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神经母细胞瘤患儿消化道相关副肿瘤综合征的罕见原因:三例报告

Uncommon reasons of the digestive tract-related paraneoplastic syndromes in children with neuroblastic tumors: three case reports.

作者信息

Czkwianianc Elżbieta, Zalewska-Szewczyk Beata, Kobos Józef, Socha-Banasiak Anna, Janczar Szymon, Prymus-Kasińska Sylwia, Kazanek-Zasada Joanna, Młynarski Wojciech

机构信息

Gastroenterology, Allergology and Pediatric Department, Polish Mother's Memorial Hospital Research Institute, Lodz, Poland.

Department of Pediatrics, Oncology, Hematology and Diabetology, Medical University of Lodz, Lodz, Poland.

出版信息

Contemp Oncol (Pozn). 2018;22(1):42-46. doi: 10.5114/wo.2018.74393. Epub 2018 Apr 3.

Abstract

AIM OF THE STUDY

presentation of the uncommon paraneoplastic syndromes related to the gastrointestinal tract that may occur in children with neuroblastic tumors and their impact on the disease course.

MATERIAL AND METHODS

Retrospective analysis of three cases of patients mainly with digestive tract-related symptoms, who were originally admitted to the gastroenterology department from 2013 to 2016 and were finally diagnosed with neuroblastic tumors.

RESULTS

The clinical data analysis showed that the symptoms from gastrointestinal tract were dominant in analyzed subjects. The first case is a girl with weight loss, bloating and severe diarrhea, admitted to the hospital in a state of dehydration. The laboratory tests revealed severe hypokalemia. Finally, vasoactive intestinal peptide (VIP) secreting ganglioneuroblastoma was diagnosed and effective surgery was performed. The second case was also a girl who suffered from the incidents of watery diarrhea and flatulence. The tumor was detected by computerized tomography scan. The 3 stage of ganglioneuroblastoma was diagnosed. The patient required chemotherapy, radiotherapy and surgery treatment. The third child was a boy, hospitalized due to abdominal pain, constipation and weakness. During the diagnostic process, the 4 stage of neuroblastoma was recognized. The chemotherapy, surgery, radiotherapy and immunotherapy were applied.

CONCLUSIONS

In children with common abdominal symptoms as chronic flatulence, diarrhea or severe constipation of unknown etiology, the neuroblastic tumors should be considered.

摘要

研究目的

介绍神经母细胞瘤患儿可能出现的与胃肠道相关的罕见副肿瘤综合征及其对病程的影响。

材料与方法

回顾性分析2013年至2016年最初收治于消化内科、最终诊断为神经母细胞瘤的3例主要有消化道相关症状的患者。

结果

临床数据分析显示,在分析对象中胃肠道症状占主导。第一例是一名女孩,有体重减轻、腹胀和严重腹泻,因脱水入院。实验室检查显示严重低钾血症。最终诊断为分泌血管活性肠肽(VIP)的节细胞神经母细胞瘤,并进行了有效手术。第二例也是一名女孩,有腹泻和肠胃胀气发作。通过计算机断层扫描检测到肿瘤。诊断为节细胞神经母细胞瘤3期。患者需要化疗、放疗和手术治疗。第三个孩子是一名男孩,因腹痛、便秘和虚弱住院。在诊断过程中,确诊为神经母细胞瘤4期。应用了化疗、手术、放疗和免疫治疗。

结论

对于有慢性肠胃胀气、腹泻或病因不明的严重便秘等常见腹部症状的儿童,应考虑神经母细胞瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e23e/5910524/df96d544a137/WO-22-32265-g001.jpg

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