respiratory airway patency due to bilateral vocal cord paralysis, accompanied by impairment of swallowing and loss of speech. The diagnosis was based on clinical grounds and verified by endoscopic laryngoscopy. A C7 corpectomy was performed for stabilizing the cervical spine, while conservative treatment with steroids was reserved for the TS. Over the following six months, there was complete resolution of the symptoms.
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Affiliation(s)
- Alexandros G Brotis
- a Department of Neurosurgery , University Hospital of Larissa , Larissa , Greece
| | - Jiannis Hajiioannou
- b Department of Head and Neck Surgery , University Hospital of Larissa , Larissa , Greece.,d Faculty of Medicine , University of Thessaly , Volos , Greece
| | - Christos Tzerefos
- a Department of Neurosurgery , University Hospital of Larissa , Larissa , Greece
| | - Christos Korais
- b Department of Head and Neck Surgery , University Hospital of Larissa , Larissa , Greece
| | - Efthymios Dardiotis
- c Department of Neurology , University Hospital of Larissa.,d Faculty of Medicine , University of Thessaly , Volos , Greece
| | - Kostas N Fountas
- a Department of Neurosurgery , University Hospital of Larissa , Larissa , Greece.,d Faculty of Medicine , University of Thessaly , Volos , Greece
| | - Kostantinos Paterakis
- a Department of Neurosurgery , University Hospital of Larissa , Larissa , Greece.,d Faculty of Medicine , University of Thessaly , Volos , Greece
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11
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Jee CH, Kim HJ, Kwak KH. A case report of Tapia's syndrome after mastectomy and breast reconstruction under general anesthesia. Medicine (Baltimore) 2018; 97:e10980. [PMID: 29851851 PMCID: PMC6392620 DOI: 10.1097/md.0000000000010980] [Citation(s) in RCA: 6] [Impact Index Per Article: 0.9] [Reference Citation Analysis] [Abstract] [Key Words] [MESH Headings] [Track Full Text] [Download PDF] [Figures] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Indexed: 11/25/2022] Open
Abstract
RATIONALE Tapia's syndrome is a rare and potentially anesthesia-related complication that may cause considerable distress to the patient. Here we describe a case of unilateral Tapia's syndrome in a patient undergoing a skin sparing mastectomy and immediate breast reconstruction which, to the best of our knowledge, has not been reported in the literature. PATIENT CONCERNS A 41-years old female underwent right skin sparing total mastectomy and breast reconstruction with latissimus dorsi flap under general anesthesia. On the first postoperative day, she complained left sided tongue deviation, subtle hoarseness and swallowing difficulty. DIAGNOSIS Tapia's syndrome, a combined paralysis of ipsilateral vocal cord and tongue due to injury to the hypoglossal and recurrent laryngeal nerves, in this case, resulting potentially from head and neck position changes INTERVENTIONS:: The patient was closely observed with the administration of empirical prednisolone 5 mg/day for 3 weeks. OUTCOMES One month after the surgery, functions of the tongue and vocal cord were completely resolved. LESSONS Particular attention should be paid to the maintenance of adequate cuff pressure, proper position of endotracheal tube and correct neck positioning, especially when procedures taking a long operation time under endotracheal anesthesia and requiring frequent position changes of the patient's head and neck.
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Affiliation(s)
- Chan hee Jee
- Department of Anesthesiology and Pain Medicine, School of Medicine, Kyungpook National University Hospital
| | - Hyun Jee Kim
- Department of Anesthesiology and Pain Medicine, School of Medicine, Keimyung University
| | - Kyung-Hwa Kwak
- Department of Anesthesiology and Pain Medicine, School of Medicine, Kyungpook National University, Daegu, South Korea
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Bilateral hypoglossal nerve palsy and unilateral recurrent laryngeal nerve palsy following lumbar discectomy: A case report. Eur J Anaesthesiol 2018; 33:464-6. [PMID: 26760406 DOI: 10.1097/eja.0000000000000407] [Citation(s) in RCA: 4] [Impact Index Per Article: 0.6] [Reference Citation Analysis] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 11/26/2022]
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Bilbao I, Dopazo C, Caralt M, Castells L, Pando E, Gantxegi A, Charco R. Isolated bilateral Tapia’s syndrome after liver transplantation: A case report and review of the literature. World J Hepatol 2016; 8:1637-1644. [PMID: 28083087 PMCID: PMC5192556 DOI: 10.4254/wjh.v8.i36.1637] [Citation(s) in RCA: 6] [Impact Index Per Article: 0.7] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Journal Information] [Submit a Manuscript] [Subscribe] [Scholar Register] [Received: 08/19/2016] [Revised: 10/14/2016] [Accepted: 11/02/2016] [Indexed: 02/06/2023] Open
Abstract
AIM To describe one case of bilateral Tapia’s syndrome in a liver transplanted patient and to review the literature.
METHODS We report a case of bilateral Tapia’s syndrome in a 50-year-old man with a history of human immunodeficiency virus and hepatitis C virus child. A liver cirrhosis and a bi-nodular hepatocellular carcinoma, who underwent liver transplantation after general anesthesia under orotracheal intubation. Uneventful extubation was performed in the intensive care unit during the following hours. On postoperative day (POD) 3, he required urgent re-laparotomy due to perihepatic hematoma complicated with respiratory gram negative bacilli infection. On POD 13, patient was extubated, but required immediate re-intubation due to severe respiratory failure. At the following day a third weaning failure occurred, requiring the performance of a percutaneous tracheostomy. Five days later, the patient was taken off mechanical ventilation and severe dysphagia, sialorrea and aphonia revealed. A computerized tomography and a magnetic resonance imaging of the head and neck excluded central nervous injury. A stroboscopy showed bilateral paralysis of vocal cords and tongue and a diagnosis of bilateral Tapia’s syndrome was performed. With conservative management, including a prompt establishment of a speech and swallowing rehabilitation program, the patient achieved full recovery within four months after liver transplantation. We carried out MEDLINE search for the term Tapia’s syndrome. The inclusion criteria had no restriction by language or year but must provide sufficient available data to exclude duplicity. We described the clinical evolution of the patients, focusing on author, year of publication, age, sex, preceding problem, history of endotracheal intubation, unilateral or bilateral presentation, diagnostic procedures, type of treatment, follow-up, and outcome.
RESULTS Several authors mentioned the existence of around 70 cases, however only 54 fulfilled our inclusion criteria. We found only five published studies of bilateral Tapia’s syndrome. However this is the first case reported in the literature in a liver transplanted patient. Most patients were male and young and the majority of cases appeared as a complication of airway manipulation after any type of surgery, closely related to the positioning of the head during the procedure. The diagnosis was founded on a rapid suspicion, a complete head and neck neurological examination and a computed tomography and or a magnetic resonance imaging of the brain and neck to establish the origin of central or peripheral type of Tapia’s syndrome and also the nature of the lesion, ischemia, abscess formation, tumor or hemorrhage. Apart from corticosteroids and anti- inflammatory therapy, the key of the treatment was an intensive and multidisciplinary speech and swallowing rehabilitation. Most studies have emphasized that the recovery is usually completed within four to six months.
CONCLUSION Tapia’s syndrome is almost always a transient complication after airway manipulation. Although bilateral Tapia’s syndrome after general anesthesia is exceptionally rare, this complication should be recognized in patients reporting respiratory obstruction with complete dysphagia and dysarthria after prolonged intubation. Both anesthesiologists and surgeons should be aware of the importance of its preventing measurements, prompt diagnosis and intensive speech and swallowing rehabilitation program.
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Bilateral hypoglossal nerve paralysis following elongated styloid process resection: case report. J Anesth 2016; 30:1082-1086. [PMID: 27544532 DOI: 10.1007/s00540-016-2240-z] [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: 01/20/2016] [Accepted: 08/13/2016] [Indexed: 10/21/2022]
Abstract
We report a case of anesthetic management of a 43-year-old patient with Eagle's syndrome (ES) in whom post-extubation acute airway obstruction occurred due to bilateral hypoglossal nerve paralysis. After an accurate examination, elongated bilateral stylohyoid ligament was observed and surgical resection was planned. After completion of the surgery following extubation, significant dysfunction in swallowing, speech function, and tongue motion was observed. The clinical situation was evaluated as bilateral hypoglossal nerve paralysis related to the procedure. The patient was closely observed over 48 h in the intensive care unit. After 2 days, the patient was discharged to a surgical ward. Following clinical assessment, the patient was discharged from hospital for monthly return. At the 6-month follow-up, there were no further episodes of paresthesia and other symptoms. In conclusion, patients with ES represent a real challenge for physicians from diagnosis to treatment, especially regarding perioperative complications, and close collaboration between surgeons and anesthesiologists is of crucial importance.
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Tapia's syndrome in the intensive care unit: a rare cause of combined cranial nerve palsy following intubation. Acta Neurol Belg 2015; 115:533-7. [PMID: 26088745 DOI: 10.1007/s13760-015-0500-6] [Citation(s) in RCA: 26] [Impact Index Per Article: 2.6] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 04/08/2015] [Accepted: 06/09/2015] [Indexed: 12/31/2022]
Abstract
Tapia's syndrome is characterized by unilateral paralysis of the tongue and vocal cord, and is caused by a concurrent lesion of both the recurrent laryngeal and hypoglossal nerves. The proposed mechanism in most patients is compression or stretching of these nerves on their extracranial course due to airway manipulation under general anaesthesia. As Tapia's syndrome is a rare and possibly devastating condition, recognition of the presence of concurrent paralyses is an important step in diagnosis and treatment. We report two cases of Tapia's syndrome as a complication of intubation in the intensive care unit.
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16
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Shah AC, Barnes C, Spiekerman CF, Bollag LA. Hypoglossal nerve palsy after airway management for general anesthesia: an analysis of 69 patients. Anesth Analg 2015; 120:105-120. [PMID: 25625257 DOI: 10.1213/ane.0000000000000495] [Citation(s) in RCA: 35] [Impact Index Per Article: 3.5] [Reference Citation Analysis] [Abstract] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Indexed: 01/13/2023]
Abstract
Isolated hypoglossal nerve palsy (HNP), or neurapraxia, a rare postoperative complication after airway management, causes ipsilateral tongue deviation, dysarthria, and dysphagia. We reviewed the pathophysiological causes of hypoglossal nerve injury and discuss the associated clinical and procedural characteristics of affected patients. Furthermore, we identified procedural factors potentially affecting HNP recovery duration and propose several measures that may reduce the risk of HNP. While HNP can occur after a variety of surgeries, most cases in the literature were reported after orthopedic and otolaryngology operations, typically in males. The diagnosis is frequently missed by the anesthesia care team in the recovery room due to the delayed symptomatic onset and often requires neurology and otolaryngology evaluations to exclude serious etiologies. Signs and symptoms are self-limited, with resolution occurring within 2 months in 50% of patients, and 80% resolving within 4 months. Currently, there are no specific preventive or therapeutic recommendations. We found 69 cases of HNP after procedural airway management reported in the literature from 1926 to 2013.
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Affiliation(s)
- Aalap C Shah
- From the Department of Anesthesiology and Pain Medicine, University of Washington, Seattle, Washington; and Institute for Translational Health Sciences, University of Washington, Seattle, Washington
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Ghorbani J, Dabir S, Givehchi G, Najafi M. Co-presentation of Tapia's syndrome and pressure alopecia--A rare event after septorhinoplasty: A case report and literature review. ACTA ACUST UNITED AC 2014; 52:38-40. [PMID: 24999217 DOI: 10.1016/j.aat.2014.02.001] [Citation(s) in RCA: 13] [Impact Index Per Article: 1.2] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Journal Information] [Subscribe] [Scholar Register] [Received: 06/01/2013] [Accepted: 09/11/2013] [Indexed: 12/14/2022]
Abstract
Tapia's syndrome and pressure alopecia (PA) are two rare but distressing complications associated with orotracheal intubation and positioning of the head during surgery. To our knowledge, simultaneous occurrence of both complications after surgery has not been previously reported. To avoid these disturbing complications, the mechanisms of the injury and the preventive measures should be recognized by anesthesiologists and surgeons. We herein present the case of Tapia's syndrome together with PA following open septorhinoplasty under uncomplicated endotracheal general anesthesia in a 27-year-old man. We review other case reports and discuss the potential underlying mechanisms of injury.
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Affiliation(s)
- Jahangir Ghorbani
- Department of Otolaryngology Head and Neck Surgery, Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases, Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
| | - Shideh Dabir
- Department of Anesthesiology and Critical Care, Tracheal Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases, Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
| | - Gilda Givehchi
- Department of Otolaryngology Head and Neck Surgery, Amir Alam Hospital, Tehran University of Medical Sciences, Tehran, Iran
| | - Mohammadreza Najafi
- Department of Otolaryngology Head and Neck Surgery, National Research Institute of Tuberculosis and Lung Diseases, Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
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Emohare O, Peterson E, Slinkard N, Janus S, Morgan R. Occam paradox? A variation of tapia syndrome and an unreported complication of guidewire-assisted pedicle screw insertion. EVIDENCE-BASED SPINE-CARE JOURNAL 2014; 4:132-6. [PMID: 24436711 PMCID: PMC3836948 DOI: 10.1055/s-0033-1357355] [Citation(s) in RCA: 3] [Impact Index Per Article: 0.3] [Reference Citation Analysis] [Abstract] [Key Words] [Track Full Text] [Download PDF] [Figures] [Subscribe] [Scholar Register] [Received: 02/21/2013] [Accepted: 07/18/2013] [Indexed: 12/13/2022]
Abstract
Study Design Case report. Clinical Question The clinical aim is to report on a previously unknown association between guidewire-assisted pedicle screw insertion and neuropraxia of the recurrent laryngeal nerve (RLN), and how this may overlap with the signs of Tapia syndrome; we also report our approach to the clinical management of this patient. Methods A 17-year-old male patient with idiopathic scoliosis experienced Tapia syndrome after posterior instrumentation and arthrodesis at the level of T1-L1. After extubation, the patient had a hoarse voice and difficulty in swallowing. Imaging showed a breach in the cortex of the anterior body of T1 corresponding to the RLN on the right. Results Otolaryngological examination noted right vocal fold immobility, decreased sensation of the endolarynx, and pooling of secretions on flexible laryngoscopy that indicated right-sided cranial nerve X injury and left-sided tongue deviation. Aspiration during a modified barium swallow prompted insertion of a percutaneous endoscopic gastrostomy tube before the patient was sent home. On postoperative day 20, a barium swallow demonstrated reduced aspiration, and the patient reported complete resolution of symptoms. The feeding tube was removed, and the patient resumed a normal diet 1 month later. Tapia syndrome, or persistent unilateral laryngeal and hypoglossal paralysis, is an uncommon neuropraxia, which has previously not been observed in association with a breached vertebral body at T1 along the course of the RLN. Conclusion Tapia syndrome should be a differential diagnostic consideration whenever these symptoms persist postoperatively and spine surgeons should be aware of this as a potential complication of guidewires in spinal instrumentation.
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Affiliation(s)
- Osa Emohare
- Center for Spine and Spinal Cord Injury, Regions Hospital, St. Paul, Minnesota, United States ; Department of Orthopaedic Surgery, University of Minnesota, Minneapolis, Minnesota, United States
| | - Erik Peterson
- Center for Spine and Spinal Cord Injury, Regions Hospital, St. Paul, Minnesota, United States
| | - Nathaniel Slinkard
- Department of Orthopaedic Surgery, Henry Ford Health System, Detroit, Michigan, United States
| | - Seth Janus
- Department of Otolaryngology, Regions Hospital, St. Paul, Minnesota, United States ; Department of Otolaryngology, University of Minnesota, Minneapolis, Minnesota, United States
| | - Robert Morgan
- Center for Spine and Spinal Cord Injury, Regions Hospital, St. Paul, Minnesota, United States ; Department of Orthopaedic Surgery, University of Minnesota, Minneapolis, Minnesota, United States
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