Nodal Merkel Cell Carcinoma With Neuroblastoma Differentiation: A Case Report and Review of the Literature

IF 0.1 Q4 PATHOLOGY AJSP: reviews & reports Pub Date : 2021-01-25 DOI:10.1097/PCR.0000000000000412
L. Mahapatra, M. Mansour, D. Chatterjee, R. Fields, H. Maluf, L. Dehner
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Abstract

Abstract We report a case of a neuroendocrine carcinoma of the inguinal lymph node without a known identified primary site, which demonstrated the morphologic and immunophenotypic features of a Merkel cell carcinoma with neuroblastic differentiation. The neoplasm had a predominant high-grade neuroendocrine component with small cell features and a contiguous area with lobular foci of neuroblastic rosettes and fibrillary neuropil. Merkel cell carcinoma can occasionally demonstrate aberrant differentiation to other epithelial and nonepithelial cell lines, and this case is only the fourth in the available literature with neuroblastic differentiation. It is necessary to exclude a primary site of origin, but a few cases of primary neuroendocrine tumor of the lymph node have been described, with the inguinal region as the most common site of occurrence.
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结性默克尔细胞癌伴神经母细胞瘤分化:1例报告及文献复习
摘要我们报告一例腹股沟淋巴结神经内分泌癌,原发部位未知,表现出神经母细胞分化的默克尔细胞癌的形态学和免疫表型特征。肿瘤以高级别神经内分泌成分为主,具有小细胞特征,相邻区域有神经母细胞玫瑰花和原纤维神经瘤的小叶灶。默克尔细胞癌偶尔会表现出向其他上皮和非上皮细胞系的异常分化,该病例仅是现有文献中第四个神经母细胞分化的病例。排除原发部位是必要的,但有一些原发性淋巴结神经内分泌肿瘤的病例被描述,腹股沟区域是最常见的发生部位。
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