Einloggen

Thematische Bibliographien / Extra-adrenal paraganglioma

Inhaltsverzeichnis

Zeitschriftenartikel
Bücher
Buchteile

Auswahl der wissenschaftlichen Literatur zum Thema „Extra-adrenal paraganglioma“

Autor: Grafiati

Veröffentlicht am 7. Juni 2025

Zuletzt aktualisiert am 2. August 2025

Geben Sie eine Quelle nach APA, MLA, Chicago, Harvard und anderen Zitierweisen an

Wählen Sie eine Art der Quelle aus:

Machen Sie sich mit den Listen der aktuellen Artikel, Bücher, Dissertationen, Berichten und anderer wissenschaftlichen Quellen zum Thema "Extra-adrenal paraganglioma" bekannt.

Neben jedem Werk im Literaturverzeichnis ist die Option "Zur Bibliographie hinzufügen" verfügbar. Nutzen Sie sie, wird Ihre bibliographische Angabe des gewählten Werkes nach der nötigen Zitierweise (APA, MLA, Harvard, Chicago, Vancouver usw.) automatisch gestaltet.

Sie können auch den vollen Text der wissenschaftlichen Publikation im PDF-Format herunterladen und eine Online-Annotation der Arbeit lesen, wenn die relevanten Parameter in den Metadaten verfügbar sind.

Zeitschriftenartikel zum Thema "Extra-adrenal paraganglioma"

1

Ramos, Ricard, Juan Moya, Rosa Villalonga, Ricard Morera, and Gerardo Ferrer. "Mediastinal Aortosympathetic Paraganglioma: Report of Two Cases." Asian Cardiovascular and Thoracic Annals 15, no. 4 (2007): e49-e51. http://dx.doi.org/10.1177/021849230701500426.

Der volle Inhalt der Quelle

Annotation:

Thoracic paragangliomas or extra-adrenal pheochromocytomas are uncommon neoplasms that may arise from the extra-adrenal paraganglia. Paragangliomas arising in the anterior mediastinum are most frequent and are related to the base of the heart. Paragangliomas of the posterior mediastinum are most infrequent, and arise from aorticosympathetic paraganglia. We present two cases of posterior mediastinum paraganglioma. Complete tumor resection was done through posterolateral thoracotomy. The diagnosis of aorticosympathectic paraganglioma was established by histologic examination.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

Jaffer, Shabnam, and Noam Harpaz. "Mesenteric Paraganglioma." Archives of Pathology & Laboratory Medicine 126, no. 3 (2002): 362–64. http://dx.doi.org/10.5858/2002-126-0362-mp.

Der volle Inhalt der Quelle

Annotation:

Abstract Approximately 5% to 10% of paragangliomas occur in extra-adrenal sites, which can extend from the upper cervical region to the pelvis, parallel to the autonomic nervous system. This distribution corresponds to the embryologic development of the paraganglia from neural crest cells. Rarely, extra-adrenal paragangliomas can also occur aberrantly outside this distribution. We report such a case of extra-adrenal paraganglioma occurring in the anterior mesentery in a 76-year-old man. Two case reports exist in the literature describing extra-adrenal paragangliomas in the posterior mesentery.

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

Shah, Pinal, Arpita Nishal, Himanshu Patel, Parmita Jayani, and Sheetal Gujrati. "Extra-adrenal Mesenteric Pigmented Paraganglioma: A Rare Case Report." Annals of Pathology and Laboratory Medicine 7, no. 12 (2020): C172–177. http://dx.doi.org/10.21276/apalm.2931.

Der volle Inhalt der Quelle

Annotation:

Paragangliomas are rare neoplasms that arise from neural crest cells of the autonomous system. It has been estimated that 5% to 10% of paragangliomas occur in extra-adrenal sites, which can extend from the upper cervical region to the pelvis, parallel to the autonomic nervous system. This distribution corresponds to the embryologic development of the paraganglia from neural crest cells. Rarely, extra-adrenal paragangliomas can also occur outside this distribution. Herein, we present a case of a 70-year-old female with history of abdominal pain, in whom an abdominal mass was identified during u

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

Tischler, Arthur S. "Pheochromocytoma and Extra-adrenal Paraganglioma: Updates." Archives of Pathology & Laboratory Medicine 132, no. 8 (2008): 1272–84. http://dx.doi.org/10.5858/2008-132-1272-paepu.

Der volle Inhalt der Quelle

Annotation:

Abstract Context.—Advances in genetics and gene expression profiling have led to new ways of thinking about the pathobiology of pheochromocytoma and extra-adrenal paraganglioma. These developments are concurrent with the publication and dissemination of the 2004 World Health Organization bluebook on pathology and genetics of endocrine tumors. Objective.—To summarize new information required by pathologists for effective participation in patient management and research. Data Sources.—Literature review and primary material from Tufts Medical Center. Conclusions.—The World Health Organization res

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Sunita, Kumbhalkar, Archana Aher*, Naik Suprita, and Kumbhalkar Dinkar. "Retroperitoneal paraganglioma presenting as hypertension and paraparesis in young." International Journal of Bioassays 5, no. 09 (2016): 4849. http://dx.doi.org/10.21746/ijbio.2016.09.0011.

Der volle Inhalt der Quelle

Annotation:

Paragangliomas(PGL) are rare tumours that arise from extra-adrenal paraganglia. Extra-adrenal paragangliomas account for only 5 to 10% of all paragangliomas and may present incidentally as a mass. Typical triad of fluctuating hypertension, headache, and sweating is not always present which makes the diagnosis sometimes difficult. Extraadrenal retroperitoneal PGLs are functionally active more often than previously reported and that they are readily detected by soft tissue masses closely associated with the entire length of abdominal aorta. However, no CT feature was found that was unique for PG

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

Wang, Hong-Hau, Yen-Lin Chen, Hao-Lun Kao, et al. "Extra-adrenal paraganglioma of prostate." Canadian Urological Association Journal 7, no. 5-6 (2013): 370. http://dx.doi.org/10.5489/cuaj.1221.

Der volle Inhalt der Quelle

Annotation:

Extra-adrenal pheochromocytomas, or paragangliomas are rare tumors that may develop from extra-adrenal chromaffin cells, and most occur in the organ of Zuckerkandl. Extra-adrenal paraganglioma of the prostate is extremely rare. Here, we report a 53-year-old man with hypertension and lower urinary tract symptoms, who was initially diagnosed as benign prostate hyperplasia. Computed tomography (CT) showed a large heterogenously enhancing mass in the prostate, imprinting the right distal ureter and urinary bladder. Before surgical intervention, CT-guided biopsy of the prostatic mass was performed

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

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.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

Nakao, Yousuke, Yasuo Sakamoto, Yuji Miyamoto, et al. "Laparoscopic Resection of Subclinical Functioning Para-aortic Paraganglioma." International Surgery 104, no. 1-2 (2020): 9–12. http://dx.doi.org/10.9738/intsurg-d-16-00115.1.

Der volle Inhalt der Quelle

Annotation:

Introduction: Extra-adrenal pheochromocytomas (paragangliomas) are neuroendocrine tumors derived from extra-adrenal chromaffin cells. Although laparoscopic resection of adrenal pheochromocytomas is a common procedure, there are few reports of the use of this approach in extra-adrenal para-aortic paragangliomas. Here, we report the case of a patient with a subclinical functioning para-aortic paraganglioma that was successfully resected laparoscopically. Case presentation: A 58-year-old man was referred to our department for treatment of a para-aortic tumor after endoscopic submucosal dissection

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

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.

Der volle Inhalt der Quelle

Annotation:

✓ 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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

Abbasi, Arezou, Kristina M. Wakeman, and Venu G. Pillarisetty. "Pancreatic paraganglioma mimicking pancreatic neuroendocrine tumor." Rare Tumors 12 (January 2020): 203636132098279. http://dx.doi.org/10.1177/2036361320982799.

Der volle Inhalt der Quelle

Annotation:

Extra-adrenal paragangliomas are rare tumors arising from the chromaffin cells of the autonomic nervous system. Retroperitoneal paragangliomas may present as a pancreatic mass. We present a case of a 61-year-old woman with an incidentally found pancreatic mass (7.2 × 6.5 cm) in the CT scan. EUS- guided FNA result was compatible with pancreatic neuroendocrine tumor. Patient underwent pancreaticoduodenectomy and histopathologic assessment revealed the mass was an extra-adrenal paraganglioma. Preoperative diagnosis of pancreatic paragangliomas can be challenging due to imaging and histopathologic

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Mehr Quellen

Bücher zum Thema "Extra-adrenal paraganglioma"

1

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

Den vollen Inhalt der Quelle finden

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

de Krijger, Ronald R., Arthur S. Tischler, Sylvia L. Asa, Ernest E. Lack, and Marco Volante. Tumors of the Adrenal Glands and Extra-Adrenal Paraganglia. American Registry of PathologyArlington, Virginia, 2024. https://doi.org/10.55418/9781933477473.

Der volle Inhalt der Quelle

Annotation:

Abstract The tumors that arise in the adrenals and extra-adrenal paraganglia are not only structurally and hormonally complex, they are also intriguing at the molecular level, where many are recognized as components and harbingers of familial genetic tumor syndromes encompassing a variety of mutations affecting diverse signaling pathways. Building on the foundation laid by the fourth series volume, this fifth series ARP Fascicle summarizes and illustrates the large body of knowledge in this field to provide a comprehensive reference for the clinical, biochemical, radiologic, histologic, immuno

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

Tumors of the Adrenal Gland and Extra-Adrenal Paraganglia: 5f21. ARP Press, 2024.

Den vollen Inhalt der Quelle finden

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

Newell-Price, John, Alia Munir, and Miguel Debono. Adrenal disease. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0188.

Der volle Inhalt der Quelle

Annotation:

This chapter reviews the clinical features, diagnosis, and treatment of three adrenal diseases: adrenal insufficiency, primary aldosteronism (hyperaldosteronism), and phaeochromocytoma. Adrenal insufficiency is a disorder characterized by impaired adrenocortical function. In primary adrenal insufficiency, destruction of the adrenal cortex results in a decreased production of glucocorticoids, mineralocorticoids, and/or androgens. Secondary adrenal insufficiency is due to disordered pituitary and hypothalamic function resulting in decreased secretion of adrenocorticotropic hormone or corticotrop

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Silverberg, Steven G. Tumors of the Uterine Corpus and Gestational Trophoblastic Disease (Atlas of Tumor Pathology 3rd Series). American Registry of Pathology, 1992.

Den vollen Inhalt der Quelle finden

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

Tumors Of The Adrenal Gland & Extra Adrenal Paraganglia (Atlas of Tumor Pathology, Third Series). AMERICAN REGISTRY OF PATHOLOGY, 1997.

Den vollen Inhalt der Quelle finden

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

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

Den vollen Inhalt der Quelle finden

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Buchteile zum Thema "Extra-adrenal paraganglioma"

1

Brennan, Bernadette. "Rare Tumours of the Peripheral Nervous System: Intra-adrenal (Phaeochromocytoma) and Extra-adrenal Paraganglioma." In Pediatric Oncology. Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-92071-5_35.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

2

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.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

3

Tischler, Arthur S., and Ronald R. de Krijger. "Tumors of the Adrenal Medulla and Extra-adrenal Paraganglia." In Surgical Pathology of Endocrine and Neuroendocrine Tumors. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-396-1_9.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

4

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.

Der volle Inhalt der Quelle

Annotation:

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

APA, Harvard, Vancouver, ISO und andere Zitierweisen

5

Maher, Eamonn R., and Ruth T. Casey. "Familial Syndromes and Genetic Causes of Paraganglioma and Phaeochromocytoma." 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/9780198870197.003.0119.

Der volle Inhalt der Quelle

Annotation:

A phaeochromocytoma is a tumour arising from the adrenal medulla and a paraganglioma refers to its extra-adrenal counterpart, which can develop from sympathetic or parasympathetic tissue anywhere from the skull base to the pelvis. Phaeochromocytomas and paragangliomas (PPGL) are considered to be the most heritable tumours as up to 40% of patients who develop these tumours have a hereditary predisposition. This chapter provides an update on the clinical and molecular genetics of PPGL and related syndromes, as well as offering a guideline for genetic testing and surveillance of those individuals

APA, Harvard, Vancouver, ISO und andere Zitierweisen

6

"Familial and Syndrome-Related Pheochromocytoma and Paraganglioma." In Tumors of the Adrenal Glands and Extra-Adrenal Paraganglia. American Registry of PathologyArlington, Virginia, 2024. https://doi.org/10.55418/9781933477473-10.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

7

Rosenow, Edward C. "Carney Triad." In Mayo Clinic Challenging Images for Pulmonary Board Review. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199756926.003.0107.

Der volle Inhalt der Quelle

Annotation:

1. Pulmonary chondroma 2. Gastrointestinal stromal tumor (GIST), formerly, gastric epithelioid leiomyosarcoma 3. Functioning extra-adrenal paraganglioma • Triad eventually present in more than half of patients • 〉90% of patients are female • Mean age: 17 years • Mechanism: unknown (disease absent in 1 identical twin)...

APA, Harvard, Vancouver, ISO und andere Zitierweisen

8

Jouinot, Anne, Fidéline Bonnet-Serrano, and Jérôme Bertherat. "Common Features of Endocrine Tumours." 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/9780198870197.003.0008.

Der volle Inhalt der Quelle

Annotation:

This chapter focuses on endocrine tumours arising from endocrine glands, as defined by the World Health Organization 2017 classification: tumours of the pituitary, the thyroid, the parathyroid, the adrenal cortex, the adrenal medulla, and extra-adrenal paraganglia, and the neuroendocrine pancreas. These tumours share specific features in terms of pathophysiology, diagnosis work-up, and clinical management. Genetic background is frequent and includes genetic predispositions to one specific tumour type, such as pituitary adenoma (AIP), primary bilateral macronodular hyperplasia (ARMC5), or pheoc

APA, Harvard, Vancouver, ISO und andere Zitierweisen

9

Tucci, Marisa, Sergio Lucchini Batista, Silvio Tucci, Jr, et al. "Normotensive Extra-Adrenal Pheochromocytoma Associated with Systemic Amyloidosis — Casual or Causal Association?" In CLINICAL/TRANSLATIONAL - Pheochromocytoma & Paraganglioma. The Endocrine Society, 2011. http://dx.doi.org/10.1210/endo-meetings.2011.part3.p10.p2-637.

Der volle Inhalt der Quelle

APA, Harvard, Vancouver, ISO und andere Zitierweisen

10

Mackenzie, Isla S., and Morris J. Brown. "Phaeochromocytomas, paragangliomas, and neuroblastoma." In Oxford Textbook of Endocrinology and Diabetes. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199235292.003.0554.

Der volle Inhalt der Quelle

Annotation:

Phaeochromocytomas are rare neuroendocrine tumours of neural crest origin, which often produce excess catecholamines (1). Although usually arising from the chromaffin cells of the adrenal medulla, phaeochromocytomas may also arise at other sites of sympathetic or parasympathetic chromaffin tissue anywhere from the base of the skull to the pelvis. Extra-adrenal phaeochromocytomas are called paragangliomas. Some patients with phaeochromocytoma or paraganglioma present with the classical triad of symptoms of headaches, palpitations, and sweating but many others present with less specific features

APA, Harvard, Vancouver, ISO und andere Zitierweisen

Wir bieten Rabatte auf alle Premium-Pläne für Autoren, deren Werke in thematische Literatursammlungen aufgenommen wurden. Kontaktieren Sie uns, um einen einzigartigen Promo-Code zu erhalten!