Guérard M J, Ferenczy A, Arguelles M A
Ultrastruct Pathol. 1982 Oct-Dec;3(4):347-58. doi: 10.3109/01913128209018557.
The clinical and light and electron microscopic findings of a moderately differentiated, virilizing, Sertoli-Leydig cell tumor (SLT) with pleomorphic rhabdomyosarcoma of the ovary are presented. The tumor recapitulates the primitive embryonal testis and rhabdomyogenesis, respectively. The natural history, including pathogenesis, of this peculiar and rare tumor is discussed in the light of the pertinent literature on SLT and ovarian rhabdomyosarcoma. It seems that when rhabdomyosarcoma is a significant or predominant component of SLT, as occurred in this case, the prognosis is poor and is that of rhabdomyosarcoma in general.
本文报告了一例伴有卵巢多形性横纹肌肉瘤的中度分化、具有男性化特征的支持-间质细胞瘤(SLT)的临床、光镜及电镜检查结果。该肿瘤分别再现了原始胚胎睾丸和横纹肌发生过程。结合关于支持-间质细胞瘤和卵巢横纹肌肉瘤的相关文献,对这种特殊罕见肿瘤的自然病史,包括发病机制进行了讨论。似乎当横纹肌肉瘤是支持-间质细胞瘤的主要或显著成分时,如本病例所示,预后较差,与一般横纹肌肉瘤的预后相同。