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伪装成肾上腺皮质肿瘤的神经鞘瘤:一例报告并文献复习

Schwannoma masquerading as adrenocortical tumor: A case report and review of literature.

作者信息

Shabana Waleed, Raslan Wasim, Hassan Said, Al-Tartir Tareq

机构信息

Johns Hopkins Aramco Healthcare-Urology Department, Saudi Arabia.

Faculty of Medicine-Zagazig University-urology Department, Egypt.

出版信息

Urol Case Rep. 2019 May 30;26:100926. doi: 10.1016/j.eucr.2019.100926. eCollection 2019 Sep.

Abstract

Schwannomas arises from retroperitoneal space are rare tumors. Adrenal Schwannomas are often misdiagnosed due to deficient of distinctive radiological findings. We report a case of adrenal schwannoma presented with vague abdominal pain. Initially, the patient was diagnosed as adrenocortical tumor that was treated with robotic adrenalectomy. Histopathological and immuno-histochemical examination revealed schwannoma. We will report the case and review the literature regarding this rare tumor.

摘要

起源于腹膜后间隙的神经鞘瘤是罕见肿瘤。肾上腺神经鞘瘤常因缺乏独特的影像学表现而被误诊。我们报告一例以腹部隐痛为表现的肾上腺神经鞘瘤病例。最初,该患者被诊断为肾上腺皮质肿瘤并接受了机器人辅助肾上腺切除术。组织病理学和免疫组织化学检查显示为神经鞘瘤。我们将报告该病例并复习有关这种罕见肿瘤的文献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/1e72169a75ad/egi10GB88TQDLJ.jpg

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