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Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report

BACKGROUND: The literature describes a case of systemic lupus erythematosus (SLE) complicated with Castleman’s disease (CD) and secondary paraneoplastic pemphigus (PNP). CASE PRESENTATION: A 12-year-old female presented with a neck mass, rash, arthralgia, and skin and mouth ulceration for 5 years we...

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Autores principales: Ma, Xin, Li, Jiyuan, Fan, Linlin, Jiang, Hongwei, Shi, Gaishao, Ge, Dongfeng, Shi, Xiaofei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588252/
https://www.ncbi.nlm.nih.gov/pubmed/37858241
http://dx.doi.org/10.1186/s12969-023-00871-2
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author Ma, Xin
Li, Jiyuan
Fan, Linlin
Jiang, Hongwei
Shi, Gaishao
Ge, Dongfeng
Shi, Xiaofei
author_facet Ma, Xin
Li, Jiyuan
Fan, Linlin
Jiang, Hongwei
Shi, Gaishao
Ge, Dongfeng
Shi, Xiaofei
author_sort Ma, Xin
collection PubMed
description BACKGROUND: The literature describes a case of systemic lupus erythematosus (SLE) complicated with Castleman’s disease (CD) and secondary paraneoplastic pemphigus (PNP). CASE PRESENTATION: A 12-year-old female presented with a neck mass, rash, arthralgia, and skin and mouth ulceration for 5 years were admitted. All blood cells were low. Multiple autoantibodies associated with SLE were positive. The pathology of the neck mass revealed the classical manifestations of CD. She was treated with prednisone, hydroxychloroquine, leflunomide, thalidomide, and dressings. Pathological examination of the skin revealed PNP. The neck mass was removed and continued to take antirheumatic drugs. At subsequent follow-up, the patient’s disease status was stable and the skin mucosal lesion did not recur. CONCLUSION: The case of simultaneous SLE, CD, and PNP in children was rarely reported, and the correct diagnosis of the disease will help to take timely treatment.
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spelling pubmed-105882522023-10-21 Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report Ma, Xin Li, Jiyuan Fan, Linlin Jiang, Hongwei Shi, Gaishao Ge, Dongfeng Shi, Xiaofei Pediatr Rheumatol Online J Case Report BACKGROUND: The literature describes a case of systemic lupus erythematosus (SLE) complicated with Castleman’s disease (CD) and secondary paraneoplastic pemphigus (PNP). CASE PRESENTATION: A 12-year-old female presented with a neck mass, rash, arthralgia, and skin and mouth ulceration for 5 years were admitted. All blood cells were low. Multiple autoantibodies associated with SLE were positive. The pathology of the neck mass revealed the classical manifestations of CD. She was treated with prednisone, hydroxychloroquine, leflunomide, thalidomide, and dressings. Pathological examination of the skin revealed PNP. The neck mass was removed and continued to take antirheumatic drugs. At subsequent follow-up, the patient’s disease status was stable and the skin mucosal lesion did not recur. CONCLUSION: The case of simultaneous SLE, CD, and PNP in children was rarely reported, and the correct diagnosis of the disease will help to take timely treatment. BioMed Central 2023-10-19 /pmc/articles/PMC10588252/ /pubmed/37858241 http://dx.doi.org/10.1186/s12969-023-00871-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Ma, Xin
Li, Jiyuan
Fan, Linlin
Jiang, Hongwei
Shi, Gaishao
Ge, Dongfeng
Shi, Xiaofei
Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title_full Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title_fullStr Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title_full_unstemmed Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title_short Systemic lupus erythematosus combined with Castleman disease and secondary paraneoplastic pemphigus: a case report
title_sort systemic lupus erythematosus combined with castleman disease and secondary paraneoplastic pemphigus: a case report
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10588252/
https://www.ncbi.nlm.nih.gov/pubmed/37858241
http://dx.doi.org/10.1186/s12969-023-00871-2
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