Ziemer M, Jäger I M, Dippel E
Klinik für Dermatologie, Venerologie und Allergologie, Universitätsklinikum Leipzig AöR, Philipp-Rosenthal-Str. 23, 04103, Leipzig, Deutschland.
Hautklinik, Klinikum der Stadt Ludwigshafen am Rhein gGmbH, Ludwigshafen, Deutschland.
Hautarzt. 2019 Sep;70(9):661-669. doi: 10.1007/s00105-019-04471-8.
Atypical fibroxanthoma (AFX) or undifferentiated pleomorphic sarcoma (UPS) is a rare malignant neoplastic disease of the skin. At the beginning of the 1960s AFX was described as an independent entity and superficial variant of malignant fibrous histiocytoma (MFH). Since then, many controversies on the classification have arisen mainly because in many cases dedifferentiated neoplasms from other origins were falsely diagnosed as AFX. A relevant deep expansion, the invasion of nerves and vessels or the presence of tumor necrosis are described as being typical for UPS; however, in the first-line they represent risk factors for recurrence. In view of the clinical and histological features it is meaningful to consider AFX and UPS as one disease. In recent years many studies on the molecular pathological background have attempted to make a better classification of the neoplasm, without being able to so far name a certain specific histopathological or molecular pathological characteristic. The AFX/UPS is still in essence a morphological and immunohistochemical diagnosis by exclusion.
非典型纤维黄色瘤(AFX)或未分化多形性肉瘤(UPS)是一种罕见的皮肤恶性肿瘤性疾病。20世纪60年代初,AFX被描述为一种独立的实体以及恶性纤维组织细胞瘤(MFH)的浅表变体。从那时起,关于分类出现了许多争议,主要是因为在许多情况下,其他起源的去分化肿瘤被错误地诊断为AFX。相关的深部扩展、神经和血管侵犯或肿瘤坏死的存在被描述为UPS的典型特征;然而,首先它们代表复发的危险因素。鉴于临床和组织学特征,将AFX和UPS视为一种疾病是有意义的。近年来,许多关于分子病理背景的研究试图对该肿瘤进行更好的分类,但迄今为止还无法确定某种特定的组织病理学或分子病理学特征。AFX/UPS本质上仍然是一种通过排除法进行的形态学和免疫组化诊断。