Author/Authors :
Bemanian, Mohammad Hassan Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Bahrami, Sima Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Arshi, Saba Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Rezaeifar, Afshin Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Nabavi, Mohammad Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Fallahpour, Morteza Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran , Shokri, Sima Department of Allergy and Clinical Immunology - Rasoul Akram Hospital - Iran University of Medical Sciences - Tehran, Iran
Abstract :
Immunoglobulin G4-Related Disease (IgG4-RD) is a systemic fibroinflammatory
disease that has been proposed as a separate entity
since the beginning of this century. The disease is often manifested
by increased serum IgG4 levels and certain histopathological
manifestations. The patient mentioned in this article is a 29-yearold
man from Tajikistan, who has had a chronic cough since the
beginning of 2018 without a previous history of the disease. At
first, he was diagnosed with pneumonia for a long time and then
underwent a lung biopsy due to exacerbation of symptoms and
the spread of lung lesions in radiology but no abnormalities were
found in these evaluations. The patient traveled to Iran to continue
his treatment. He was re-evaluated and then the previous samples
taken from the patient’s lung tissue were re-examined. Here are the
key findings in favor of diagnosing IgG4 RD. Evaluations did not
confirm the involvement of other organs. He was first treated with
steroids and due to recurrence of symptoms, he was treated with
rituximab once which was significantly effective in improving the
patient’s clinical symptoms. In general, it can be concluded that the
diagnosis of IgG4-RD is very challenging and if it has not been
diagnosed and treated in time, it can lead to irreversible fibrosis and
permanent loss of function of the involved organ.