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具有罕见肛门部位的神经鞘瘤。

Schwannoma with an uncommon anal location.

作者信息

Pan Jiyong, Jing Huirong, Tian Xiaofeng, Fan Zhe

机构信息

Department of General Surgery, The Third People's Hospital of Dalian, Dalian, Liaoning 116000, P.R. China.

Department of General Surgery, The Second Hospital of Dalian Medical University, Dalian, Liaoning 116000, P.R. China.

出版信息

Oncol Lett. 2014 Nov;8(5):1945-1946. doi: 10.3892/ol.2014.2459. Epub 2014 Aug 19.

DOI:10.3892/ol.2014.2459
PMID:25295076
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4186604/
Abstract

Schwannomas are slow-growing mesenchymal neoplasms that arise from Schwann cells with low malignant potential. These uncommon neoplasms are nerve sheath tumors that arise at almost any anatomical site. The majority of schwannomas are benign, and few are malignant. The current study presents the rare case of an anal schwannoma that was successfully treated by surgery; there are few such cases previously reported in the literature. The patient was admitted to hospital following the identification of a mass incidentally. The tumor was so large that it compressed the tissue around it, although no symptoms were caused. The pre-operative clinical diagnosis was inconclusive in this case, and a final diagnosis was established based on radiographic and histopathological examination. The current study aimed to provide a possible differential diagnosis for such anally-located masses.

摘要

施万细胞瘤是一种生长缓慢的间叶性肿瘤,起源于恶性潜能较低的施万细胞。这些不常见的肿瘤是神经鞘瘤,几乎可发生于任何解剖部位。大多数施万细胞瘤是良性的,恶性的很少。本研究报告了一例罕见的经手术成功治疗的肛门施万细胞瘤病例;此前文献报道的此类病例很少。患者因偶然发现肿块入院。肿瘤很大,虽未引起症状,但压迫了周围组织。该病例术前临床诊断不明确,最终诊断基于影像学和组织病理学检查。本研究旨在为这种位于肛门的肿块提供可能的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/4186604/6048cc9a9086/OL-08-05-1945-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/4186604/5a1a3e948ebc/OL-08-05-1945-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/4186604/6048cc9a9086/OL-08-05-1945-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/4186604/5a1a3e948ebc/OL-08-05-1945-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8946/4186604/6048cc9a9086/OL-08-05-1945-g01.jpg

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Lingual schwannoma: case report and review of the literature.舌部神经鞘瘤:病例报告及文献复习。
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The management of retroperitoneal giant schwannomas in AIDS patients: A case report.艾滋病患者腹膜后巨大神经鞘瘤的治疗:一例报告。
Oncol Lett. 2013 Apr;5(4):1430-1432. doi: 10.3892/ol.2013.1191. Epub 2013 Feb 13.
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Pelvic schwannoma in the right parametrium.右侧附件区盆腔神经鞘瘤。
BMC Res Notes. 2016 Jun 13;9:304. doi: 10.1186/s13104-016-2108-1.
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Giant abdominoperineal malignant schwannoma: an unusual presentation and surgical challenge.巨大型腹会阴恶性神经鞘瘤:一种不寻常的表现及手术挑战。
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Operative treatment of Schwannoma, the primary sacral tumor--case presentation.原发性骶骨肿瘤神经鞘瘤的手术治疗——病例报告
Pol Orthop Traumatol. 2012 May 30;77:10-6.
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Giant presacral schwannoma presenting with constipation: a case report.以便秘为表现的巨大骶前神经鞘瘤:一例报告
J Med Case Rep. 2012 Sep 10;6:285. doi: 10.1186/1752-1947-6-285.
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Schwannoma of the conus medullaris: a rare case.圆锥神经鞘瘤:1例罕见病例
Chin J Cancer. 2011 Dec;30(12):867-70. doi: 10.5732/cjc.011.10213. Epub 2011 Nov 15.
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Common bile duct schwannoma: a case report and review of literature.胆总管神经鞘瘤:一例病例报告及文献复习
World J Gastroenterol. 2007 Feb 28;13(8):1275-8. doi: 10.3748/wjg.v13.i8.1275.
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Imaging features of retroperitoneal and pelvic schwannomas.腹膜后及盆腔神经鞘瘤的影像学特征。
Clin Radiol. 2005 Aug;60(8):886-93. doi: 10.1016/j.crad.2005.01.016.
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Retroperitoneal giant schwannomas: report on two cases and review of the literature.腹膜后巨大神经鞘瘤:两例报告并文献复习
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