胃肠道表现作为神经疾病的初始表现
Pravarshini Datla1, Sowmya Gopalan1, Preetam Arthur1
1Internal Medicine, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Cureus
|November 3, 2025
概括
肌性缩症是一种遗传性疾病,可以出现不寻常的胃肠道症状,如慢性腹. 这一案例凸显了考虑肌性衰变的重要性,即使肌肉衰弱不是主要症状.
科学领域:
- 遗传学和罕见疾病.
- 胃肠病学 胃肠病学
- 神经肌肉疾病 神经肌肉疾病
背景情况:
- 肌性缩症 (MD) 是一种多系统性疾病,通常表现为渐进性的肌肉衰弱.
- 胃肠道 (GI) 问题是MD不常见的初始症状,往往导致误诊.
- 早期白内障和糖尿病可能与MD有关.
研究的目的:
- 报告一个罕见的肌性缩病例.
- 强调慢性腹作为MD的初始表现.
- 为了突出诊断的挑战,当胃肠道症状之前肌肉骨的迹象.
主要方法:
- 案例报告的呈现方式.
- 审查患者的病史,包括糖尿病和早期白内障.
- 慢性腹的临床和诊断评估.
主要成果:
- 一个年轻的成年男性呈现慢性腹作为第一个明显的症状.
- 在最初的胃肠道表现时,肌肉骨表现不存在.
- 该患者有糖尿病病史和早期白内障.
结论:
- 慢性腹可能是肌性衰竭的非典型初始表现.
- 在患有无法解释的胃肠道症状和相关并发症的患者中,考虑MD至关重要.
- 早期识别可以防止肌性营养不良的诊断延迟.
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