一名儿科患者同时患有髓母细胞瘤和 Chiari I 型畸形

IF 0.3 Q3 MEDICINE, GENERAL & INTERNAL Cukurova Medical Journal Pub Date : 2023-09-30 DOI:10.17826/cumj.1315981
İlknur SÜRÜCÜ KARA, Tayfun ÇAKIR
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引用次数: 0

摘要

髓母细胞瘤和Chiari畸形(1型)同时发生在儿科患者中是非常罕见的。10岁的女孩。她最初主诉恶心、腹痛和呕吐。她轻微头痛了三天。进行计算机断层扫描。有与既往疾病相关的后遗症,左侧小脑扁桃体延伸至枕骨大孔水平,第三脑室轻度突出。颅脑成像采用磁共振成像。右小脑水平区见一实性肿块,大小约60 mm,磁共振示小脑扁桃体疝(11 mm),心室扩张。组织学表现为典型的成神经管细胞瘤。两种疾病的共存可能发生在同一患者身上。磁共振成像显示颅椎交界处可以单独使用。因为MRG是首选的诊断方法。
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Pediatrik bir hastada eş zamanlı medulloblastoma ve Chiari Tip-I deformitesi
Concurrence of medulloblastoma and Chiari deformity (type-1) in a pediatric patient is extremely rarely seen. 10 years old girl. She had first complained of nausea, abdominal pain, and vomiting. She had a mild headache for three days. Computed tomography was taken. There were sequelae related to her previous illness and noticed the appearance of the left cerebellar tonsils down to the foramen magnum level and mild prominence in the third ventricle. Cranial imaging was performed with magnetic resonance imaging. There was a lesion as a solid mass, about 60 mm sized in the level right cerebellar, a cerebellar tonsil hernia (11 mm), and ventricular dilatation in magnetic resonance imaging. Histologically, the lesion was a classic type of medulloblastoma. The coexistence of two diseases may occur in the same patient. Magnetic resonance imaging, which indicates the craniovertebral junction can be used singly.Because MRG is the first method to be selected for diagnosis.
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来源期刊
Cukurova Medical Journal
Cukurova Medical Journal MEDICINE, GENERAL & INTERNAL-
自引率
0.00%
发文量
159
审稿时长
12 weeks
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