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Suspected Frequent Relapsing IgG4-related Lung Disease in Kidney Transplant Patient: A Case Report

Authors
Kim, A. J.Ro, H.Chang, J. H.Jung, J. Y.Chung, W. K.Park, Y. H.Lee, H. H.
Issue Date
Oct-2018
Publisher
ELSEVIER SCIENCE INC
Citation
TRANSPLANTATION PROCEEDINGS, v.50, no.8, pp.2572 - 2574
Journal Title
TRANSPLANTATION PROCEEDINGS
Volume
50
Number
8
Start Page
2572
End Page
2574
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/3251
DOI
10.1016/j.transproceed.2018.02.197
ISSN
0041-1345
Abstract
Besides the initial description of IgG4-related pancreatic disease, other sites are now commonly involved. However, occurrence of IgG4-related disease is rare in organ transplanted patients. A 57-year-old man who received a kidney transplantation presented with recurrent dyspnea on exertion. A computed tomography scan of the chest revealed bilateral interlobular septal thickening and multiple tubular and branching small nodular lesions in the right upper lobe, and mass-like consolidation of the left middle lobe. Despite no elevation of serum IgG4 level, a percutaneous core needle biopsy on consolidative mass showed interstitial fibrosis and infiltration of IgG4-positive plasma cells to be more than > 20 per high power field. After treatment with glucocorticoids and rituximab, the consolidative mass of the left middle lobe disappeared.
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