| Literature DB >> 26875176 |
Aanchal Kakkar1, Saphalta Baghmar2, Ajay Garg3, Vaishali Suri1, Vinod Raina2, Chitra Sarkar1, Mehar Chand Sharma4.
Abstract
Rhabdoid meningioma is a rare meningioma variant, classified as WHO grade III. Although this tumor is known for its aggressive behavior and poor prognosis, extracranial metastasis is rare. We report the rare case of a 31-year-old patient with rhabdoid meningioma which recurred several times despite gross total resection, radiation therapy, and gamma knife radiosurgery, and the last recurrence was associated with metastases to lungs, lymph node and bone. The patient showed no response to paclitaxel-carboplatin, or vincristine-cyclophosphamide-adriamycin chemotherapy, and succumbed to the disease. Metastases from rhabdoid meningioma prove to be a diagnostic challenge, and treatment for metastatic meningiomas is not optimized, thus necessitating documentation and interdisciplinary consensus on management protocols.Entities:
Keywords: Immunohistochemistry; Lymph node; Meningioma; Metastases; Rhabdoid
Mesh:
Year: 2016 PMID: 26875176 DOI: 10.1007/s10014-016-0250-z
Source DB: PubMed Journal: Brain Tumor Pathol ISSN: 1433-7398 Impact factor: 3.298