Yalçin I, Güler N, Oneş U, Salman N, Anak S
Department of Pediatrics, Istanbul University Faculty of Medicine.
Turk J Pediatr. 1990 Jan-Mar;32(1):43-7.
An eleven-year-old boy with a history of severe lung infection which had been resistant to antibiotic therapy for a period of six months demonstrated a functional leukocyte defect similar to that found in children with chronic granulomatous disease (CGD). X-ray findings suggested a hilar mass, and granulomatous lesions developed on the thorax wall. The documentation of this case suggests that there may be a late presenting form of CGD.
一名11岁男孩,有严重肺部感染病史,对抗生素治疗耐药达6个月,表现出与慢性肉芽肿病(CGD)患儿相似的功能性白细胞缺陷。X线检查结果提示肺门肿块,胸壁出现肉芽肿性病变。该病例记录表明可能存在CGD的迟发型。