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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.

DOI:10.1016/j.eucr.2019.100926
PMID:31297325
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6597528/
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/6597528/334489f08514/egi10PDSS97JHW.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/1e72169a75ad/egi10GB88TQDLJ.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/435b069d3168/egi10S6L2TKL5V.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/334489f08514/egi10PDSS97JHW.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/1e72169a75ad/egi10GB88TQDLJ.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/435b069d3168/egi10S6L2TKL5V.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be2d/6597528/334489f08514/egi10PDSS97JHW.jpg

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引用本文的文献

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Adrenal schwannoma: why should endocrinologists be aware of this uncommon tumour?

本文引用的文献

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Juxta-adrenal schwannoma presenting as a giant adrenal tumor: A case report and a literature review.表现为巨大肾上腺肿瘤的肾上腺旁神经鞘瘤:一例报告及文献复习
Int J Surg Case Rep. 2018;53:132-136. doi: 10.1016/j.ijscr.2018.10.017. Epub 2018 Oct 15.
2
MR imaging features of benign retroperitoneal paragangliomas and schwannomas.良性腹膜后副神经节瘤和神经鞘瘤的磁共振成像特征
BMC Neurol. 2018 Jan 4;18(1):1. doi: 10.1186/s12883-017-0998-8.
3
A rare adrenal incidentaloma: adrenal schwannoma.一例罕见的肾上腺偶发瘤:肾上腺神经鞘瘤。
肾上腺神经鞘瘤:为什么内分泌学家应该了解这种不常见的肿瘤?
Endocrine. 2022 Mar;75(3):684-697. doi: 10.1007/s12020-022-02997-x. Epub 2022 Feb 12.
4
Benign adrenal and suprarenal retroperitoneal schwannomas can mimic aggressive adrenal malignancies: case report and review of the literature.良性肾上腺及肾上腺后腹膜神经鞘瘤可酷似侵袭性肾上腺恶性肿瘤:病例报告及文献复习
Intractable Rare Dis Res. 2020 Aug;9(3):156-162. doi: 10.5582/irdr.2020.01027.
5
Schwannoma Misdiagnosed as Adrenal Adenoma: A Case Report and Review of the Literature.误诊为肾上腺腺瘤的神经鞘瘤:一例报告及文献复习
Case Rep Endocrinol. 2020 Jan 30;2020:8020761. doi: 10.1155/2020/8020761. eCollection 2020.
Case Rep Gastroenterol. 2013 Oct 5;7(3):420-7. doi: 10.1159/000355871. eCollection 2013.
4
Special problems encountering surgical management of large retroperitoneal schwannomas.巨大腹膜后神经鞘瘤手术治疗中遇到的特殊问题。
World J Surg Oncol. 2008 Oct 3;6:107. doi: 10.1186/1477-7819-6-107.
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Schwannoma in the peridiaphragm.膈肌周围的神经鞘瘤。
Gen Thorac Cardiovasc Surg. 2008 Sep;56(9):453-5. doi: 10.1007/s11748-008-0269-0. Epub 2008 Sep 13.