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Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis

BACKGROUND: Granulomatosis with polyangiitis (GPA) is an anti-neutrophilic cytoplasmic antibody-associated vasculitis affecting small to medium-sized vessels and involves most commonly the kidneys and the respiratory tract. Skin involvement can be seen in up to 50% of children with GPA and is the in...

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Autores principales: Oz, Rotem Semo, Onajin, Oluwakemi, Harel, Liora, Tal, Rotem, Dallos, Tomas, Rosenblatt, Adena, Plank, Lukas, Wagner-Weiner, Linda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180159/
https://www.ncbi.nlm.nih.gov/pubmed/34090470
http://dx.doi.org/10.1186/s12969-021-00564-8
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author Oz, Rotem Semo
Onajin, Oluwakemi
Harel, Liora
Tal, Rotem
Dallos, Tomas
Rosenblatt, Adena
Plank, Lukas
Wagner-Weiner, Linda
author_facet Oz, Rotem Semo
Onajin, Oluwakemi
Harel, Liora
Tal, Rotem
Dallos, Tomas
Rosenblatt, Adena
Plank, Lukas
Wagner-Weiner, Linda
author_sort Oz, Rotem Semo
collection PubMed
description BACKGROUND: Granulomatosis with polyangiitis (GPA) is an anti-neutrophilic cytoplasmic antibody-associated vasculitis affecting small to medium-sized vessels and involves most commonly the kidneys and the respiratory tract. Skin involvement can be seen in up to 50% of children with GPA and is the initial presenting symptom in 7.7%. Pyoderma gangrenosum (PG)-like ulcers are rarely described as a skin manifestation in GPA and very few cases have been reported previously in children. CASE PRESENTATION: We describe 3 new pediatric cases of GPA with PG-like ulcerations. The median age at first symptom was 15 years. Two patients had PG-like ulceration as their initial presentation; additional symptoms eventually led to the diagnosis of GPA 2–24 months later. In 1 case, proteinase 3 (PR3) was negative when first tested, but converted to positive when systemic symptoms emerged; in the other 2 cases PR3 was positive at presentation. All 3 patients had prominent facial lesions. None of the patients responded to treatment with antibiotics or medications commonly used to manage PG, including corticosteroids and cyclosporine. All patients had excellent responses to rituximab. An electronic database literature review was performed and 4 previously reported cases were identified. We assessed the clinical characteristics, serology, and response to treatment of the previously reported and our newly diagnosed cases. CONCLUSION: PG-like ulceration is a rare presentation of pediatric GPA which may precede classic systemic GPA symptoms. The predominance of facial ulcer, granulomatous and neutrophilic inflammation on skin biopsy and lack of response to PG treatments are characteristic of GPA-associated PG-like ulcers. Our review suggests that treatment with rituximab may be needed to improve the skin lesions. Recognizing that PG-like ulcerations can occur in pediatric GPA may result in timely diagnosis, appropriate treatment and improved prognosis.
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spelling pubmed-81801592021-06-07 Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis Oz, Rotem Semo Onajin, Oluwakemi Harel, Liora Tal, Rotem Dallos, Tomas Rosenblatt, Adena Plank, Lukas Wagner-Weiner, Linda Pediatr Rheumatol Online J Case Report BACKGROUND: Granulomatosis with polyangiitis (GPA) is an anti-neutrophilic cytoplasmic antibody-associated vasculitis affecting small to medium-sized vessels and involves most commonly the kidneys and the respiratory tract. Skin involvement can be seen in up to 50% of children with GPA and is the initial presenting symptom in 7.7%. Pyoderma gangrenosum (PG)-like ulcers are rarely described as a skin manifestation in GPA and very few cases have been reported previously in children. CASE PRESENTATION: We describe 3 new pediatric cases of GPA with PG-like ulcerations. The median age at first symptom was 15 years. Two patients had PG-like ulceration as their initial presentation; additional symptoms eventually led to the diagnosis of GPA 2–24 months later. In 1 case, proteinase 3 (PR3) was negative when first tested, but converted to positive when systemic symptoms emerged; in the other 2 cases PR3 was positive at presentation. All 3 patients had prominent facial lesions. None of the patients responded to treatment with antibiotics or medications commonly used to manage PG, including corticosteroids and cyclosporine. All patients had excellent responses to rituximab. An electronic database literature review was performed and 4 previously reported cases were identified. We assessed the clinical characteristics, serology, and response to treatment of the previously reported and our newly diagnosed cases. CONCLUSION: PG-like ulceration is a rare presentation of pediatric GPA which may precede classic systemic GPA symptoms. The predominance of facial ulcer, granulomatous and neutrophilic inflammation on skin biopsy and lack of response to PG treatments are characteristic of GPA-associated PG-like ulcers. Our review suggests that treatment with rituximab may be needed to improve the skin lesions. Recognizing that PG-like ulcerations can occur in pediatric GPA may result in timely diagnosis, appropriate treatment and improved prognosis. BioMed Central 2021-06-05 /pmc/articles/PMC8180159/ /pubmed/34090470 http://dx.doi.org/10.1186/s12969-021-00564-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Oz, Rotem Semo
Onajin, Oluwakemi
Harel, Liora
Tal, Rotem
Dallos, Tomas
Rosenblatt, Adena
Plank, Lukas
Wagner-Weiner, Linda
Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title_full Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title_fullStr Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title_full_unstemmed Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title_short Pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
title_sort pyoderma gangrenosum-like ulceration as a presenting feature of pediatric granulomatosis with polyangiitis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180159/
https://www.ncbi.nlm.nih.gov/pubmed/34090470
http://dx.doi.org/10.1186/s12969-021-00564-8
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