胃轻瘫、胸腺瘤和无症状肌无力:一种罕见的临床情况

IF 1.5 Q3 GASTROENTEROLOGY & HEPATOLOGY
C. Tamburella, S. Parisi, S. Lillo, G. Ferrantelli, P. Critelli, A. Viola, A. Platania, M. Santoro, A. Cacciola, A. Santacaterina, G. Ferini
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引用次数: 1

摘要

背景:副肿瘤性胃轻瘫是一种胃肠道综合征,很少在肿瘤诊断之前出现。为了提高对这种罕见临床实体的认识,我们报告了一例严重的胃轻瘫,后来被证明与胸腺瘤有关。病例报告:一名55岁的男子突然出现严重的腹部痉挛和腹胀,早期饱腹并伴有餐后恶心、反酸、打嗝和胀气。他瘦了大约20磅。体格检查和影像学检查显示胃胀、胃轻瘫,前纵隔有固体肿块。进行了根治性手术切除胸腺瘤,鉴于Mib-1的高价值,患者接受了术后胸部放射治疗。胸腺切除术后,诊断为副肿瘤性重症肌无力伴亚急性自主神经功能衰竭。结论:自身免疫性胃轻瘫应被视为胸腺瘤、重症肌无力和无机械性梗阻的胃排空延迟患者的潜在副肿瘤综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gastroparesis, Thymoma, and Asymptomatic Myasthenia: A Rare Clinical Scenario
Background: Paraneoplastic gastroparesis is a gastrointestinal syndrome that rarely precedes a tumor diagnosis. To increase awareness of this rare clinical entity, we present a case of severe gastroparesis, which was later proven to be associated with a thymoma. Case report: A 55-year old man had the sudden onset of severe abdominal cramps and abdominal distension, early satiety with postprandial nausea, acid regurgitation, belching, and flatulence. He lost about 20 pounds. The physical and imaging examination revealed stomach distension, gastroparesis, and the presence of a solid mass in the anterior mediastinum. Radical surgery was performed to remove the thymoma and, given the high value of Mib-1, the patient was submitted to postoperative chest radiation therapy. After thymectomy, a diagnosis of paraneoplastic myasthenia gravis with subacute autonomic failure was made. Conclusion: Autoimmune gastroparesis should be considered as a potential paraneoplastic syndrome in patients with thymoma, myasthenia gravis, and delayed gastric emptying in the absence of mechanical obstruction.
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来源期刊
Gastroenterology Insights
Gastroenterology Insights GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
2.80
自引率
3.40%
发文量
35
审稿时长
10 weeks
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