原发性食管横纹肌肉瘤:小儿吞咽困难的罕见病因。

IF 0.6 Q4 GASTROENTEROLOGY & HEPATOLOGY
Case Reports in Gastrointestinal Medicine Pub Date : 2024-12-12 eCollection Date: 2024-01-01 DOI:10.1155/crgm/3648155
Maryam Ataollahi, Amirali Mashhadiagha, Fereshteh Karbasian, Reza Moshfeghinia, Javad Arabpour, Bita Geramizadeh
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引用次数: 0

摘要

背景:食管胚胎性横纹肌肉瘤(ERMS)是一种罕见的儿童癌症,在一个涉及吞咽困难和呕吐的病例中模仿贲门失弛缓症。由于潜在的并发症,诊断和化疗需要仔细监测。病例介绍:一名12岁女孩,无既往病史,表现为进行性吞咽困难和呕吐。初步诊断为贲门失弛缓症,但进一步检查发现一个大的纵隔肿块引起食管压迫。活检证实原发性食管ERMS伴转移。尽管化疗,她出现并发症,包括中性粒细胞减少性小肠结肠炎和后部可逆性脑病综合征(PRES)。不幸的是,她死于中性粒细胞减少性败血症。结论:在本病例研究中,除了文献中有限的信息外,我们还介绍了我们对该疾病的临床病程、治疗策略和预后的经验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary Esophageal Rhabdomyosarcoma: An Exceptionally Rare Cause of Pediatric Dysphagia.

Background: Esophageal embryonal rhabdomyosarcoma (ERMS), a rare pediatric cancer, mimicked achalasia in a case involving dysphagia and vomiting. Diagnosis and chemotherapy necessitate careful monitoring due to potential complications. Case presentation: A 12-year-old girl with no prior medical history presented with progressive dysphagia and vomiting. Initial diagnosis suggested achalasia, but further evaluation revealed a large mediastinal mass causing esophageal compression. Biopsies confirmed primary ERMS of the esophagus with metastases. Despite chemotherapy, she developed complications, including neutropenic enterocolitis and posterior reversible encephalopathy syndrome (PRES). Unfortunately, she succumbed to neutropenic sepsis. Conclusion: In this case study, we presented our experience regarding the clinical course of this disease, treatment strategy, and prognosis, in addition to the limited previous information in the literature.

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来源期刊
Case Reports in Gastrointestinal Medicine
Case Reports in Gastrointestinal Medicine GASTROENTEROLOGY & HEPATOLOGY-
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