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Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review

Hypocomplementemic urticarial vasculitis syndrome (HUVS), or McDuffie syndrome, is a rare small vessel vasculitis associated with urticaria, hypocomplementemia and positivity of anti-C1q antibodies. In rare cases, HUVS can manifest as an immune-complex mediated glomerulonephritis with a membranoprol...

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Autores principales: Ion, Oana, Obrișcă, Bogdan, Ismail, Gener, Sorohan, Bogdan, Bălănică, Sonia, Mircescu, Gabriel, Sinescu, Ioanel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408727/
https://www.ncbi.nlm.nih.gov/pubmed/32640739
http://dx.doi.org/10.3390/jcm9072131
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author Ion, Oana
Obrișcă, Bogdan
Ismail, Gener
Sorohan, Bogdan
Bălănică, Sonia
Mircescu, Gabriel
Sinescu, Ioanel
author_facet Ion, Oana
Obrișcă, Bogdan
Ismail, Gener
Sorohan, Bogdan
Bălănică, Sonia
Mircescu, Gabriel
Sinescu, Ioanel
author_sort Ion, Oana
collection PubMed
description Hypocomplementemic urticarial vasculitis syndrome (HUVS), or McDuffie syndrome, is a rare small vessel vasculitis associated with urticaria, hypocomplementemia and positivity of anti-C1q antibodies. In rare cases, HUVS can manifest as an immune-complex mediated glomerulonephritis with a membranoproliferative pattern of injury. Due to the rarity of this disorder, little is known about the clinical manifestation, pathogenesis, treatment response and outcome of such patients. We describe here three cases of HUVS with severe renal involvement. These patients had a rapidly progressive form of glomerulonephritis with severe nephrotic syndrome against a background of a membranoproliferative pattern of glomerular injury with extensive crescent formation. Therefore, these patients required aggressive induction and maintenance immunosuppressive therapy, with a clinical and renal response in two patients, while the third patient progressed to end-stage renal disease. Because of the rarity of this condition, there are few data regarding the clinical presentation, pathology and outcome of such patients. Accordingly, we provide an extensive literature review of cases reported from 1976 until 2020 and place them in the context of the current knowledge of HUVS pathogenesis. We identified 60 patients with HUVS and renal involvement that had adequate clinical data reported, out of which 52 patients underwent a percutaneous kidney biopsy. The most frequent renal manifestation was hematuria associated with proteinuria (70% of patients), while one third had abnormal kidney function on presentation (estimated glomerular filtration (GFR) below 60 mL/min/1.73 m(2)). The most frequent glomerular pattern of injury was membranoproliferative (35%), followed by mesangioproliferative (21%) and membranous (19%). Similar to other systemic vasculitis, renal involvement carries a poorer prognosis, but the outcome can be improved by aggressive immunosuppressive treatment.
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spelling pubmed-74087272020-08-13 Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review Ion, Oana Obrișcă, Bogdan Ismail, Gener Sorohan, Bogdan Bălănică, Sonia Mircescu, Gabriel Sinescu, Ioanel J Clin Med Review Hypocomplementemic urticarial vasculitis syndrome (HUVS), or McDuffie syndrome, is a rare small vessel vasculitis associated with urticaria, hypocomplementemia and positivity of anti-C1q antibodies. In rare cases, HUVS can manifest as an immune-complex mediated glomerulonephritis with a membranoproliferative pattern of injury. Due to the rarity of this disorder, little is known about the clinical manifestation, pathogenesis, treatment response and outcome of such patients. We describe here three cases of HUVS with severe renal involvement. These patients had a rapidly progressive form of glomerulonephritis with severe nephrotic syndrome against a background of a membranoproliferative pattern of glomerular injury with extensive crescent formation. Therefore, these patients required aggressive induction and maintenance immunosuppressive therapy, with a clinical and renal response in two patients, while the third patient progressed to end-stage renal disease. Because of the rarity of this condition, there are few data regarding the clinical presentation, pathology and outcome of such patients. Accordingly, we provide an extensive literature review of cases reported from 1976 until 2020 and place them in the context of the current knowledge of HUVS pathogenesis. We identified 60 patients with HUVS and renal involvement that had adequate clinical data reported, out of which 52 patients underwent a percutaneous kidney biopsy. The most frequent renal manifestation was hematuria associated with proteinuria (70% of patients), while one third had abnormal kidney function on presentation (estimated glomerular filtration (GFR) below 60 mL/min/1.73 m(2)). The most frequent glomerular pattern of injury was membranoproliferative (35%), followed by mesangioproliferative (21%) and membranous (19%). Similar to other systemic vasculitis, renal involvement carries a poorer prognosis, but the outcome can be improved by aggressive immunosuppressive treatment. MDPI 2020-07-06 /pmc/articles/PMC7408727/ /pubmed/32640739 http://dx.doi.org/10.3390/jcm9072131 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ion, Oana
Obrișcă, Bogdan
Ismail, Gener
Sorohan, Bogdan
Bălănică, Sonia
Mircescu, Gabriel
Sinescu, Ioanel
Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title_full Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title_fullStr Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title_full_unstemmed Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title_short Kidney Involvement in Hypocomplementemic Urticarial Vasculitis Syndrome—A Case-Based Review
title_sort kidney involvement in hypocomplementemic urticarial vasculitis syndrome—a case-based review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408727/
https://www.ncbi.nlm.nih.gov/pubmed/32640739
http://dx.doi.org/10.3390/jcm9072131
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