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作 者:卢璐 刘嫦钦[1] 吴维 曾美英 沙梦玲 陈春球 刘占举[1] 孙晓敏[1] Lu Lu;Liu Changqin;Wu Wei;Zeng Meiying;Sha Mengling;Chen Chunqiu;Liu Zhanju;Sun Xiaomin(Department of Gastroenterology,the Shanghai Tenth People′s Hospital,Tongji University School of Medicine,Shanghai 200072,China;Department of Gastroenterology,Longhua Hospital,Shanghai University of Traditional Chinese Medicine,Shanghai 200032,China;Department of Radiology and Imaging,the Shanghai Tenth People′s Hospital,Tongji University School of Medicine,Shanghai 200072,China;Department of Pathology,the Shanghai Tenth People′s Hospital,Tongji University School of Medicine,Shanghai 200072,China;Diagnostic and Treatment for Refractory Diseases of Abdomen Surgery,the Shanghai Tenth People′s Hospital,Tongji University School of Medicine,Shanghai 200072,China)
机构地区:[1]同济大学附属上海第十人民医院消化科,200072 [2]上海中医药大学附属龙华医院脾胃病科,200032 [3]同济大学附属上海第十人民医院放射影像科,200072 [4]同济大学附属上海第十人民医院病理科,200072 [5]同济大学附属上海第十人民医院腹部疑难外科,200072
出 处:《中华炎性肠病杂志(中英文)》2023年第2期201-203,共3页Chinese Journal of Inflammatory Bowel Diseases
摘 要:糖原累积症(GSD)-Ib型是常染色体隐性遗传性疾病, 常伴发炎症性肠病。现报道1例GSD-Ib合并克罗恩病样肠炎的病例, 希望诊疗过程有助于提高临床医师对此罕见病的认识。Glycogen storage disease(GSD)-type Ib is an autosomal recessive disease,often accompanied by inflammatory bowel disease.A case of GSD-Ib combined with Crohn′s disease-like enterocolitis is reported.The diagnosis and treatment of this patient is helpful to improve the understanding of this rare disease.
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