Buehler Darya, Weisman Paul
Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, 600 Highland Avenue, L5/184 CSC, Madison, WI 53792, USA.
Department of Pathology and Laboratory Medicine, University of Wisconsin School of Medicine and Public Health, 600 Highland Avenue, B1779 WIMR, Madison, WI 53792, USA.
Clin Lab Med. 2017 Sep;37(3):647-671. doi: 10.1016/j.cll.2017.06.005.
The mesenchymal tumors discussed herein represent a heterogeneous group of neoplasms with distinctive morphologic, immunophenotypic, and molecular genetic features. These uncommon tumors often arise in the dermis and subcutis and can pose a major diagnostic challenge to dermatopathologists because they closely mimic melanoma, carcinoma, fibrous histiocytoma, schwannoma, or granulomatous inflammation. This article reviews the clinical presentation, histopathology, differential diagnosis, and diagnostic pitfalls of epithelioid sarcoma, clear cell sarcoma, perivascular epithelioid cell tumor, ossifying fibromyxoid tumor, pleomorphic hyalinizing angiectatic tumor, and hemosiderotic fibrolipomatous tumor. Associated molecular genetic findings are also briefly reviewed with an emphasis on their diagnostic usefulness.
本文所讨论的间充质肿瘤是一组异质性肿瘤,具有独特的形态学、免疫表型和分子遗传学特征。这些不常见的肿瘤常发生于真皮和皮下组织,对皮肤病理学家来说是一个重大的诊断挑战,因为它们与黑色素瘤、癌、纤维组织细胞瘤、神经鞘瘤或肉芽肿性炎症极为相似。本文综述了上皮样肉瘤、透明细胞肉瘤、血管周上皮样细胞肿瘤、骨化性纤维黏液样肿瘤、多形性透明变性血管扩张性肿瘤和含铁血黄素性纤维脂肪瘤的临床表现、组织病理学、鉴别诊断及诊断陷阱。还简要回顾了相关的分子遗传学发现,重点强调其诊断价值。