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伪装成卵巢肿瘤的巨大副神经节瘤:一例遗传起源不明的副神经节瘤独特病例

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

作者信息

Gibb Oliver, Lucas Jacob W, Deshpande Sujay, Edwards Daniel C

机构信息

Drexel University College of Medicine, Wyomissing, Pennsylvania, USA.

Center for Urologic Care of Berks County, Wyomissing, Pennsylvania, USA.

出版信息

Proc (Bayl Univ Med Cent). 2025 Jan 16;38(4):555-557. doi: 10.1080/08998280.2024.2448639. eCollection 2025.

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.

摘要

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内,副神经节瘤起源于腹膜后的交感神经链。尽管许多此类肿瘤临床上无明显症状,但经典表现为高肾上腺素能症状。我们报告一例患者,其腹膜后巨大肿块被发现是临床上无症状的副神经节瘤。该肿瘤不寻常的大小和表现以及未确定的基因起源为这种罕见肿瘤提供了独特的视角。

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