Meningiomas in children are rare. They represent only 1% to 3% of all intracranial tumors. It was a case report of a childhood girl meningioma, which is from the rare tumor and presenting by seizures, evolving in an apyretic context. She had no notion of irradiation or particular personal history apart from wearing glasses since the age of 5 years. She weighed 70 kg (BMI = 31). Biological examinations were normal. The brain scan showed a left frontal extra-axial tumor process measuring 76 × 60 × 55 mm. Tumor resection was performed. Macroscopically, the surgical specimen was found to be 8 firm, lobulated, yellowish-white fragments measuring 14 × 11 × 2 cm and weighing 150 g in total. The histological examination showed a proliferation of meningothelial cells, with a tendency to stratify and to roll up on each other in an onion bulb shape, without excess of mitoses and without cortical infiltration, evoking a meningioma. Meningioma in children remains a rare tumor. In our case, seizures were the only revealing signs of this disease. Cerebral computed tomography oriented the diagnosis. Anatomopathological examination was essential for confirmation.

Cervical Pott's disease is a rare localization of spinal tuberculosis. The diagnosis of this affection is most often late which exposes to serious neurological complications. The diagnosis is often delayed by bundles of clinical and biological arguments and aided by the CT scan of the cervical spine. We report a new case of C3-C4 cervical tuberculosis in an immunocompetent woman. The diagnosis was confirmed by the presence of Koch's bacillus (BK) in the gastric fluid after tubing. The treatment is based on the twelve-month anti-tuberculosis drug and a spinal stabilization by cervical osteosynthesis.