Journal Basic Info
- Impact Factor: 1.809**
- H-Index: 6
- ISSN: 2474-1655
- DOI: 10.25107/2474-1655
Major Scope
- Pediatrics
- Orthopedic Surgery
- Surgery Cases
- Renal Disease
- Epidemiology
- Endocrinology
- Pharmacology and Therapeutics
- Tuberculosis
Abstract
Citation: Ann Clin Case Rep. 2019;4(1):1586.DOI: 10.25107/2474-1655.1586
IgG4-Related Interstitial Lung Disease and Lymphadenopathy: Report of a Case
Bing Xiao, Fang Wan, Hongliang Zhang, Zhibiao He, Xiangping Chai and Xudong Xiang
Department of Emergency Medicine, The Second Xiangya Hospital of Central South University, China
*Correspondance to: Xudong Xiang
PDF Full Text Case Report | Open Access
Abstract:
IgG4-related disease is an immune-related condition that can affect multiple organ systems. Since it was first described in 2003, this heterogeneous disease had gained much attention, but the general acknowledgement of this disease remained relatively low, so misdiagnoses are common during clinical practice. Here we report a case of a 41-year-old female patient with recurrent lymphadenopathy, rash on her limbs and aggravating dyspnea, who suffered from these symptoms for 5 years before she was finally diagnosed with IgG4-related interstitial lung disease and lymphadenopathy.
Keywords:
Cite the Article:
Xiao B, Wan F, Zhang H, He Z, Chai X, Xiang X. IgG4-Related Interstitial Lung Disease and Lymphadenopathy: Report of a Case. Ann Clin Case Rep. 2019; 4: 1586.
