Results 71 to 80 of about 5,508 (215)

Laparoscopic management of paraganglioma in a pregnant woman: a case report

International Brazilian Journal of Urology
Introduction: Paraganglioma is an extremely rare catecholamine-producing tumor during pregnancy. Paraganglioma carries high risks of fetal and maternal mortality during pregnancy.
Mohammad Hadi Radfar, Behnam Shakiba, Amir Afyouni, Hassan Hoshyar   +3 more
doaj   +1 more source

Late‐Onset Bone Metastasis 46 Years After Initial Surgery for Pheochromocytoma: A Case Report

IJU Case Reports, Volume 8, Issue 5, Page 533-538, September 2025.
ABSTRACT Introduction Pheochromocytoma is a rare catecholamine‐producing tumor with metastatic potential. Recurrence after more than 40 years is exceptionally rare. Case Presentation During evaluation for ischemic colitis, a 71‐year‐old woman was found to have multiple bone metastases, possibly linked to catecholamine excess.
Fumio Ishizaki, Kaede Hiruma, Yusuke Tani, Hideaki Sugino, Tatsuro Sanami, Tsutomu Anraku, Masahiro Ikeda, Masayuki Tasaki, Kazuhide Saito, Yoshihiko Tomita   +9 more
wiley   +1 more source

Metastatic Malignant Phaeochromocytoma in Ascitic Fluid: Cytological Diagnosis of a Rare Entity

Cytopathology, Volume 36, Issue 5, Page 539-543, September 2025.
In summary, a review of the literature showed that there are only isolated case reports of ruptured pheochromocytoma and to the best of our knowledge this report is the first to document metastatic phaeochromocytoma in peritoneal fluid within the cytopathology literature.
Scarlet Fiona Brockmoeller, Sigfred Lajara, Samer Khader   +2 more
wiley   +1 more source

Primary pulmonary paraganglioma, the unexpected guest of the lung: A case report and literature review

Indian Journal of Pathology and Microbiology
Paragangliomas are rare tumors arising from extra adrenal chromaffin cells. The incidence of primary pulmonary paraganglioma is even less. As new cases are added to the literature, clinical and radiological features become more diverse.
Busra Ozdemir Ciflik, Kadir Baturhan Ciflik, Servet Guresci, Yucel Akkas   +3 more
doaj   +1 more source

Posterior mediastinal paraganglioma with bilateral adrenal pheochromocytoma

, 2004
Paraganglioma and adrenal pheochromocytoma are tumors of common origin arising from chromaffin cells. However, it is extremely rare to find mediastinal paraganglioma simultaneously with bilateral adrenal pheochromocytoma.
Kim, H.J, Lim, S.T, Kim, M.H, Chung, M.J, Kwon, H.J, Jin, G.Y, Lee, Y.C, Park, J.H   +7 more
core   +1 more source

Laparoscopic resection of a large paraganglioma arising in the organ of Zuckerkandl: Report of a case and review of the literature

Journal of Minimal Access Surgery, 2016
Paragangliomas are catecholamine-secreting neuroendocrine tumours arising from chromaffin tissue at extra-adrenal sites. The commonest site for a paraganglioma is the organ of Zuckerkandl.
Hrishikesh Salgaonkar, Ramya Ranjan Behera, Pradeep Chandra Sharma, Manoj Chadha, Avinash N Katara, Deepraj S Bhandarkar   +5 more
doaj   +1 more source

Horner Syndrome Secondary to Suspected Internal Carotid Artery Dissection in a Golden Retriever

Journal of Veterinary Internal Medicine, Volume 39, Issue 5, September/October 2025.
ABSTRACT A 5‐year‐old male golden retriever was presented after a subacute onset of left‐sided Horner syndrome (HS). The dog had anisocoria with left‐sided miosis, ptosis of the upper eyelid, and third eyelid protrusion in the left eye. Because of the absence of additional neurological abnormalities, clinical signs were suggestive of left isolated HS ...
Tommaso Davini, Carlotta Remelli, Chiara Mattei, Swan Specchi, Roberta Biserni, Marco Bernardini   +5 more
wiley   +1 more source

Genetic Testing Referral Rates for Pheochromocytoma and Paraganglioma in an Academic Tertiary Centre

Clinical Endocrinology, Volume 103, Issue 2, Page 147-156, August 2025.
ABSTRACT Background Clinical guidelines recommend genetic counselling for all patients with pheochromocytoma or paraganglioma (PPGL). Barriers to accessing genetics evaluation are incompletely understood. The objective of this study was to identify individual‐ and provider‐level barriers to genetic testing.
Brian Ruhle, Na Eun Kim, Sang Ngo, Elena G. Hughes, Dipti P. Sajed, Run Yu, James X. Wu, Michael W. Yeh, Masha J. Livhits   +8 more
wiley   +1 more source

Management of bladder pheochromocytoma by transurethral resection

Asian Journal of Urology, 2019
Bladder pheochromocytoma is the most common extra-adrenal genitourinary tumor. Endoscopic management is feared due to the risk of intra-operative hypertensive crisis.
Aditya P. Sharma, Girdhar S. Bora, Ravimohan S. Mavuduru, Vikas K. Panwar, Bhagwant R. Mittal, Shrawan K. Singh   +5 more
doaj   +1 more source

Urinary bladder pheochromocytoma managed with TURBT. Case report and review of literature

Urology Case Reports, 2020
Bladder pheochromocytomas are rare catecholamine-secreting tumours of chromaffin cells. Sympathetic system stimulation due to Catecholamine over secretion during micturation is the most common presentation. Unsuspected bladder pheochromocytoma can result
Hassan Alkhatatbeh, Dima Alzaghari, Sufian Alharahsheh, Malik Ayyad   +3 more
doaj   +1 more source