Khyber Medical University, KMU-IMS, Kohat, Pakistan.
Mercy Saint Vincent Medical Center, Toledo, OH, USA.
Medicine (Baltimore). 2022 Oct 21;101(42):e31350. doi: 10.1097/MD.0000000000031350.
Celiac disease (CD) is autoimmune enteropathy affecting the proximal small intestinal mucosa. It is caused by insensitivity to gluten, a protein predominantly presented in wheat. CD is classically associated with gastrointestinal symptoms. The non-classic clinical presentation of CD can present with other organ involvement. Non-human leukocyte antigens genes are associated with atypical forms.
We reported a case of 30-year-old female who presented with progressive pallor, amenorrhea, and unexplained weight loss with generalized body weakness. Her body mass index was 20. The patient was having no other systemic manifestations.
This paper reports a case of a female patient having CD without its typical features. Her laboratory evaluation revealed microcytic anemia. Anti-TTg IgA and Anti-TTG IgG antibodies were raised, ferritin and folate were low, and there was mild hyperbilirubinemia. However, follicle-stimulating hormone, luteinizing hormone, and serum estradiol levels were normal. She was diagnosed with a case of anemia resulting from malabsorption caused by CD.
A management plan was devised based on a strict gluten-free diet. The patient received supplements containing folates, iron, calcium, zinc, and vitamins A, D, E, B6, and B12.
After 3 months of treatment with strict gluten-free diet patient showed remarkable improvement. Her hemoglobin level raised with weight gain. Her normal menstrual cycle was restored with complete resolution of symptoms at 1 year follow-up.
The pathogenesis of the atypical CD is multifactorial, but impaired uptake of micronutrients from the duodenum is the most likely cause, even if other common features of classical forms, such as bloating and diarrhea, are absent. Lack of awareness about atypical forms may lead to under-diagnoses of the disease. The physicians should consider the atypical presentations of CD to avoid the under-diagnoses of this multisystem disorder.
乳糜泻(CD)是一种影响近端小肠黏膜的自身免疫性肠病。它是由对主要存在于小麦中的蛋白质——麸质的不敏感引起的。CD 通常与胃肠道症状相关。CD 的非典型临床表现可出现其他器官受累。非人类白细胞抗原基因与非典型形式相关。
我们报告了一例 30 岁女性患者,她表现为进行性苍白、闭经和不明原因的体重减轻伴全身无力。她的体重指数为 20。患者没有其他全身表现。
本文报告了一例无典型特征的女性 CD 患者。她的实验室评估显示小细胞性贫血。抗 TTG IgA 和抗 TTG IgG 抗体升高,铁蛋白和叶酸降低,轻度高胆红素血症。然而,卵泡刺激素、黄体生成素和血清雌二醇水平正常。她被诊断为由于 CD 引起的吸收不良导致的贫血。
根据严格的无麸质饮食制定了治疗计划。患者接受了含有叶酸、铁、钙、锌和维生素 A、D、E、B6 和 B12 的补充剂。
经过 3 个月的严格无麸质饮食治疗,患者病情显著改善。她的血红蛋白水平升高,体重增加。她的正常月经周期恢复,在 1 年的随访中症状完全缓解。
非典型 CD 的发病机制是多因素的,但十二指肠对微量营养素的吸收不良是最可能的原因,即使缺乏经典形式的其他常见特征,如腹胀和腹泻。对非典型表现缺乏认识可能导致该疾病的漏诊。医生应考虑 CD 的非典型表现,以避免这种多系统疾病的漏诊。