ATYPICAL INTERPRETATION OF MEDULLOBLASTOMA

R. Panda, Pratosh Paul, S. Mishra, S. Mishra
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Abstract

Introduction: Medulloblastoma is a midline posterior fossa mass that typically develops from the vermis in children. It shows up on a CT scan as a hyperdense, homogeneously enhancing mass and is linked to the clinical profile of posterior fossa syndrome. Although this distinct clinical-radiological pattern is regarded as "typical," medulloblastomas frequently do not follow the normal clinico-radiological pattern. Methods: To identify the abnormal clinical-radiological features, 28 patients were retrospectively analyzed and 12 cases were prospectively studied. Only 21 of the 40 patients showed the typical radiological feature of a hyperdense homogeneously enhancing mass, while the other four had hypodense nonenhancing masses, 12 had cystic alterations, and five had calcifications in their tumors. Three patients arrived with tumors in the cerebellopontine angle cistern, which is a rather rare position. Results: Patients who underwent follow-up for a minimum of 6 months and a maximum of 1 year returned with metastases in very odd places. There were 2 patients who had a cervical intramedullary metastasis, and there were 4 occurrences of metastases in the frontal and subfrontal area. One year following final surgery and ventriculoperitoneal shunting, abdominal metastases and ascites occurred in 3 individuals. But after surgery, each of these 3 patients had had a complete course of craniospinal irradiation. Conclusion: There were other cases that had atypical clinical, radiological, and metastatic patterns.
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髓母细胞瘤的不典型解释
髓母细胞瘤是一种典型的儿童后窝中线肿块,起源于蚓部。CT扫描显示为高密度均匀增强肿块,与后窝综合征的临床表现有关。虽然这种独特的临床放射学模式被认为是“典型的”,但髓母细胞瘤经常不遵循正常的临床放射学模式。方法:对28例患者进行回顾性分析,并对12例患者进行前瞻性分析。40例患者中只有21例表现出典型的高密度均匀增强肿块,而其他4例为低密度非增强肿块,12例有囊性改变,5例肿瘤有钙化。3例患者到达时肿瘤位于桥小脑角池,这是一个相当罕见的位置。结果:随访时间最少6个月,最多1年的患者复发时转移部位非常奇怪。宫颈髓内转移2例,额叶及额下转移4例。在最后一次手术和脑室-腹膜分流后一年,3例发生腹腔转移和腹水。但在手术后,这3名患者都进行了完整的颅脊髓照射。结论:还有其他病例具有不典型的临床,放射学和转移模式。
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