Atypical Presentation of a Pilocytic Astrocytoma at the Regional Hospital of Ségou in Mali country

S. A, Coulibaly, O. S, Beydari, B. H, K. A, D. M, T. B, T. H, Kané, M, K. M, Diallo, O, Dama, M, C. O, Touré, A, Mounkoro, M, Kanikomo, D
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Abstract

Introduction: Pilocytic astrocytoma is the most common cerebral glioma in pediatric age, preferentially located in the posterior cerebral fossa. Atypical presentations have rarely been described in the literature. Clinical Case: We report a case of pilocytic astrocytoma whose appearance on CT scan is unusual. It concerns a young boy of 9 years old, who presented convulsive seizures since the age of 6 years old, followed by general practitioners with irregular treatment based on gardenal. 2 months ago the seizures became more frequent and this prompted a specialist consultation with the neurologist, after a brain scan he referred the patient to us. The neurological examination was unremarkable today. Brain CT with contrast showed a right parietal lesion. It was a lesion with a double cystic and fleshy component associated with calcifications with heterogeneous enhancement which amputated the posterior horn of the lateral ventricle. The radiological appearance was in favor of a low-grade oligodendroglioma. The patient underwent surgery with complete macroscopic excision of the lesion. Histological examination revealed a pilocytic astrocytoma (grade I). Conclusion: The usual radiological appearance of pilocytic astrocytoma combines a cystic part and a highly contrasting mural nodule. It rarely presents in the form of a supratentorial lesion with calcifications. This form of presentation is rare and can lead to confusion with other gliomas. We can achieve healing for the patient with total excision.
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马里塞古地区医院出现的非典型嗜酸性星形细胞瘤
简介嗜酸性星形细胞瘤是小儿时期最常见的脑胶质瘤,好发于大脑后窝。非典型表现在文献中鲜有描述。临床病例:我们报告了一例在 CT 扫描中表现不寻常的朝粒细胞星形细胞瘤。病例涉及一名 9 岁的小男孩,他从 6 岁开始出现抽搐发作,全科医师对他进行了不规则的花园疗法治疗。2 个月前,他的癫痫发作变得更加频繁,这促使他向神经科专家求诊。今天的神经系统检查并无异常。造影剂脑 CT 显示右顶叶病变。该病变具有双重囊性和肉质成分,伴有钙化和异质强化,切断了侧脑室后角。放射学外观显示为低级别少突胶质细胞瘤。患者接受了手术,在大体上完全切除了病灶。组织学检查结果显示为朝粒细胞星形细胞瘤(I 级)。结论通常,朝珠细胞性星形细胞瘤的放射学表现为囊性部分和对比度较高的壁结节。它很少表现为伴有钙化的幕上病变。这种表现形式非常罕见,容易与其他胶质瘤混淆。我们可以通过全切除术使患者痊愈。
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