恶性软骨腔瘤:两例肉瘤性间充质成分的报告

IF 1.6 Q3 DERMATOLOGY
Dermatopathology Pub Date : 2019-06-26 DOI:10.1159/000495610
C. Nel, Dawn van der Byl, W. Grayson
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引用次数: 7

摘要

恶性软骨样汗管瘤(MCS;恶性混合瘤)是一种罕见的肿瘤,通常发生在四肢和躯干。我们报告了2例独特的MCS病例,一例发生在78岁男性的头皮上,另一例发生于72岁女性的躯干上。这两种肿瘤都含有恶性上皮和恶性间充质成分。后者在第一例中表现为脂肪肉瘤。第二个肿瘤的恶性成分包括梭形细胞鳞状细胞癌(SCC)和骨肉瘤。起源于先前存在的良性软骨样汗管瘤在这两种肿瘤中都很明显。然而,迄今为止,在MCS的背景下,异源恶性间充质成分的存在尚未报道,而梭形细胞SCC成分异常罕见。本文介绍的2例病例突出了MCS的扩展形态谱,导致MCS和皮肤癌肉瘤之间的边界模糊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Malignant Chondroid Syringoma: A Report of Two Cases with a Sarcomatous Mesenchymal Component
Malignant chondroid syringoma (MCS; malignant mixed tumour) is a rare neoplasm typically arising on the extremities and trunk. We are report 2 unique cases of MCS, one occurring on the scalp of a 78-year-old man and the other on the trunk of a 72-year-old woman. Both tumours harboured malignant epithelial and malignant mesenchymal components. The latter was represented by liposarcoma in the first case. The malignant components of the second tumour comprised spindle cell squamous cell carcinoma (SCC) and osteosarcoma. Origin from a pre-existing benign chondroid syringoma was clearly evident in both neoplasms. The presence of heterologous malignant mesenchymal components, however, is hitherto unreported in the context of MCS, while a spindle cell SCC component is exceptionally rare. The 2 cases presented herein highlight an expanded morphological spectrum of MCS, with resultant blurring of the boundaries between MCS and cutaneous carcinosarcoma.
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来源期刊
Dermatopathology
Dermatopathology DERMATOLOGY-
自引率
5.30%
发文量
39
审稿时长
11 weeks
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