血管肉瘤
医学
异型性
恶性肿瘤
头皮
病态的
病理
血管肉瘤
病变
核异型性
介绍(产科)
皮肤病科
放射科
免疫组织化学
作者
Giovanni Paolino,Viviana Lora,Carlo Cota,Chiara Panetta,Luca Muscardin,Pietro Donati
出处
期刊:American Journal of Dermatopathology
[Ovid Technologies (Wolters Kluwer)]
日期:2016-07-14
卷期号:38 (9): 690-694
被引量:7
标识
DOI:10.1097/dad.0000000000000677
摘要
Angiosarcoma (AS) is a rare malignant vascular tumor, which affects mainly elderly patients. After the diagnosis, the mean overall survival of patients is 30 months. The variable presentation of the malignancy, the benign appearance of the cutaneous lesions, and the minimal histological changes in early lesions can sometimes delay the correct diagnosis. The authors report a case of an 80-year-old white male patient, with a painless and ecchymotic lesion of the scalp, which histologically showed minimal pathological atypia, conclusive for a diagnosis of AS with minimal histological changes. The authors discuss the main and most emblematic cases of AS initially misdiagnosed for other cutaneous diseases reported in the literature, noting that in some cases, also the histology can be treacherous and a trap for the dermatopathologist. The recent findings on MYC, FLT4 and KDR amplification, and the relative therapeutic perspectives are also discussed. Finally, the authors draw up some pathological cornerstones, which could improve the diagnosis, above all in early lesions with minimal atypia.
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