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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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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. |
format | Online Article Text |
id | pubmed-10588252 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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