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Relevant bibliographies by topics / Paraganglion

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Academic literature on the topic 'Paraganglion'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2025

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Journal articles on the topic "Paraganglion"

1

McCormack, Sean, Eyad Hamad, and Amar Hamad. "Paraganglioma of the Neck: A Rare Case With Spinal Metastasis." Case Reports in Oncological Medicine 2024 (April 26, 2024): 1–5. http://dx.doi.org/10.1155/2024/2025115.

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Paragangliomas are rare neuroendocrine tumors that arise from the paraganglia, which are clusters of neuroendocrine cells associated with the autonomic nervous system. These tumors are commonly found in the adrenal medulla but can also occur in other locations outside the adrenal gland. Here, we present a case report of a slow-growing paraganglioma in the left neck with spinal metastasis in a 60-year-old man. This case highlights the importance of considering paraganglion tumors in the differential diagnosis of neck masses and the need for early diagnosis and management to prevent potential co

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Thirlwall, A. S., C. M. Bailey, A. D. Ramsay, and M. Wyatt. "Laryngeal paraganglioma in a five-year-old child – the youngest case ever recorded." Journal of Laryngology & Otology 113, no. 1 (1999): 62–64. http://dx.doi.org/10.1017/s0022215100143166.

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AbstractA paraganglioma is a neuroendocrine neoplasm that originates from the paraganglion cells of the parasympathetic system. The average age of presentation is in the fifth decade. We report a case of laryngeal paraganglioma in a five-year-old child, the youngest case ever recorded. The features of paraganglioma which differentiate it from other tumours are also discussed.

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Baker, C., P. Bhagwat, and A. Wan. "Mesenteric paraganglioma with gallbladder paraganglion nest." Journal of Surgical Case Reports 2012, no. 3 (2012): 8. http://dx.doi.org/10.1093/jscr/2012.3.8.

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Blades, Deborah A., Russell W. Hardy, and Mark Cohen. "Cervical paraganglioma with subsequent intracranial and intraspinal metastases." Journal of Neurosurgery 75, no. 2 (1991): 320–23. http://dx.doi.org/10.3171/jns.1991.75.2.0320.

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✓ Paragangliomas, tumors derived from the extra-adrenal paraganglion system, have commonly been found in the retroperitoneum, abdomen, mediastinum, skull base, and neck. Rare intraspinal cases have included involvement of the cauda equina and filum terminale, and a recent case has been reported of thoracic cord paraganglioma with metastasis to the cauda equina. The authors present the case of a patient with a cervical paraganglioma who underwent subtotal resection followed by postoperative irradiation; she subsequently developed multiple intracranial and intraspinal metastases 7 months followi

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Ferrer-Maruland, Eduardo, Diana Paola Urquijo, and Adriana Isaza-Marín. "Primary paraganglioma of the facial nerve: a diagnostic challenge." MOJ Orthopedics & Rheumatology 15, no. 3 (2023): 99–102. http://dx.doi.org/10.15406/mojor.2023.15.00626.

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Paragangliomas are benign tumors of gradual growth that arise from the paraganglion system. They consist of cellular assemblies associated with vascular and neuronal adventitia throughout the body. Moreover, tympanojugular and tympanic PGs are the most common in the head and neck. Primary paraganglioma arising from the facial nerve canal (FN) is rare and challenging to be surgically removed as it is a highly vascularized tumor. Therefore, a preoperative differential diagnosis of an FN tumor is essential for adequate surgical and functional management

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Pfeifer, Johann, and Micheline Gmeiner. "Extraadrenales abdominelles Paraganglion." Colo-Proctology 26, no. 2 (2004): 94–97. http://dx.doi.org/10.1007/s00053-004-5117-9.

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Reddy, C. Ekambar E., Naresh K. Panda, Kim Vaiphei, and Manish Powari. "Pigmented vagal paraganglioma." Journal of Laryngology & Otology 117, no. 7 (2003): 584–87. http://dx.doi.org/10.1258/002221503322113102.

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Paragangliomas are uncommon and those arising from the vagal trunk are rarer. Pigmented extra-adrenal paragangliomas are still rarer and reported sites of occurrence are the uterus, spine, retroperitoneum, bladder, mediastinum and orbit. The presence of abundant pigment in a cervical paraganglion has not been reported previously. We report one such unusual case of pigmented vagal paraganglioma that arose from the vagal trunk below the nodose ganglion, had massive central necrosis and showed hypovascularity on angiography. The unusual features and difficulties in the diagnosis of such cases are

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Bayley, Jean-Pierre, and Peter Devilee. "Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes." Genes 13, no. 6 (2022): 1025. http://dx.doi.org/10.3390/genes13061025.

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Despite two decades of paraganglioma-pheochromocytoma research, the fundamental question of how the different succinate dehydrogenase (SDH)-related tumor phenotypes are initiated has remained unanswered. Here, we discuss two possible scenarios by which missense (hypomorphic alleles) or truncating (null alleles) SDH gene variants determine clinical phenotype. Dysfunctional SDH is a major source of reactive oxygen species (ROS) but ROS are inhibited by rising succinate levels. In scenario 1, we propose that SDH missense variants disrupt electron flow, causing elevated ROS levels that are toxic i

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Madhumita, Mukhopadhyay, Bandopadhyay Binata, Das Chhanda, Ghatak Anannya, Saha Subhamoy, and Kayal Rituparna. "Gastric Neoplasm – A Diagnostic Puzzle." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND BIO-MEDICAL SCIENCE 03, no. 04 (2023): 170–72. https://doi.org/10.5281/zenodo.7837276.

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<strong>Introduction:</strong> Paragangliomas are non-epithelial neuroendocrine tumors originating from neural crest derived paraganglion cells situated in the region of the autonomic nervous system ganglia and accompanying nerves. Very few cases of primary gastric paraganglioma have been reported in the literature till date. We report a rare case of primary gastric paraganglioma. <strong>Case Report:</strong> A 38 year old woman presented with history of melena and dyspepsia. Physical examination revealed mild tenderness in the right hypochondrium, and she was diagnosed to have gall

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Wang, Jeffrey Tzu-Yu, Allen Yu-Yu Wang, Sheila Cheng, Lavier Gomes, and Melville Da Cruz. "Growth Rate Analysis of an Untreated Glomus Vagale on MRI." Case Reports in Otolaryngology 2016 (2016): 1–6. http://dx.doi.org/10.1155/2016/8756940.

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Paragangliomas are slow growing, hypervascular neuroendocrine tumors that develop in the extra-adrenal paraganglion tissues. Paraganglioma involving the vagus nerve ganglia is termed glomus vagale. The slow growth of head and neck paragangliomas especially in the absence of symptom may obviate the necessity for any active intervention, in which case, a “wait and scan” policy is implemented involving long-term clinical and radiologic follow-ups. We present a case of a 71-year-old female with an untreated left glomus vagale who underwent a conservative “wait and rescan” plan of management and th

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Dissertations / Theses on the topic "Paraganglion"

1

Campanucci, Veronica A. Nurse Colin A. "Electrophysiological properties, PO₂- and ATP-sensitivity of paraganglion neurons of the rat glossopharyngeal nerve /." *McMaster only, 2004.

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2

Man, Yang Kee Stella. "Molecular investigations of familial paraganglioma." Thesis, Imperial College London, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.408678.

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Welander, Jenny. "Genetic Alterations in Pheochromocytoma and Paraganglioma." Doctoral thesis, Linköpings universitet, Avdelningen för cellbiologi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-114806.

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Pheochromocytomas and paragangliomas are neuroendocrine tumors that arise from neural crest-derived cells of the adrenal medulla and the extra-adrenal paraganglia. They cause hypertension due to an abnormally high production of catecholamines (mainly adrenaline and noradrenaline), with symptoms including recurrent episodes of headache, palpitations and sweating, and an increased risk of cardiovascular disease. Malignancy in the form of distant metastases occurs in 10-15% of the patients. The malignant cases are difficult to predict and cure, and have a poor prognosis. About a third of pheochro

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Edström, Elder Elisabeth. "Pheochromocytoma and abdominal paraganglioma : clinical and genetic aspects /." Stockholm : [Karolinska institutets bibl.], 2002. http://diss.kib.ki.se/2002/91-7349-116-0/.

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Fliedner, Stephanie [Verfasser]. "Molecular biological characterization of aggressive paraganglioma / Stephanie Fliedner." Magdeburg : Universitätsbibliothek, 2011. http://d-nb.info/1047562006/34.

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Buffet, Alexandre. "Identification de nouveaux gènes de prédisposition aux parangangliomes Positive impact of the knowledge of genetic status on the management and clinical outcome of patients with paraganglioma and/or pheochromocytoma Germline mutations in the mitochondrial 2-oxoglutarate/malate carrier SLC25A11 gene confer a predisposition to metastatic paragangliomas." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCB219.

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Les paragangliomes (PGL) sont des tumeurs neuroendocrines rares, génétiquement déterminées dans 40 % des cas. Malgré les évolutions récentes des connaissances sur la génétique des PGL, il reste toujours environ 15 % des patients pour lesquels aucune cause génétique ne peut être identifiée alors que leur présentation clinique évoque une forme génétiquement déterminée. De plus, il n’a jamais été démontré que l’identification d’une mutation constitutionnelle dans l’un de ces gènes de prédisposition avait un impact positif sur la prise en charge et l’évolution des patients. Mon travail de thèse a

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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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Pillai, Suja. "Genetic Profiling of Phaeochromocytoma and Paraganglioma Using Next Generation Sequencer." Thesis, Griffith University, 2017. http://hdl.handle.net/10072/366446.

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Phaeochromocytoma (PCC) and paraganglioma (PGL) are tumours with neural crest differentiation. They are relatively rare neoplasms, but can be highly malignant, and benign tumours can progress into malignant phenotypes many years after initial diagnosis, a process that is poorly understood. Overall, known genetic mutations account for the pathogenesis of approximately 60% of phaeochromocytoma/paragangliomas. Phaeochromocytoma/paraganglioma are characterised by mutations in twenty-nine specific genes, thus making single gene testing, time consuming and expensive. Next generation sequencing is a

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LIEBAULT, HERBOUILLER CECILE. "Paragangliomes de la tete et du cou : reflexion a propos de trois cas, dont un malin, survenus dans une meme famille." Nantes, 1989. http://www.theses.fr/1989NANT087M.

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VANDORPE, BOUSEMART COLETTE. "Les paragangliomes tympano-jugulaires : aspects cliniques et therapeutiques." Reims, 1991. http://www.theses.fr/1991REIMM052.

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Books on the topic "Paraganglion"

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Wanna, George B., Matthew L. Carlson, and James L. Netterville, eds. Contemporary Management of Jugular Paraganglioma. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-60955-3.

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Wen, Jin, ed. Surgical Management of Pheochromocytoma and Retroperitoneal Paraganglioma. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-8421-3.

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Lack, Ernest E. Pathology of adrenal and extra-adrenal paraganglia. W.B. Saunders, 1994.

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4

Heym, Christine, ed. Histochemistry and Cell Biology of Autonomic Neurons and Paraganglia. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72749-8.

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5

Christine, Heym, and Deutsche Forschungsgemeinschaft, eds. Histochemistry and cell biology of autonomic neurons and paraganglia. Springer-Verlag, 1987.

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6

Andel Gerhard Lourens van der Mey. Head and neck paragangliomas: A clinical genetic and pathological study of glomus tumors. s.n.], 1992.

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1923-, Eyzaguirre Carlos, and International Symposium on Arterial Chemoreceptors (9th : 1988 : Park City, Utah), eds. Arterial chemoreception. Springer-Verlag, 1990.

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8

Grimley, Philip M. Atlas of Tumor Pathology: Tumors of the Extra-Adrenal Paraganglion System. United States Government Printing Office, 1990.

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9

Böck, P. Paraganglia. Springer London, Limited, 2012.

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10

Böck, P. The Paraganglia. Springer, 2011.

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Book chapters on the topic "Paraganglion"

1

Lloyd, Ricardo V. "Extra-Adrenal Paraganglion System." In Endocrine Pathology. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3346-6_9.

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2

Metz, L. "Erfahrungsbericht über die chirurgische Therapie von Tumoren des Paraganglion caroticum." In Sicherheitsaspekte und Qualitätskontrolle in der Gefäßchirurgie Die Lebensqualität des Gefäßpatienten Gefäßmißbildungen und Gefäßtumoren. Steinkopff, 1994. http://dx.doi.org/10.1007/978-3-642-51749-5_21.

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Krmpotić-Nemanić, Jelena, Wolfgang Draf, and Jan Helms. "Paraganglien." In Chirurgische Anatomie des Kopf-Hals-Bereiches. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-11319-6_12.

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Zhai, Qihui “Jim.” "Paraganglioma." In Frozen Section Library. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8612-1_6.

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Debois, J. M. "Paraganglioma." In Selected Topics in Clinical Oncology. Springer Netherlands, 2000. http://dx.doi.org/10.1007/978-94-011-4100-0_2.

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Lin, Lu, and Yining Wang. "Paraganglioma." In Cardiac CT. Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-5305-9_25.

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Rivera, A., and Adekunle M. Adesina. "Paraganglioma." In Atlas of Pediatric Brain Tumors. Springer New York, 2009. http://dx.doi.org/10.1007/978-1-4419-1062-2_23.

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Taverna, Cecilia, and Alessandro Franchi. "Paraganglioma." In Encyclopedia of Pathology. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-28845-1_4873-1.

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Beninato, Toni, and Quan-Yang Duh. "Paraganglioma." In Evidence-Based Endocrine Surgery. Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-1124-5_30.

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Taverna, Cecilia, and Alessandro Franchi. "Paraganglioma." In Encyclopedia of Pathology. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-41894-6_4873.

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Conference papers on the topic "Paraganglion"

1

Blazejczyk, K., and G. Leschber. "Mediastinales Paragangliom – eine chirurgische Herausforderung." In 27. Jahrestagung der Deutschen Gesellschaft für Thoraxchirurgie. Georg Thieme Verlag KG, 2018. http://dx.doi.org/10.1055/s-0038-1668335.

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Geitner, M., and S. Koscielny. "Paragangliom des N. hypoglossus – eine Rarität." In Abstract- und Posterband – 90. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Digitalisierung in der HNO-Heilkunde. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1685731.

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da Rocha, Bruno, Anderson Matsubara, Rodolfo da Rocha, Júlia Goginski, and Ângela Lacerda. "Paraganglioma carotídio: um diagnóstico diferencial." In XXXII Congresso Brasileiro de Neurocirurgia. Thieme Revinter Publicações Ltda, 2018. http://dx.doi.org/10.1055/s-0038-1672776.

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Rosito, Diego. "Lessons Learned in Jugular Paraganglioma Surgery." In 29th Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1679540.

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"Differentially expressed microRNAs in carotid paraganglioma." In Bioinformatics of Genome Regulation and Structure/ Systems Biology. institute of cytology and genetics siberian branch of the russian academy of science, Novosibirsk State University, 2020. http://dx.doi.org/10.18699/bgrs/sb-2020-075.

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Moor, Rachel, Dimitri Laurent, Nichole Allen, et al. "A Rare Case of Clival Paraganglioma." In 31st Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2022. http://dx.doi.org/10.1055/s-0042-1743629.

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Imrisková, E., and P. Jecker. "Sonografische Merkmale von cervikalen Paragangliomen und Neurinomen." In Interdisziplinärer Kongress | Ultraschall 2019 – 43. Dreiländertreffen DEGUM | ÖGUM | SGUM. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1695824.

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Geitner, M., and S. Koscielny. "Paraganglioma of the hypoglossal nerve – a rarity." In Abstract- und Posterband – 90. Jahresversammlung der Deutschen Gesellschaft für HNO-Heilkunde, Kopf- und Hals-Chirurgie e.V., Bonn – Digitalisierung in der HNO-Heilkunde. Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-1685747.

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Gasser, Yvette, Matthew Shrimpton, and Abhishek Malhotra. "3199 Abdominal paraganglioma mimicking idiopathic intracranial hypertension." In ANZAN Annual Scientific Meeting 2024 Abstracts. BMJ Publishing Group Ltd, 2024. http://dx.doi.org/10.1136/bmjno-2024-anzan.151.

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Suresh, Krish, Nicole T. Jiam, Ryan A. Bartholomew, and C. E. Corrales. "Facial Nerve Schwannoma Masquerading as Jugular Paraganglioma." In 33rd Annual Meeting North American Skull Base Society. Georg Thieme Verlag KG, 2024. http://dx.doi.org/10.1055/s-0044-1780229.

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