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Relevant bibliographies by topics / Paraganglions non chromaffines

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Academic literature on the topic 'Paraganglions non chromaffines'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2025

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Journal articles on the topic "Paraganglions non chromaffines"

1

Talbot, A. R. "Paraganglioma of the maxillary sinus." Journal of Laryngology & Otology 104, no. 3 (1990): 248–51. http://dx.doi.org/10.1017/s002221510011240x.

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AbstractNon-chromaffin paragangliomas are unusual tumours arising in specialized tissue, probably of neural crest origin. A primary non-chromaffin paraganglioma of the paranasal sinuses is a very rare tumour with only a handful of such cases documented in the literature. The presence of such a tumour raises interesting questions as to the origin of such specialized tissue within the nose and paranasal sinuses.

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Ennaoui, Asmaa, Sara Haddougua, Hanane Mourouth, and Youssef Zerrouki. "Anesthetic Management of Unexpected Retroperitoneal Paragonglioma: Case Report." Scholars Journal of Medical Case Reports 11, no. 10 (2023): 1725–28. http://dx.doi.org/10.36347/sjmcr.2023.v11i10.001.

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Paragangliomas are rare tumors that arise from extra-adrenal chromaffine cells. Paraganglioma are classed as functional or non functional based on production of catecholamines, similar pheochromocytoma the clinical presentation is non- specific. We present a case perioperative anesthesic management of accidental intra-operatively diagnosed precave paragonglioma wich was confirmed as pheochromcytoma. A 48 women presented paroxysms of hypertension and adrenergic symptoms including classic triad of episodic headache, sweating, and tachycardia. Abdominal sonography detected an adrenal mass; Surgic

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3

Anas, El Wassi, Bouali Ichrak, Benjelloun Touimi Kenza, et al. "Interduodenal Pancreatic-Caval Tumour Mass: Paraganglioma." European Journal of Medical and Health Research 3, no. 1 (2025): 8–11. https://doi.org/10.59324/ejmhr.2025.3(1).02.

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Non-functional retroperitoneal paragangliomas are rare tumors arising from extraprestinal chromaffin tissue. They are often asymptomatic and can grow to large dimensions, and their diagnosis and surgical management can be difficult. Treatment requires complete surgical excision. We report the case of a 56-year-old patient who presented with epigastric pain. Histological examination of the mass revealed a paraganglioma, a retroperitoneal tumor.

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4

El, Wassi Anas, Ichrak Bouali, Touimi Kenza Benjelloun, et al. "Interduodenal Pancreatic-Caval Tumour Mass: Paraganglioma." European Journal of Medical and Health Research 3, no. 1 (2025): 8–11. https://doi.org/10.59324/ejmhr.2025.3(1).02.

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Non-functional retroperitoneal paragangliomas are rare tumors arising from extraprestinal chromaffin tissue. They are often asymptomatic and can grow to large dimensions, and their diagnosis and surgical management can be difficult. Treatment requires complete surgical excision. We report the case of a 56-year-old patient who presented with epigastric pain. Histological examination of the mass revealed a paraganglioma, a retroperitoneal tumor.

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5

Bıçak, Tuğcem, Selver Özekinci, Yekta Bıçak, and Mansur Dağgülli. "Paraganglioma of Urinary Bladder: A Case Report." Yeni Üroloji Dergisi 18, no. 3 (2023): 258–63. http://dx.doi.org/10.33719/yud.2023;18-3-1287231.

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The majority of bladder lesions are papillary and/or flat-appearing urothelial neoplasms. Neoplasms besides urothelial tumors are very rare. Paragangliomas are rare catecholamine-releasing tumors of sympathetic ganglion or chromaffin cell origin. Approximately 10% of paragangliomas occur in the non-adrenal region, of which 10% are seen in the bladder and constitute 0.05% of all bladder tumors. In a 42-year-old female patient, a 50x43 mm solid mass protruding into the lumen on the left anterolateral aspect of the bladder was observed with necrotic center and increased vascularity on the periphe

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6

Hassan, Muzammil, and Abdul Hafeez Quereshi. "Paraganglioma of the urinary bladder- a case report." Journal of the Pakistan Medical Association 74, no. 4 (2024): 570–72. http://dx.doi.org/10.47391/jpma.8415.

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It is very uncommon to discover Paragangliomas in the urinary bladder. These tumours originate from the sympathetic nerves which supply chromaffin cells in the bladder wall. They can be classified as functional or non-functional. If functional, the most common presentations are with hypertensive crisis or post-micturition syncope. A silent paraganglioma of the bladder can be easily misdiagnosed which can result in severe peri-operative morbidity. We present a case of a male patient who was being managed for hypertension for 2-3 years. He presented at The Indus Hospital, Karachi on 7th August 2

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7

Sengupta, Soumish, Ranjan K. Dey, Abhishek Sati, and Kadambari Ghosh. "Case report on a very rare tumour of the urinary bladder: paraganglioma." International Journal of Advances in Medicine 7, no. 11 (2020): 1753. http://dx.doi.org/10.18203/2349-3933.ijam20204532.

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Urinary bladder tumours are usually of three types; urothelial carcinoma, squamous cell carcinoma and adenocarcinoma. Urothelial carcinoma is the most common type of bladder carcinoma and accounts for almost 90% of all bladder carcinoma. It is also known as transitional cell carcinoma. Squamous cell carcinoma accounts for 4% and adenocarcinomas 2% of all bladder carcinomas. Urinary bladder paragangliomas are a very rare variety of bladder tumours which account for less than 0.06% of all bladder tumours. They are clusters of neuroendocrine cells associated with sympathetic and parasympathetic n

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8

Le, Van Khang, Dang Luu Vu, Thi Ngoc Nguyen, and Thi Thu Hang Nguyen. "LARYNGEAL PARAGANGLIOMA: A CASE REPORT." Vietnamese Journal of Radiology and Nuclear Medicine, no. 4 (December 30, 2024): 49–53. https://doi.org/10.55046/vjrnm.4.1321.2024.

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Paragangliomas correspond to tumors of neuroendocrine origin of chromaffin and non-chromaffin in the paraganglia of thesympathetic or parasympathetic nervous system. Laryngeal and thyroid paragangliomas that arise from the laryngeal paraganglia are extremely rare. Diagnosing two kinds of paragangliomas preoperatively is challenging due to non-specific cytology, pathology, and imaging features, and overlaps with many other neoplasms. Complications in surgery of laryngeal and thyroid paragangliomas may be associated with significant intraoperative bleeding and excision with adherence to nearby s

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9

Ilias, Ioannis, and Karel Pacak. "Developments in Digestive Tract Neuroendocrine Tumors and Pheochromocytomas/Paragangliomas—A Narrative Review." US Endocrinology 07, no. 01 (2011): 59. http://dx.doi.org/10.17925/use.2011.07.01.59.

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Digestive neuroendocrine tumors (carcinoids) derive from serotonin-producing enterochromaffin cells. Biochemical screening (and follow-up) is performed with measurements of 5-hydroxyindoloacetic acid in urine. Other markers are also useful. Most digestive neuroendocrine tumors are better localized with functional imaging, i.e. nuclear medicine, compared with other modalities. The treatment of choice is surgical; non-resectable tumors are treated with somatostatin analogs (unlabelled and for more advanced disease radiolabelled) or chemotherapy. Most pheochromocytomas/paragangliomas are sporadic

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Ilias, Ioannis, and Karel Pacak. "Developments in Digestive Tract Neuroendocrine Tumours and Pheochromocytomas/Paragangliomas – A Narrative Review." European Endocrinology 6, no. 2 (2010): 59. http://dx.doi.org/10.17925/ee.2010.06.02.59.

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Digestive neuroendocrine tumours (carcinoids) derive from serotonin-producing enterochromaffin cells. Biochemical screening (and follow-up) is performed with measurements of 5-hydroxyindoloacetic acid in urine. Other markers are also useful. Most digestive neuroendocrine tumours are better localised with functional imaging, i.e. nuclear medicine, compared with other modalities. The treatment of choice is surgical; non-resectable tumours are treated with somatostatin analogues (unlabelled and for more advanced disease radiolabelled) or chemotherapy. Most pheochromocytomas/paragangliomas are spo

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Dissertations / Theses on the topic "Paraganglions non chromaffines"

1

Csanyi, Michel. "Le paragangliome non-chromaffine de l'orbite : a propos d'un cas et revue de la litterature." Lille 2, 1992. http://www.theses.fr/1992LIL2M311.

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Book chapters on the topic "Paraganglions non chromaffines"

1

Order, Stanley E., and Sarah S. Donaldson. "Chemodectomas (Non-Chromaffin Paragangliomas, GlomusJugulare, Carotid Body Tumors)." In Radiation Therapy of Benign Diseases. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-642-58719-1_29.

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Maher, Eamonn R., and Ruth T. Casey. "Genetics of Phaeochromocytomas, Paragangliomas, and Neuroblastoma." In Oxford Textbook of Endocrinology and Diabetes 3e, edited by John A. H. Wass, Wiebke Arlt, and Robert K. Semple. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780198870197.003.0097.

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Phaeochromocytomas, paragangliomas, and neuroblastomas are the main primary tumours that arise from the autonomic nervous system. The autonomic nervous system is subdivided into the sympathetic and parasympathetic systems. Phaeochromocytomas arise from sympathetic nervous system (chromaffin) cells in the adrenal medulla. Paragangliomas may arise from the sympathetic or parasympathetic system. The former, previously known as extra-adrenal phaeochromocytomas but referred herein as paragangliomas, typically occur along the sympathetic chain and, like phaeochromocytomas, are usually secretory and

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3

"Non-chromaffin Paraganglioma." In Encyclopedia of Otolaryngology, Head and Neck Surgery. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-23499-6_100709.

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