Division of Pathology, Kanagawa Children's Medical Center, Yokohama 232-8555, Japan.
Hum Pathol. 2011 Oct;42(10):1568-72. doi: 10.1016/j.humpath.2010.12.022. Epub 2011 Apr 15.
We report a case of malignant steroidogenic tumor arising from a sacrococcygeal teratoma in a 5-year-old girl. A congenital gluteal mass and a 7-month history of precocious puberty had been noted, and a large estrogen-producing tumor in the sacrococcygeal area was found. After a biopsy, chemotherapy and tumor resection were performed, and no recurrence has been observed. The biopsy specimen showed small clusters of atypical round cells adjacent to a mature teratoma. They had large round nuclei with prominent nucleoli and abundant eosinophilic cytoplasms and were positive for vimentin, steroidogenic factor-1, inhibin α, and melan-A. Increased mitoses, vascular invasion, and necrosis were noted. The tumor was diagnosed as sacrococcygeal mature teratoma, with malignant steroidogenic tumor as somatic malignant transformation. Although several kinds of somatic malignant transformation of sacrococcygeal teratoma have been reported, to the best of our knowledge, this is the first case of malignant steroidogenic tumor arising from sacrococcygeal teratoma.
我们报告了一例 5 岁女孩骶尾部畸胎瘤起源的恶性类固醇细胞瘤。患者曾有先天性臀部长肿块和 7 个月的性早熟病史,在骶尾部发现一个产生大量雌激素的肿瘤。行活检、化疗和肿瘤切除后,未见复发。活检标本显示成熟畸胎瘤旁有小簇异型圆形细胞。这些细胞的圆形细胞核大,核仁明显,胞质嗜酸性丰富,免疫组化显示波形蛋白、类固醇生成因子-1、抑制素 α 和黑素-A 阳性。可见核分裂象增多、血管浸润和坏死。肿瘤诊断为骶尾部成熟畸胎瘤,伴恶性类固醇细胞瘤的体骼恶性转化。虽然已有多种骶尾部畸胎瘤的体骼恶性转化的报道,但据我们所知,这是首例骶尾部畸胎瘤起源的恶性类固醇细胞瘤。