Kraemer B B, Silva E G, Sneige N
Am J Surg Pathol. 1984 Mar;8(3):231-6.
An 8-year-old child with nevoid basal-cell carcinoma syndrome who developed abdominal pain underwent exploratory laparotomy. Both ovaries were enlarged and replaced by fibroblastic proliferations having cellular foci with high mitotic indices (greater than 4 mitoses/10 high-power fields) diagnostic of fibrosarcoma. Two years following salpingo-oophorectomy, a metastasis was excised from one adnexa. Further recurrence or distant metastasis was not evident after 6 more years of follow-up. The association of fibrosarcoma of the ovary in a patient with nevoid basal-cell carcinoma further expands the multifarious nature of this syndrome.
一名患有痣样基底细胞癌综合征的8岁儿童出现腹痛,接受了剖腹探查术。双侧卵巢均增大,被纤维母细胞增生所取代,这些增生具有细胞灶,有高有丝分裂指数(大于4个有丝分裂/10个高倍视野),诊断为纤维肉瘤。输卵管卵巢切除术后两年,从一个附件切除了一处转移灶。经过6年多的随访,未见进一步复发或远处转移。痣样基底细胞癌患者发生卵巢纤维肉瘤,进一步扩展了该综合征的多样性。