儿童多结节性Desmoplastic髓母细胞瘤:一种罕见的放射生理学检查

Song-ping Zheng, S. Richard, Yiyun Fu, Yan Ju, C. You
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引用次数: 0

摘要

髓母细胞瘤的结节性结缔组织增生性变异体虽然很常见,但其放射学特征与儿童下、下蚓的其他病变相似。我们报告一例罕见的纤维间质增殖性髓母细胞瘤的影像学表现。病例介绍:1岁零9个月大的男性,表现为行走不稳,呕吐持续2周。他在生病之前显然走路很好。呕吐通常发生在早晨,并伴有头痛。影像学显示小脑虫区异常肿块,双侧脑室及第三脑室明显增大,提示脑积水。手术成功,显微镜和免疫组化检查证实为结缔组织增塑性髓母细胞瘤。结论:成神经管细胞瘤虽不罕见,但在影像学诊断上存在很大问题。我们希望我们的影像学发现能更清楚地阐明该肿瘤的放射学特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multi-nodular Desmoplastic Medulloblastoma in a Child: A Rare Radiological Physiognomy
Introduction: Nodular desmoplastic variant of medulloblastoma although very common, can present with very challenging radiological feature that mimics others lesions in the inferior and lower vermis in children. We present a case of rare radiological appearance of desmoplastic medullobastoma. Case Presentation: A one year and nine months old male presented with unstable walking and projectile vomiting of two weeks’ duration. He was apparently walking well prior this illness. The vomiting was usually in the morning and associated with headaches. Radiological imaging revealed very unusual masses in the cerebellum vermin region with obvious bilateral ventricular enlargement as well as the third ventricle, indicating hydrocephalus. Surgery was successful carried out and microscopic as well as immunohistochemistry confirmed desmoplastic medullobastoma. Conclusion: Desmoplastic medulloblastoma although not very rare can be very problematic in terms of radiological diagnosis. We are of the option that our imaging finding will throw more light on the radiological features of this tumor.
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