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Coexistence of double seropositivity for MPO antibody and anti-GBM antibody in ANCA-associated vasculitis concurrent with multiple myeloma: A case report

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Author(s)
Hyeonjeong LeeJaeseok YangJinykung KwonMihwa HeoYaerim KimJin Hyuk PaekHyeongchan ShinMisun ChoeSeungyeup HanKyubok Jin
Alternative Author(s)
Heo, Mi HwaKim, Yae RimPaek, Jin HyukShin, Hyeong ChanChoe, Mi SunHan, Seung YeupJin, Kyu Bok
Department
Dept. of Internal Medicine (내과학)
Dept. of Pathology (병리학)
Journal Title
Medicine (Baltimore)
Issued Date
2024
Volume
103
Number
30
Keyword
ANCA-associated vasculitisanti-GBM antibodycase reportMPO antibodymultiple myeloma
Abstract
Rationale:
Immune-mediated vasculitis with 2 or more autoantibodies, for example, anti-proteinase-3, combined with anti-myeloperoxidase (MPO) or anti-glomerular basement membrane (GBM) antibodies, is extremely unusual. Furthermore, the coexistence of autoimmune vasculitis and hematological malignancies is uncommon. Herein, we describe a case of double-seropositive anti-neutrophil cytoplasmic antibody (ANCA) vasculitis with multiple myeloma.

Patient concerns:
A 79-year-old Asian man presented with persistent leg edema and kidney dysfunction. His kidney function rapidly decreased, and serologic test results showed higher titers of the anti-MPO antibody (54.7 IU/mL) and anti-GBM antibodies (>200 IU/mL). Additionally, the clinical features showed the possibility of monoclonal gammopathy with anemia and hyperglobulinemia. We performed kidney and bone marrow biopsy. Serum protein electrophoresis and immunofixation revealed no significant differences, but the results of the bone marrow smear were compatible with those of myeloma with 15% plasmacytosis. However, kidney biopsy showed diffuse crescentic glomerulonephritis without deposition of the immune complex or kappa/lambda chain.

Diagnoses and Interventions:
Finally, the patient was diagnosed with double-seropositive ANCA-associated glomerulonephritis and multiple myeloma. Given the patient’s performance status, we initiated low-dose steroid pulse therapy, followed by conservative management.

Outcomes:
While the pulmonary lesions showed improvement, the kidney function did not regain its previous state, prompting the initiation of kidney replacement therapy by hemodialysis. There has been a decrease in the levels of anti-GBM and anti-MPO antibodies since the initial diagnosis.

Lessons:
This case elucidates the complex interplay between ANCA-associated glomerulonephritis and hematologic malignancy and emphasizes the need for a nuanced treatment strategy considering its multifaceted clinical presentation.
Affiliated Author(s)
허미화
김예림
백진혁
신형찬
최미선
한승엽
진규복
Publisher
School of Medicine (의과대학)
Type
Article
ISSN
0025-7974
Fulltext
https://journals.lww.com/md-journal/fulltext/2024/07260/coexistence_of_double_seropositivity_for_mpo.8.aspx
DOI
10.1097/MD.0000000000039021
URI
https://kumel.medlib.dsmc.or.kr/handle/2015.oak/45801
Appears in Collections:
1. School of Medicine (의과대학) > Dept. of Internal Medicine (내과학)
1. School of Medicine (의과대학) > Dept. of Pathology (병리학)
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