| Literature DB >> 27195706 |
Madhu Rajeshwari1, Vaishali Suri1, Kavneet Kaur1, Ashish Suri2, Ajay Garg3, Mehar Chand Sharma1, Chitra Sarkar1.
Abstract
Intracranial lipomas are rare developmental lesions, predominantly occurring in the interhemispheric location. Osteochondrolipoma is an extremely rare variant of lipoma with osseous and chondroid differentiation. We present a case of interhemispheric osteochondrolipoma, in a 2.5-years-old male child which was detected antenatally, in association with corpus callosum agenesis. The lesion progressively increased in size with resulting compression of surrounding structures, and was subjected to microsurgical decompression. To the best of our knowledge, this is the first case of intracranial interhemispheric osteochondrolipoma in the existing medical literature. Peculiarities of this case and the diagnostic and surgical challenges are discussed.Entities:
Keywords: chondrolipoma; corpus callosum agenesis; intracranial lipoma; osteochondrolipoma; osteolipoma
Mesh:
Year: 2016 PMID: 27195706 DOI: 10.1111/neup.12294
Source DB: PubMed Journal: Neuropathology ISSN: 0919-6544 Impact factor: 1.906