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Primary Intraocular Malignant Rhabdoid Tumor Mimicking Retinoblastoma in a Child
Author(s) -
Nirupama Kasturi,
Pratik Gera,
Gayatri Panicker,
Ajax Jossy,
Vidhyalakshmi Rangarajan,
Srinivas Bheemanathi Hanuman
Publication year - 2020
Publication title -
ocular oncology and pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.444
H-Index - 10
eISSN - 2296-4681
pISSN - 2296-4657
DOI - 10.1159/000510206
Subject(s) - retinoblastoma , medicine , pathology , differential diagnosis , soft tissue , central nervous system , retina , biology , neuroscience , biochemistry , gene
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.

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