Desmoplastic Infantile Astrocytoma in a 47-day Old Male Infant with Four-year Follow-up: A Rare Case Report and Literature Review

S. Taghipour zahir, M. Mortaz, K. Rahmani, Farzan Safi Dahaj
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Abstract

Desmoplastic infantile astrocytoma/ganglioglioma (DIA/DIG) is a rare mixed neuronalglial solid cystic brain tumor found in infantile cerebral hemispheres. The main presentation of the tumor is the rapidly enlarging of the head circumference with hydrocephalus and seizure. DIA is classified as a WHO Grade 1 brain tumor but, due to the rarity of the tumor, few studies are available on tumor survival and prognosis. Herein, we report a 47-day-old male infant diagnosed with DIA and the four-year follow-up.
1例47天大的男婴结缔组织增生星形细胞瘤,随访4年:一例罕见病例报告及文献复习
结缔组织成形性婴儿星形细胞瘤/神经节胶质瘤(DIA/DIG)是一种罕见的混合神经节胶质实性囊性脑肿瘤,发现于婴儿大脑半球。主要表现为头围迅速增大,伴脑积水和癫痫发作。DIA被WHO列为1级脑肿瘤,但由于肿瘤的罕见性,关于肿瘤生存和预后的研究很少。在此,我们报告了一名47天大的男婴被诊断为DIA并进行了四年的随访。
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