Fouad Khalil Elouadghiri, Ghanam Ayad, Hamami Amal, Haloui Anass, Babakhouya Abdeladim, Rkain Maria
Department of Pediatrics, Faculty of Medicine and Pharmacy, Mohamed First University, Oujda, MAR.
Department of Pediatrics, Mohammed VI University Hospital Center, Oujda, MAR.
Cureus. 2025 Aug 9;17(8):e89681. doi: 10.7759/cureus.89681. eCollection 2025 Aug.
We report the case of a nine-year-old boy who presented with severe pancytopenia and respiratory distress. His medical history was notable for pica, chronic epigastric pain, pallor, and intermittent vomiting. Initial laboratory investigations revealed profound anemia (Hemoglobin (Hb) 2 g/dL), neutropenia, thrombocytopenia, and significant deficiencies in vitamin B12 and vitamin D. Serologic testing was positive for anti-transglutaminase IgA antibodies, and duodenal biopsies confirmed celiac disease (CD) (Marsh stage 3a), along with gastritis. Management consisted of a strict gluten-free diet, vitamin supplementation, and eradication therapy. Over the following year, the patient demonstrated marked clinical improvement, with normalization of hematologic parameters, nutritional status, and growth. This case highlights the importance of considering CD in the differential diagnosis of unexplained pancytopenia in pediatric patients, even in the absence of overt gastrointestinal symptoms.
我们报告了一名9岁男孩的病例,他出现了严重的全血细胞减少和呼吸窘迫。他的病史以异食癖、慢性上腹部疼痛、面色苍白和间歇性呕吐为特征。初始实验室检查显示严重贫血(血红蛋白(Hb)2 g/dL)、中性粒细胞减少、血小板减少以及维生素B12和维生素D显著缺乏。血清学检测抗转谷氨酰胺酶IgA抗体呈阳性,十二指肠活检证实为乳糜泻(CD)(马什3a期),同时伴有胃炎。治疗包括严格的无麸质饮食、维生素补充和根除治疗。在接下来的一年里,患者临床症状明显改善,血液学参数、营养状况和生长均恢复正常。该病例强调了在儿科患者不明原因全血细胞减少的鉴别诊断中考虑CD的重要性,即使没有明显的胃肠道症状。