Dieckgraefe Brian K, Korzenik Joshua R, Husain Asif, Dieruf Lisa
Washington University School of Medicine 660 S Euclid Ave, Campus Box 8124, St Louis, MO 63110, USA.
Eur J Pediatr. 2002 Oct;161 Suppl 1:S88-92. doi: 10.1007/s00431-002-1011-z. Epub 2002 Aug 13.
Glycogen storage disease (GSD)-1b has been associated with neutropenia and abnormalities of neutrophil function. Many individuals with GSD-1b manifest chronic gastrointestinal inflammation. Our study was performed to precisely establish the type, frequency, and spectrum of gastrointestinal disease in patients with GSD-lb. We established a medical database of 36 individuals affected with GSD-1b, utilizing patients at our center, disease registries, and direct contacts with North American referral centers specializing in genetic disorders. Records were reviewed, focusing on documentation of gastrointestinal involvement. Gastrointestinal symptoms or manifestations were present in approximately 75% of the patients, including chronic abdominal pain and diarrhea, perianal fistula or abscess, and oral aphthous ulceration. Of patients identified, 28% had documented inflammatory bowel disease (IBD) and an additional 22% of patients had symptoms highly suggestive of IBD, but had not undergone comprehensive diagnostic evaluation. Gastrointestinal involvement was found to be indistinguishable from idiopathic Crohn disease (CD) by detailed review of clinical, radiologic, endoscopic and histopathologic findings. Many patients had significant improvement or resolution of gastrointestinal disease in response to G-CSF treatment. The expression of CD in patients with GSD-1b may be delayed or prevented by G-CSF treatment.
a strong association exists between glycogen storage disease type 1b and inflammatory bowel disease. A high index of suspicion for Crohn disease should be applied in evaluating patients with glycogen storage disease type 1b and intestinal symptoms. These results provide further support for the hypothesis that some forms of inflammatory bowel disease may result from impaired mucosal innate immunity. Additional investigations into the intestinal disease in glycogen storage disease type 1b may be directly relevant to the etiology and treatment of idiopathic Crohn disease.
糖原贮积病(GSD)-1b与中性粒细胞减少及中性粒细胞功能异常有关。许多GSD-1b患者表现出慢性胃肠道炎症。我们开展这项研究是为了准确确定GSD-1b患者胃肠道疾病的类型、频率和范围。我们利用本中心的患者、疾病登记处以及与北美遗传性疾病转诊中心的直接联系,建立了一个包含36名GSD-1b患者的医学数据库。对记录进行了审查,重点是胃肠道受累情况的记录。约75%的患者存在胃肠道症状或表现,包括慢性腹痛、腹泻、肛周瘘管或脓肿以及口腔阿弗他溃疡。在确诊的患者中,28%有炎症性肠病(IBD)的记录,另外22%的患者有高度提示IBD的症状,但未接受全面的诊断评估。通过对临床、放射学、内镜和组织病理学检查结果的详细审查发现,胃肠道受累与特发性克罗恩病(CD)难以区分。许多患者在接受粒细胞集落刺激因子(G-CSF)治疗后,胃肠道疾病有显著改善或缓解。G-CSF治疗可能会延迟或预防GSD-1b患者CD的发生。
1b型糖原贮积病与炎症性肠病之间存在密切关联。在评估1b型糖原贮积病且有肠道症状的患者时,应高度怀疑克罗恩病。这些结果为某些形式的炎症性肠病可能由黏膜固有免疫受损引起这一假说提供了进一步支持。对1b型糖原贮积病肠道疾病的进一步研究可能与特发性克罗恩病的病因和治疗直接相关。