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ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review
BACKGROUND: Systemic sclerosis (SSc) and anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) both affect the kidney and may cause renal failure. Treatment of AAV is dramatically different from that of SSc renal crisis (SRC). Kidney biopsy is not recommended for diagnosing SRC, bu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011393/ https://www.ncbi.nlm.nih.gov/pubmed/33789719 http://dx.doi.org/10.1186/s40001-021-00500-2 |
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author | Wu, Rui Su, Jiang Zou, Yu-rong Zhu, Jing |
author_facet | Wu, Rui Su, Jiang Zou, Yu-rong Zhu, Jing |
author_sort | Wu, Rui |
collection | PubMed |
description | BACKGROUND: Systemic sclerosis (SSc) and anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) both affect the kidney and may cause renal failure. Treatment of AAV is dramatically different from that of SSc renal crisis (SRC). Kidney biopsy is not recommended for diagnosing SRC, but it is the only reliable diagnostic method for AAV. CASE PRESENTATION: Here, a 49-year-old male patient with diffuse SSc presented with acute renal insufficiency and detectable ANCA with myeloperoxidase-specific antibodies. A renal biopsy revealed necrotizing glomerulonephritis and was consistent with AAV. This finding confirms the existence of AAV and SSc overlap syndrome. The patient was treated with intravenous methylprednisolone, intravenous cyclophosphamide, tandem membrane plasma exchange, and hemodialysis. After treatment, his clinical symptoms remained stable, and his creatinine and C-reactive protein (CRP) levels have remained normalized as of his most recent follow-up after hospital discharge. CONCLUSIONS: AAV can overlap with SSc; although this condition is rare, it is associated with considerable morbidity and mortality. Therefore, it is critical to recognize AAV in the setting of worsening renal function due to SSs and provide appropriate treatment. Several clinical features are suggestive of AAV rather than SRC, but renal biopsy is required for accurate diagnosis. |
format | Online Article Text |
id | pubmed-8011393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-80113932021-04-01 ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review Wu, Rui Su, Jiang Zou, Yu-rong Zhu, Jing Eur J Med Res Case Report BACKGROUND: Systemic sclerosis (SSc) and anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) both affect the kidney and may cause renal failure. Treatment of AAV is dramatically different from that of SSc renal crisis (SRC). Kidney biopsy is not recommended for diagnosing SRC, but it is the only reliable diagnostic method for AAV. CASE PRESENTATION: Here, a 49-year-old male patient with diffuse SSc presented with acute renal insufficiency and detectable ANCA with myeloperoxidase-specific antibodies. A renal biopsy revealed necrotizing glomerulonephritis and was consistent with AAV. This finding confirms the existence of AAV and SSc overlap syndrome. The patient was treated with intravenous methylprednisolone, intravenous cyclophosphamide, tandem membrane plasma exchange, and hemodialysis. After treatment, his clinical symptoms remained stable, and his creatinine and C-reactive protein (CRP) levels have remained normalized as of his most recent follow-up after hospital discharge. CONCLUSIONS: AAV can overlap with SSc; although this condition is rare, it is associated with considerable morbidity and mortality. Therefore, it is critical to recognize AAV in the setting of worsening renal function due to SSs and provide appropriate treatment. Several clinical features are suggestive of AAV rather than SRC, but renal biopsy is required for accurate diagnosis. BioMed Central 2021-03-31 /pmc/articles/PMC8011393/ /pubmed/33789719 http://dx.doi.org/10.1186/s40001-021-00500-2 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Wu, Rui Su, Jiang Zou, Yu-rong Zhu, Jing ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title | ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title_full | ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title_fullStr | ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title_full_unstemmed | ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title_short | ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
title_sort | anca-associated vasculitis overlaps with systemic sclerosis: a case report and literature review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8011393/ https://www.ncbi.nlm.nih.gov/pubmed/33789719 http://dx.doi.org/10.1186/s40001-021-00500-2 |
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