Winkelstein J A, Marino M C, Johnston R B, Boyle J, Curnutte J, Gallin J I, Malech H L, Holland S M, Ochs H, Quie P, Buckley R H, Foster C B, Chanock S J, Dickler H
Immune Deficiency Foundation, Baltimore, Maryland, USA.
Medicine (Baltimore). 2000 May;79(3):155-69. doi: 10.1097/00005792-200005000-00003.
A registry of United States residents with chronic granulomatous disease (CGD) was established in 1993 in order to estimate the minimum incidence of this uncommon primary immunodeficiency disease and characterize its epidemiologic and clinical features. To date, 368 patients have been registered; 259 have the X-linked recessive form of CGD, 81 have 1 of the autosomal recessive forms, and in 28 the mode of inheritance is unknown. The minimum estimate of birth rate is between 1/200,000 and 1/250,000 live births for the period 1980-1989. Pneumonia was the most prevalent infection (79% of patients; Aspergillus most prevalent cause), followed by suppurative adenitis (53% of patients; Staphylococcus most prevalent cause), subcutaneous abscess (42% of patients; Staphylococcus most prevalent cause), liver abscess (27% of patients; Staphylococcus most prevalent cause), osteomyelitis (25% of patients; Serratia most prevalent cause), and sepsis (18% of patients; Salmonella most prevalent cause). Fifteen percent of patients had gastric outlet obstruction, 10% urinary tract obstruction, and 17% colitis/enteritis. Ten percent of X-linked recessive kindreds and 3% of autosomal recessive kindreds had family members with lupus. Eighteen percent of patients either were deceased when registered or died after being registered. The most common causes of death were pneumonia and/or sepsis due to Aspergillus (23 patients) or Burkholderia cepacia (12 patients). Patients with the X-linked recessive form of the disease appear to have a more serious clinical phenotype than patients with the autosomal recessive forms of the disease, based on the fact that they are diagnosed significantly earlier (mean, 3.01 years of age versus 7.81 years of age, respectively), have a significantly higher prevalence of perirectal abscess (17% versus 7%), suppurative adenitis (59% versus 32%), bacteremia/fungemia (21% versus 10%), gastric obstruction (19% versus 5%), and urinary tract obstruction (11% versus 3%), and a higher mortality (21.2% versus 8.6%).
1993年建立了美国慢性肉芽肿病(CGD)患者登记处,以估计这种罕见的原发性免疫缺陷疾病的最低发病率,并描述其流行病学和临床特征。迄今为止,已登记368例患者;259例为X连锁隐性形式的CGD,81例为常染色体隐性形式之一,28例的遗传方式未知。1980 - 1989年期间,最低出生率估计为每20万至25万活产中有1例。肺炎是最常见的感染(79%的患者;最常见病因是曲霉菌),其次是化脓性腺炎(53%的患者;最常见病因是葡萄球菌)、皮下脓肿(42%的患者;最常见病因是葡萄球菌)、肝脓肿(27%的患者;最常见病因是葡萄球菌)、骨髓炎(25%的患者;最常见病因是沙雷氏菌)和败血症(18%的患者;最常见病因是沙门氏菌)。15%的患者有胃出口梗阻,10%有尿路梗阻,17%有结肠炎/肠炎。10%的X连锁隐性家族和3%常染色体隐性家族有狼疮患者。18%的患者在登记时已死亡或登记后死亡。最常见的死亡原因是曲霉菌(23例患者)或洋葱伯克霍尔德菌(12例患者)引起的肺炎和/或败血症。基于以下事实,患有X连锁隐性形式疾病的患者似乎比患有常染色体隐性形式疾病的患者具有更严重的临床表型:他们被诊断的时间明显更早(平均年龄分别为3.01岁和7.81岁),肛周脓肿(17%对7%)、化脓性腺炎(59%对32%)、菌血症/真菌血症(21%对10%)、胃梗阻(19%对5%)和尿路梗阻(11%对3%)的患病率明显更高,死亡率也更高(21.2%对8.6%)。