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皮肤恶性树突状细胞肉瘤:2 例罕见肉瘤亚型并文献复习

Malignant Dendritic Cell Sarcomas in the Skin: 2 Cases of Rare Sarcoma Subtypes With Literature Review.

机构信息

Department of Dermatology, Columbia University Medical Center, New York, NY.

Department of Dermatology, Virginia Commonwealth University Health System, Richmond, VA.

出版信息

Am J Dermatopathol. 2024 Nov 1;46(11):e106-e111. doi: 10.1097/DAD.0000000000002797. Epub 2024 Jul 12.

Abstract

Interdigitating dendritic cell sarcoma is a rare, aggressive hematological malignancy primarily originating in lymph nodes, with only 10 reported cases presenting in the skin (primary cutaneous interdigitating dendritic cell sarcoma). Past presentations showed erythematous nodules on the proximal extremities, back, or face. Morphologically, these neoplasms are similar to melanomas and other dendritic cell (DC) tumors, making their diagnosis difficult. Here, we present 1 case of primary cutaneous interdigitating dendritic cell sarcomas and another 1 of malignant indeterminate dendritic cell tumor (indeterminate DC sarcoma). The first case is an 83-year-old man who presented with recent ulceration and bleeding of an asymptomatic, slow growing lesion on his right thigh with biopsy revealing a large, well-circumscribed polypoid spindle cell tumor in the dermis with atypical cells with vesicular nuclei in a lymphoplasmacytic background and immunohistochemistry positivity for CD45, CD68, S100, and Cyclin D1. The second case is a 74-year-old man who presented with a progressively darkening and enlarging abdominal skin lesion with biopsy revealing a diffuse infiltrate of atypical poorly differentiated pleomorphic nuclear cells and immunohistochemistry positivity for S100, CD1a, CD56, CD43, cyclin D1, CD31, CD4, and BRAF V600E. Our findings contribute to expand the reported literature on primary cutaneous DC sarcomas.

摘要

交错突状细胞肉瘤是一种罕见的侵袭性血液恶性肿瘤,主要起源于淋巴结,仅有 10 例报告发生于皮肤(原发性皮肤交错突状细胞肉瘤)。既往表现为四肢近端、背部或面部出现红斑结节。从形态上看,这些肿瘤与黑色素瘤和其他树突状细胞(DC)肿瘤相似,导致诊断困难。在此,我们报告了 1 例原发性皮肤交错突状细胞肉瘤和 1 例恶性未定型树突状细胞瘤(未定型 DC 肉瘤)。第 1 例为 83 岁男性,右大腿有一无症状、生长缓慢的病变,最近出现溃疡和出血,活检显示真皮内有一个大的、边界清楚的息肉样梭形细胞肿瘤,伴有非典型细胞,在淋巴浆细胞背景中有泡状核,免疫组织化学 CD45、CD68、S100 和 Cyclin D1 阳性。第 2 例为 74 岁男性,腹部皮肤病变逐渐变黑和增大,活检显示弥漫性浸润性不典型分化差的多形性核细胞,免疫组织化学 S100、CD1a、CD56、CD43、Cyclin D1、CD31、CD4 和 BRAF V600E 阳性。我们的发现有助于扩大原发性皮肤 DC 肉瘤的报告文献。

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