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罕见的巨大腹膜后黑色素性神经鞘瘤:一例报告并文献复习

Rare giant retroperitoneal melanotic schwannoma: a case report and literature review.

作者信息

Chen Pan, Cheng Junfeng, Zhang Lin

机构信息

Department of Gynecology, Jinhua Municipal Central Hospital, Jinhua, Zhejiang, China.

Department of Hepatopancreatobiliary Surgery, Jinhua Municipal Central Hospital, Jinhua, Zhejiang, China.

出版信息

Front Oncol. 2024 Aug 29;14:1448112. doi: 10.3389/fonc.2024.1448112. eCollection 2024.

DOI:10.3389/fonc.2024.1448112
PMID:39267844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11390348/
Abstract

BACKGROUND

Melanotic schwannoma (MS), a rare variant of peripheral nerve sheath tumor, is especially infrequent when originating from the peritoneum. Its definitive diagnosis relies on postoperative histopathological examination and immunohistochemical analysis, while preoperative diagnosis is difficult.

CASE PRESENTATION

In the present study, we reported a rare case of giant MS in the retroperitoneum, which was previously misdiagnosed before surgery. However, intraoperative exploration revealed it was retroperitoneal tumor. The tumor had invaded the abdominal aorta and bilateral common illiac artery walls. A surgical resection was subsequently executed, and postoperative histopathological examination confirmed it as a MS.

CONCLUSION

The incidence of peritoneal MS is extremely rare, and surgical resection remains the preferred treatment modality. Given the absence of established guidelines for postoperative adjuvant therapy, long-term follow-up becomes imperative to accumulate valuable clinical expertise.

摘要

背景

黑色素性神经鞘瘤(MS)是周围神经鞘瘤的一种罕见变异型,起源于腹膜时尤为少见。其明确诊断依赖于术后组织病理学检查和免疫组化分析,而术前诊断困难。

病例报告

在本研究中,我们报告了一例罕见的腹膜后巨大MS病例,该病例术前曾被误诊。然而,术中探查发现它是腹膜后肿瘤。肿瘤侵犯了腹主动脉和双侧髂总动脉壁。随后进行了手术切除,术后组织病理学检查证实为MS。

结论

腹膜MS的发病率极低,手术切除仍然是首选的治疗方式。鉴于缺乏术后辅助治疗的既定指南,长期随访势在必行,以积累宝贵的临床经验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/099528e9807e/fonc-14-1448112-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/be27f234504e/fonc-14-1448112-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/d2df4f67f9bf/fonc-14-1448112-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/099528e9807e/fonc-14-1448112-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/be27f234504e/fonc-14-1448112-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/d2df4f67f9bf/fonc-14-1448112-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c40b/11390348/099528e9807e/fonc-14-1448112-g003.jpg

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J Neurosurg Spine. 2023 Oct 20;40(1):28-37. doi: 10.3171/2023.8.SPINE23427. Print 2024 Jan 1.
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Free Neuropathol. 2022 Aug 26;3:21. doi: 10.17879/freeneuropathology-2022-3864. eCollection 2022 Jan.
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Checkpoint inhibitors and radiotherapy in refractory malignant melanocytic schwannoma with Carney complex: first evidence of efficacy.
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The 2020 WHO Classification of Tumors of Soft Tissue: Selected Changes and New Entities.《2020 年世卫组织软组织肿瘤分类:精选变更和新实体》。
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Pathology of Melanotic Schwannoma.黑色素性雪旺细胞瘤的病理学。
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