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1型神经纤维瘤病突变在恶性黑色素瘤十二指肠病变中被检测到的尸检病例:一例报告

An Autopsy Case of Neurofibromatosis Type 1 Mutation Detected in a Duodenal Lesion of Malignant Melanoma: A Case Report.

作者信息

Seki Mai, Saitou Emi, Saito Shintaro, Araki Takeshi, Shinohara Yoichiro, Fujihira Kazuyoshi, Oyama Tetsunari, Yokoo Hideaki

机构信息

Diagnostic Pathology, Gunma University Graduate School of Medicine, Maebashi, JPN.

Dermatology, Gunma University Graduate School of Medicine, Maebashi, JPN.

出版信息

Cureus. 2025 Aug 25;17(8):e90933. doi: 10.7759/cureus.90933. eCollection 2025 Aug.

Abstract

We report an autopsy case of duodenal malignant melanoma (MM) in a patient with neurofibromatosis type 1 (NF1). The patient had an anamnesis of choroidal MM, and the duodenal lesion was initially suspected to be a metastasis from the choroidal tumor. At autopsy, the duodenum was occupied by a tumor composed of large atypical cells on histopathological examination. Immunohistochemically, the nuclei of large atypical cells were positive for Melan A, HMB-45, and SOX-10, confirming the diagnosis of MM. Next-generation sequencing (NGS) of the duodenal tumor sample identified an NF1 mutation, with no other gene mutations clearly associated with malignant transformation.

摘要

我们报告了1例1型神经纤维瘤病(NF1)患者发生十二指肠恶性黑色素瘤(MM)的尸检病例。该患者有脉络膜MM病史,十二指肠病变最初被怀疑是脉络膜肿瘤转移所致。尸检时,组织病理学检查显示十二指肠被一个由大的非典型细胞组成的肿瘤占据。免疫组化显示,大的非典型细胞核Melan A、HMB-45和SOX-10呈阳性,确诊为MM。对十二指肠肿瘤样本进行的二代测序(NGS)发现了一个NF1突变,未发现其他与恶性转化明显相关的基因突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f4/12458915/1c3efb5e7f62/cureus-0017-00000090933-i01.jpg

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