Journal of neuro-oncology · 2005
Primary meningeal pheochromocytoma: case report.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Mercuri Sandro, Gazzeri Roberto, Galarza Marcelo, Esposito Stefano, Giordano Marco
Аннотация
OBJECTIVE AND IMPORTANCE: Intracranial pheochromocytomas are extremely rare tumors. Reported cases include metastatic tumors without known cases of primary pheochromocytomas.
CLINICAL PRESENTATION: A female patient with a history of a surgically treated adrenal pheochromocytoma presented 23 years later with headache, nausea and blood hypertension. A head CT scan demonstrated a right temporoparietal meningeal heterogeneous lesion with a surrounding hyperdense ring. No other lesions were disclosed.
INTERVENTION: The lesion developed in the inner and outer surface of the dura without brain infiltration and it was totally resected. The patient is free of disease 6 years after brain surgery.
CONCLUSION: To our knowledge this is the first reported case of a primary meningeal pheochromocytoma.
CLINICAL PRESENTATION: A female patient with a history of a surgically treated adrenal pheochromocytoma presented 23 years later with headache, nausea and blood hypertension. A head CT scan demonstrated a right temporoparietal meningeal heterogeneous lesion with a surrounding hyperdense ring. No other lesions were disclosed.
INTERVENTION: The lesion developed in the inner and outer surface of the dura without brain infiltration and it was totally resected. The patient is free of disease 6 years after brain surgery.
CONCLUSION: To our knowledge this is the first reported case of a primary meningeal pheochromocytoma.