Tabarsi Payam, Mirsaeidi Mehdi, Karimi Shirin, Banieghbal Behzad, Mansouri Nahal, Masjedi Mohammad Reza, Mansouri Davood
National Research Institute of TB and Lung disease, Niavaran-Darabad, Massih Daneshvari Hospital, Tehran, Iran.
Iran J Allergy Asthma Immunol. 2007 Dec;6(4):219-21.
Chronic Granulomatous Disease (CGD) is a rare primary immunodeficiency disease. Although the most affected patients are diagnosed in childhood, there are several reports of the disease presenting in adult patients. Here we present a 40 years old man who was admitted in hospital due to respiratory symptoms and ground glass pattern in high resolution computed tomography of lung. Open lung biopsy revealed lymphocytic bronchiolitis. Because of past medical history of granulomatous lesion in lung and recurrent abscesses of skin and soft tissue, NBT test was conducted which its result revealed that the disorder was compatible with CGD and then it was confirmed by fluorescent cytometry.
慢性肉芽肿病(CGD)是一种罕见的原发性免疫缺陷病。尽管大多数受影响的患者在儿童期被诊断,但也有几例该疾病在成年患者中出现的报道。在此,我们报告一名40岁男性,因呼吸道症状和肺部高分辨率计算机断层扫描显示磨玻璃影而入院。开胸肺活检显示淋巴细胞性细支气管炎。由于既往有肺部肉芽肿病变及皮肤和软组织反复脓肿病史,进行了硝基四氮唑蓝(NBT)试验,结果显示该疾病与CGD相符,随后通过荧光细胞术得以确诊。