Eosinophilic gastroenteritis in a 14-year-old patient with Noonan syndrome with a PTPN11 variation: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Nobuhiko Koga, Shuichi Yatsuga, Kei Kubota, Toshikazu Niimi, Takahito Inoue, Shinichiro Nagamitsu
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Abstract

Background: Noonan syndrome has a wide range of symptoms due to dysregulation of the RAS/MAPK pathway with several gene variations, including the PTPN11 gene. There are currently no case reports of Noonan syndrome with eosinophilic gastroenteritis.

Case: A 14-year-old Japanese girl was clinically diagnosed with Noonan syndrome. She had intermittent abdominal pain and vomiting from 10 years old. The patient was diagnosed with eosinophilic gastroenteritis on the basis of the pathological finding of multiple foci with > 20 eosinophils/high power field in the mucosal lamina propria of the colon by endoscopy at 12 years old. Vomiting and abdominal pain are currently being controlled by antihistamines and leukotriene antagonist therapy. Genetic testing showed the missense variation p.Ala72Gly in the PTPN11 gene.

Discussion: The pathogenesis of eosinophilic gastroenteritis is similar to that of other allergic inflammatory diseases, such as bronchial asthma. The cause of eosinophilic gastroenteritis is multifactorial, including genetic and environmental factors. The PTPN11 gene variations are suggested to promote eosinophilic disorders by leading to the activation of the RAS/MAPK pathway. This activation subsequently results in the production of interleukin-5, which plays a crucial role in the pathogenesis of eosinophilic gastroenteritis. The relationship between eosinophilic gastroenteritis and the PTPN11 gene has not yet been reported.

Conclusion: We herein present the first known case of eosinophilic gastroenteritis in Noonan syndrome with a variation in the PTPN11 gene. The relationship between Noonan syndrome and eosinophilic gastroenteritis remains unknown; therefore, additional case reports of Noonan syndrome with eosinophilic gastroenteritis are required to elucidate this potential relationship.

14岁努南综合征伴PTPN11变异患者嗜酸性胃肠炎1例报告。
背景:Noonan综合征由于RAS/MAPK通路失调,包括PTPN11基因在内的多种基因变异而具有广泛的症状。目前尚无努南综合征合并嗜酸性胃肠炎的病例报告。病例:一名14岁的日本女孩被临床诊断为努南综合征。她从10岁起就有间歇性腹痛和呕吐。患者12岁时,经内镜检查发现结肠粘膜固有层多灶灶伴bbbb20嗜酸性粒细胞/高倍场,诊断为嗜酸性胃肠炎。呕吐和腹痛目前由抗组胺药和白三烯拮抗剂治疗控制。基因检测显示PTPN11基因存在p.Ala72Gly错义变异。讨论:嗜酸性胃肠炎的发病机制与其他过敏性炎症性疾病如支气管哮喘相似。嗜酸性胃肠炎的病因是多因素的,包括遗传和环境因素。PTPN11基因变异可能通过激活RAS/MAPK通路来促进嗜酸性粒细胞疾病。这种激活随后导致白细胞介素-5的产生,白细胞介素-5在嗜酸性胃肠炎的发病机制中起关键作用。嗜酸性胃肠炎与PTPN11基因的关系尚未见报道。结论:我们在此报告第一例已知的Noonan综合征伴PTPN11基因变异的嗜酸性胃肠炎。Noonan综合征与嗜酸性胃肠炎的关系尚不清楚;因此,需要更多的努南综合征合并嗜酸性胃肠炎的病例报告来阐明这种潜在的关系。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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