Singh Avninder, Jairajpuri Zeeba, Gupta Vikas, Sharma Shruti, Chand Karam
Institute of Pathology, ICMR, Safdarjung Hospital Campus, New Delhi - 110 029, India.
Indian J Pathol Microbiol. 2008 Jul-Sep;51(3):389-91. doi: 10.4103/0377-4929.42521.
Atypical teratoid /rhabdoid tumor (AT/RT) of the central nervous system is a rare but highly aggressive neoplasm that usually affects young children and infants and follows a rapidly fatal course. We report a case of AT/RT in a 3-month-old male infant who also had coincidental unilateral congenital cataract even though there was no associated congenital infectious disease.
中枢神经系统非典型畸胎样/横纹肌样瘤(AT/RT)是一种罕见但侵袭性很强的肿瘤,通常影响幼儿和婴儿,病程进展迅速,预后凶险。我们报告一例3个月大男婴患AT/RT的病例,该男婴同时伴有单侧先天性白内障,尽管并无相关先天性传染病。