首页> 外文期刊>Journal of Medical Case Reports >Clinical presentation and endoscopic features of primary gastric Burkitt lymphoma in childhood, presenting as a protein-losing enteropathy: a case report
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Clinical presentation and endoscopic features of primary gastric Burkitt lymphoma in childhood, presenting as a protein-losing enteropathy: a case report

机译:儿童原发性胃伯基特淋巴瘤的临床表现和内镜特征,表现为蛋白丢失性肠病:1例

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Introduction Burkitt lymphoma and B cell lymphomas in childhood may arise in many atypical locations, which on rare occasions can include gastric mucosa. A case of primary gastric Burkitt lymphoma is described in a child presenting as a protein-losing enteropathy, including the direct monitoring of the disease response by sequential endoscopic biopsy and molecular analysis. Case presentation We report a 9-year-old boy who presented with gross oedema, ascites and respiratory distress caused by a protein-losing enteropathy. Initial imaging investigations were non-diagnostic but gastroduodenal endoscopy revealed massive involvement of the gastric mucosa with a primary Burkitt lymphoma. His subsequent clinical progress and disease response were monitored directly by endoscopy and he remains in clinical remission 4 years after initial diagnosis. Conclusions This is the first case report of primary Burkitt lymphoma presenting as a protein-losing enteropathy. The clinical course and progress of the patient were monitored by sequential endoscopic biopsy, histology and molecular analysis by fluorescence in situ hybridisation.
机译:引言儿童时期的伯基特淋巴瘤和B细胞淋巴瘤可能出现在许多非典型部位,在极少数情况下可能包括胃粘膜。一例儿童原发性胃伯基特淋巴瘤病例描述为一种蛋白质丢失性肠病,包括通过连续内镜活检和分子分析直接监测疾病反应。病例介绍我们报告了一个9岁男孩,他因蛋白丢失性肠病而出现严重水肿,腹水和呼吸窘迫。最初的影像学检查无诊断意义,但十二指肠胃镜检查显示胃黏膜大量累及原发性伯基特淋巴瘤。他的后续临床进展和疾病反应通过内窥镜检查直接监测,并且在最初诊断后4年仍处于临床缓解状态。结论这是第一例原发性伯基特淋巴瘤表现为蛋白丢失性肠病的病例报告。通过连续的内窥镜活检,组织学和分子分析通过荧光原位杂交监测患者的临床病程和进展。

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