Janda J, Pecha V, Petrík F, Cízek F, Berková M, Stĕrba J, Gottschalk J
Department of Pathology, District Hospital, Ceský Krumlov, CSSR.
Arch Geschwulstforsch. 1988;58(5):333-40.
A case of 26-year old man, with a large primary retroperitoneal tumor which showed the pattern of embryonal carcinoma as well as yolk sac tumor, is reported. The disease ran an aggressive course and led to death within 8 months from the onset of clinical symptoms. Characteristic histological and ultrastructural patterns with Schiller-Duval bodies and adenocarcinomatous differentiation were accompanied by diffuse expression of alpha-fetoprotein and human chorionic gonadotropin expression in isolated cells, as well. The histogenesis of the tumor may be interpreted in terms of the reflection of the very early stages of the embryonal development rather than by the totipotent-neoplastic-germ-cell approach.
报告了一例26岁男性患者,患有巨大的原发性腹膜后肿瘤,其呈现出胚胎癌以及卵黄囊瘤的病理模式。该疾病进展迅速,自临床症状出现起8个月内导致患者死亡。具有席勒-杜瓦尔小体和腺癌分化的特征性组织学和超微结构模式,同时还伴有甲胎蛋白的弥漫性表达以及个别细胞中人绒毛膜促性腺激素的表达。肿瘤的组织发生可以从胚胎发育早期阶段的反映角度来解释,而非通过全能性肿瘤性生殖细胞途径来解释。