پديد آورندگان :
Tabarsi Payam نويسنده , Mirsaeidi Seyed-Mehdi نويسنده , Karimi Shlrin نويسنده , Banieghbal Behzad نويسنده , Mansouri Nahal نويسنده , Masjedi Mohammad-Reza نويسنده , Mansouri Seyed-Davood نويسنده
چكيده لاتين :
Chronic Granulomatous Disease (CGO) 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 CGO and then it was confirmed by fluorescent cytometry