MNGI-08. A RARE CASE OF INFANTILE PAPILLARY RHABDOID MENINGIOMA
نویسندگان
چکیده
منابع مشابه
Meningioma with rhabdoid, papillary and clear cell features: case report and review of association of rare meningioma variants
Meningiomas are common central nervous system tumors with a wide range of morphological variants, assigned World Health Organization (WHO) Grades I - III. We report an extremely rare rhabdoid, papillary and clear cell meningioma (WHO Grade III) in a 29-year-old female, who presented with diplopia and headache over a few days, 2 years ago. Magnetic resonance imaging showed a well-circumscribed, ...
متن کاملPapillary meningioma: a rare but distinct variant of malignant meningioma
BACKGROUND Papillary meningiomas are rare meningeal tumors and are associated with aggressive clinical behavior as compared with other meningiomas. Because of their rare occurrence, they may pose a diagnostic dilemma to the unwary pathologist. We report a case of papillary meningioma in a 16-year-old boy. CASE PRESENTATION A 16-year-old boy presented with complaints of headache, progressively...
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Rhabdoid meningioma is a rare aggressive variant of meningioma, regarded as WHO grade III type. Histologically and cytologically, it is distinctive type having abundant eosinophilic cytoplasm, cytoplasmic inclusion with eccentrically placed vesicular nuclei and prominent nucleoli. High recurrence rate and poor outcome are important features. Here we are presenting a rare case of rhabdoid mening...
متن کاملRhabdoid Meningioma of Brain - A Rare Aggressive Tumor
Rhabdoid meningioma is a rare aggressive variant of meningioma, regarded as WHO Grade III type. Histologically and cytologically, it is distinctive type having abundant eosinophilic cytoplasm, cytoplasmic inclusion with eccentrically placed vesicular nuclei and prominent nucleoli. High recurrence rate and poor outcome are important features. Here, we are presenting a rare case of rhabdoid menin...
متن کاملPediatric Rhabdoid Meningioma
A 3-year-old boy, with a recent history of seizures, was admitted to the Neurosurgery Unit of the Meyer Children’s Hospital. He was the full-term result of a normal pregnancy. His weight was 17 kilograms and his cranial circumference was 50 cm. There were no neurological focal deficits or signs and symptoms of cranial hypertension. Neurocutaneous stigmata were absent. Computed tomography (CT) s...
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ژورنال
عنوان ژورنال: Neuro-Oncology
سال: 2018
ISSN: 1522-8517,1523-5866
DOI: 10.1093/neuonc/noy148.624