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Horner's syndrome as an unusual complication of retropharyngeal schwannoma excision.
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ENT Department, Nicosia General Hospital, Nicosia, Cyprus.
Synovial sarcoma in the prevertebral space can mimic malignant neurogenic neoplasm: Case report and literature review.
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Department of Radiology, Zhongshan Hospital (Xiamen), Fudan University, Fujian Province, China.
Synovial sarcoma, a rare malignant neoplasm with a poor prognosis, accounts for approximately 5%-10% of all primary soft-tissue malignancies worldwide. Typically affecting adolescents and young adults, it primarily manifests near the joints of the lower extremities. This study aimed to demonstrate that this tumor can also affect the prevertebral space.
View Article and Find Full Text PDFEndoscopic assisted transoral approach with palatal splitting for a giant retropharyngeal schwannoma: a challenging case.
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Department of Otorhinolaryngology, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Retropharyngeal schwannoma is rare. To the best of our knowledge, only 18 cases have been published in the English literature. Complete surgical excision is the treatment of choice for schwannomas.
View Article and Find Full Text PDFRetropharyngeal chordoma extending to the spinal cord, mimicking a neurogenic tumor: a case report and literature review.
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Department of Pathology, Inje University School of Medicine, Busan Paik Hospital, Busan, Republic of Korea.
Chordomas are rare, locally aggressive bone malignancies with poor prognoses. However, those with minimal or no bone involvement are more easily resectable because of their well-delineated margins and thus have better prognoses. Such extraosseous chordomas of the spine are localized both intradurally and extradurally.
View Article and Find Full Text PDFTranstemporal Suprajugular Approach with Neck Dissection for Jugular Foramen Tumor Resection: Operative Video.
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Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, Arizona, United States.
This video demonstrates the transmastoid suprajugular approach with neck dissection to a solitary fibrous tumor involving the jugular foramen and upper cervical region. This patient was a 39-year-old man who presented with dysphagia and cranial nerve (CN) XI and CN XII palsies. Imaging revealed a large homogenously enhancing lesion involving the jugular foramen and extending into the retropharyngeal space ( Fig.
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