Argani P, Athanasian E
Department of Pathology, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.
Arch Pathol Lab Med. 1997 Sep;121(9):992-5.
We report a rare malignant endovascular papillary angioendothelioma (Dabska tumor) arising within the deep periosteal soft tissue of the ulna of an 8-year-old girl. To our knowledge, this is the first report of a Dabska tumor of deep soft tissue that did not extend down from the dermis. This Dabska tumor appears to be a focal change within a larger, well-defined, cavernous hemangioma of deep muscle. We suggest that this represents secondary neoplastic progression of an existing benign lesion, a common phenomenon among vascular tumors. A review of the family of "hobnailed" endothelial cell lesions to which Dabska tumor belongs is presented.
我们报告了一例罕见的恶性血管内乳头状血管内皮瘤(达布斯卡瘤),发生于一名8岁女孩尺骨深骨膜软组织内。据我们所知,这是第一例深软组织达布斯卡瘤未从真皮向下延伸的报道。该达布斯卡瘤似乎是深部肌肉内一个较大的、边界清晰的海绵状血管瘤内的局灶性改变。我们认为这代表了现有良性病变的继发性肿瘤进展,这在血管肿瘤中是一种常见现象。本文还对达布斯卡瘤所属的“鞋钉样”内皮细胞病变家族进行了综述。