非典型纤维黄瘤
医学
未分化多形性肉瘤
肉瘤
病理
皮肤病科
软组织
隆突性皮肤纤维肉瘤
梅克尔细胞癌
软组织肉瘤
免疫组织化学
作者
Teo Soleymani,Sumaira Z. Aasi,Roberto A. Novoa,S. Tyler Hollmig
标识
DOI:10.1016/j.det.2019.02.001
摘要
Atypical fibroxanthoma and undifferentiated pleomorphic sarcoma , or pleomorphic dermal sarcoma, are rare malignant cutaneous neoplasms existing along a clinicopathologic spectrum. Although these tumors share many similarities, recognition of distinguishing characteristics may predict differences in clinical behavior and outcomes. Salient features defining atypical fibroxanthoma include superficial tumors with minimal high-risk histologic features. Deeper tumors with high-risk histologic features are often clinically aggressive and should be appropriately designated as pleomorphic dermal sarcoma. Surgery remains gold standard in management; tumor extirpation with complete margin control is critical. In the high-risk tumor cohort, comprehensive evaluation and multidisciplinary management is paramount for optimal outcomes.
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