Massive paraganglioma masquerading as ovarian tumor: a unique case of paraganglioma of undetermined genetic origin.

Q3 Medicine
Baylor University Medical Center Proceedings Pub Date : 2025-01-16 eCollection Date: 2025-01-01 DOI:10.1080/08998280.2024.2448639
Oliver Gibb, Jacob W Lucas, Sujay Deshpande, Daniel C Edwards
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引用次数: 0

Abstract

Paraganglioma and pheochromocytoma are rare tumors originating from chromaffin cells: pheochromocytoma from within the adrenal gland and paraganglioma from the sympathetic chain in the retroperitoneum. Though many are clinically silent, both classically present with hyperadrenergic symptoms. We present a case of a patient with an immense retroperitoneal mass found to be a clinically silent paraganglioma. The unusual size and presentation of the tumor as well as its undetermined genetic origin give a unique perspective into this rare tumor.

伪装成卵巢肿瘤的巨大副神经节瘤:一个独特的遗传来源不明的副神经节瘤病例。
副神经节瘤和嗜铬细胞瘤是起源于嗜铬细胞的罕见肿瘤:嗜铬细胞瘤起源于肾上腺,副神经节瘤起源于腹膜后交感神经链。虽然许多临床无症状,但两者都表现为肾上腺素能亢进症状。我们提出一个病例的病人有一个巨大的腹膜后肿块发现是一个临床沉默副神经节瘤。不寻常的大小和肿瘤的表现,以及其不确定的遗传起源,为这种罕见的肿瘤提供了一个独特的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.30
自引率
0.00%
发文量
245
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