Ooi A, Nakanishi I, Kojima M
Department of Pathology, School of Medicine, Kanazawa University, Japan.
Pathol Res Pract. 1992 Aug;188(6):770-4. doi: 10.1016/S0344-0338(11)80176-7.
This is the first case report of an unusual malignant tumor with components of malignant schwannoma, rhabdomyosarcoma, and melanoma, occurring in an adult. The tumor was observed in the left temple in a 35-year-old man without von Recklinghausen's disease. The possible derivation of this tumor from primitive neuroectodermal cells is discussed.
这是首例关于一名成年人发生的具有恶性神经鞘瘤、横纹肌肉瘤和黑色素瘤成分的罕见恶性肿瘤的病例报告。该肿瘤在一名35岁无冯雷克林霍增氏病的男性左侧颞部被观察到。本文讨论了该肿瘤可能起源于原始神经外胚层细胞的情况。