Ma Hui-Ru, Mu Shu-Chi, Yang Yao-Hsu, Chen Chung-Min, Chiang Bor-Luen
Department of Pediatrics, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
J Formos Med Assoc. 2003 Mar;102(3):189-92.
Chronic granulomatous disease (CGD) is an inherited phagocytic disorder caused by defective oxidative burst activity of neutrophils and monocytes. Patients with CGD may present with recurrent, life-threatening bacterial or fungal infections and often need repeated hospitalization as early as infancy. We report a case of a boy aged 3 years and 1 month with a history of oral thrush, chronic diarrhea, skin abscesses, multiple small joints osteomyelitis, and multiple liver abscesses since 2 months of age. X-linked chronic granulomatous disease was diagnosed by nitroblue tetrazolium test and further confirmed by genetic study using single strand conformation polymorphism (SSCP) analysis and genomic DNA sequencing. Two episodes of aspergillosis with severe aspergillus lung empyema and life-threatening Klebsiella pneumoniae infections were noted in the first 2 years of life despite long-term prophylaxis with trimethoprim-sulfamethoxazole and itraconazole. Recombinant human interferon-gamma (rINF-gamma) 50 microg/m(2) subcutaneous injection 3 times per week was added after his last episode of severe infection. Thereafter, the boy had normal growth and development with no evidence of severe infection during 18 months of follow-up at our outpatient clinic.
慢性肉芽肿病(CGD)是一种遗传性吞噬障碍疾病,由中性粒细胞和单核细胞的氧化爆发活性缺陷引起。CGD患者可能会出现反复的、危及生命的细菌或真菌感染,并且早在婴儿期就常常需要反复住院治疗。我们报告一例3岁1个月大的男孩,自2个月大以来就有鹅口疮、慢性腹泻、皮肤脓肿、多个小关节骨髓炎和多个肝脓肿病史。通过硝基蓝四氮唑试验诊断为X连锁慢性肉芽肿病,并通过单链构象多态性(SSCP)分析和基因组DNA测序的基因研究进一步确诊。尽管长期使用甲氧苄啶-磺胺甲恶唑和伊曲康唑进行预防,但在生命的头2年里仍发生了2次曲霉病,伴有严重的曲霉性肺脓胸和危及生命的肺炎克雷伯菌感染。在他最后一次严重感染发作后,加用了重组人干扰素-γ(rINF-γ),剂量为50μg/m²,每周皮下注射3次。此后,在我们门诊随访的18个月中,该男孩生长发育正常,没有严重感染的迹象。