Garber J E, Burke E M, Lavally B L, Billett A L, Sallan S E, Scott R M, Kupsky W, Li F P
Clinical Studies Section, National Cancer Institute, Bethesda, Maryland.
Cancer. 1990 Dec 15;66(12):2658-60. doi: 10.1002/1097-0142(19901215)66:12<2658::aid-cncr2820661232>3.0.co;2-c.
Choroid plexus neoplasms are rare epithelial tumors of the central nervous system. A carcinoma of the choroid plexus occurred in a child from a family with the breast cancer-sarcoma syndrome (Li-Fraumeni or SBLA syndrome), an inherited condition characterized by the development of diverse neoplasms (sarcoma, breast cancer, brain tumors, leukemia, adrenal cortical carcinoma, and others). Choroid plexus carcinomas were identified in two kindreds previously reported with the syndrome. The literature contains reports of choroid plexus neoplasms occurring in families and in individuals with multiple primary tumors. Choroid plexus neoplasm may be a manifestation of the inherited proclivity to tumor development in the breast cancer-sarcoma syndrome.
脉络丛肿瘤是中枢神经系统罕见的上皮性肿瘤。一名患有乳腺癌-肉瘤综合征(李-弗劳梅尼综合征或SBLA综合征)的儿童发生了脉络丛癌,该综合征是一种遗传性疾病,其特征是发生多种肿瘤(肉瘤、乳腺癌、脑肿瘤、白血病、肾上腺皮质癌等)。先前报道的两个患有该综合征的家族中发现了脉络丛癌。文献中有关于脉络丛肿瘤发生在有多个原发性肿瘤的家族和个体中的报道。脉络丛肿瘤可能是乳腺癌-肉瘤综合征中遗传性肿瘤发生倾向的一种表现。