Kasturi Nirupama, Gera Pratik, Panicker Gayatri, Jossy Ajax, Rangarajan Vidhyalakshmi, Hanuman Srinivas Bheemanathi
Department of Ophthalmology, Jawaharlal Postgraduate Medical Education and Research, Puducherry, India.
Department of Pathology, Jawaharlal Postgraduate Medical Education and Research, Puducherry, India.
Ocul Oncol Pathol. 2020 Dec;6(6):438-441. doi: 10.1159/000510206. Epub 2020 Sep 23.
Primary rhabdoid tumors are highly malignant, rare tumors occurring in the renal, extrarenal soft tissue or central nervous system. They have non-specific radiological features and present with several histological components that create a problem in differential diagnosis with other embryonal tumors. We report a rare case of malignant rhabdoid tumor of the retina that presented with clinical features like those of retinoblastoma.
原发性横纹肌样瘤是一种高度恶性的罕见肿瘤,可发生于肾脏、肾外软组织或中枢神经系统。它们具有非特异性的放射学特征,并具有几种组织学成分,这给与其他胚胎性肿瘤的鉴别诊断带来了困难。我们报告了一例罕见的视网膜恶性横纹肌样瘤,其临床表现与视网膜母细胞瘤相似。