Results 41 to 50 of about 35,965 (199)
An endotracheal tumour in a 59‐year‐old man with chronic cough and episodic haemoptysis
Key message Endotracheal paraganglioma is a rare disease, with less than 20 cases reported globally. We present images of a patient with endotracheal paraganglioma unveiled following chronic cough and episodic haemoptysis.
Mohammed Amine Bouanzoul
doaj +1 more source
The Impact of Etiology on Time to Vocal Fold Motion Recovery in Unilateral Vocal Fold Paralysis
The time course of vocal fold motion recovery in UVFP reflects the underlying etiologies. This study showed that there was no difference in the time to recovery between UVFP from cardiothoracic versus thyroid/parathyroid surgeries, challenging the long‐held assumption that recovery time is proportional to the distance between injury site and larynx ...
Rishi Suresh, Ted Mau
wiley +1 more source
A rare case of malignant paraganglioma of urinary bladder
Paraganglioma of the urinary bladder is a rare pathologic entity with no definitive histological, immunohistochemical or molecular features to determine its malignant potential. Malignancy is essentially determined by the presence of deep local invasion,
Vinaya B Shah, Amit T Bhandare
doaj +1 more source
Abstract Objective To describe a multidisciplinary protocol for the resection and reconstruction of complex lateral skull base pathology, based on over two decades of experience in a high‐volume tertiary referral center in the United Kingdom. Study Design Retrospective descriptive analysis of institutional practice. Setting A high‐volume tertiary skull
Muhammad Umar Farooq +8 more
wiley +1 more source
Abstract Paragangliomas are rare tumors of the neuroendocrine system that form near certain blood vessels (paraaortic and carotid) and nerves, often presenting heterogeneous parenchyma and displaying strong contrast enhancement on computed tomography.
Romeo Thierry Yehouenou Tessi +3 more
openaire +3 more sources
Abstract Background Pediatric urinary bladder paraganglioma is an exceptionally rare neuroendocrine tumor arising from chromaffin cells within the detrusor muscle. Due to its rarity and variable presentation, early diagnosis can be challenging, often requiring a high index of clinical suspicion and multimodal evaluation.
Shameer Tahir +2 more
wiley +1 more source
The genetics of paragangliomas
Over the last decade, it has been clearly established that one-third of all paragangliomas are genetically determined. Genetic testing, guided by the family history and clinical findings, must now be proposed to all subjects undergoing surgery for head and neck paraganglioma. When a mutation is identified on one of the susceptibility genes (SDHD, SDHB,
Burnichon, N. +4 more
openaire +2 more sources
Intrapericardial paraganglioma [PDF]
We describe the case of an intrapericardial pheochromocytoma located in the anterior surface of the heart and spreading over the pulmonary trunk. Under cardiopulmonary bypass (CPB) the tumor was removed. "En bloc" resection of the anterior wall of the right ventricular infundibulum and the pulmonary trunk was performed, with implantation of a fresh ...
J, Casanova +5 more
openaire +2 more sources
Paraganglioma of Cauda Equina – Case Report
Introduction: Paraganglioma is benign and slow growing neuroectodermal tumor commonly found in the adrenal medulla, carotid body and glomus-jugulare. Paraganglioma of cauda equina is relatively rare.Case Report: We report a case of paraganglioma of the ...
Sushrut M.Fulare +3 more
doaj
Interventional oncology in children: Where are we now?
Abstract Paediatric Interventional Oncology (IO) lags behind adult IO due to a scarcity of specific outcome data. The suboptimal way to evolve this field is relying heavily on adult experiences. The distinct tumour types prevalent in children, such as extracranial germ cell tumours, sarcomas, and neuroblastoma, differ strongly from those found in ...
Premal Amrishkumar Patel +1 more
wiley +1 more source

