Format

Send to

Choose Destination
Asian J Neurosurg. 2019 Jan-Mar;14(1):253-255. doi: 10.4103/ajns.AJNS_176_17.

Phosphaturic Mesenchymal Tumors Involving Skull Bones: Report of Two Rare Cases.

Author information

1
Department of Histopathology, Bombay Hospital and Medical Research Centre, Mumbai, Maharashtra, India.

Abstract

Phosphaturic mesenchymal tumor (PMT) is a rare tumor causing oncogenic osteomalacia (OO). Most such tumors occur in soft tissue and bones of extremities and appendicular skeleton. Intracranial location and involvement of temporal-occipital bone is extremely rare. We report two unusual cases: The first was intracranial, involving the temporal bone, while the other was a skull base tumor arising from the occipital-temporal bone. Both of them presented with paraneoplastic syndrome of OO, resembled a meningioma radiologically, and underwent gross total resection of tumor. Histologically, both of them were diagnosed as PMT, mixed connective tissue variant.

KEYWORDS:

Fibroblast growth factor-23; intracranial; oncogenic osteomalacia; phosphaturic mesenchymal tumor; temporal–occipital bone

Supplemental Content

Full text links

Icon for Medknow Publications and Media Pvt Ltd Icon for PubMed Central
Loading ...
Support Center