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Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies
Paraneoplastic pemphigus (PNP) is a severe autoimmune syndrome commonly triggered by neoplasms. The prognosis of CLL-associated PNP is dismal due to its refractory course and secondary infection and no standard treatment was recommended. We retrospectively reported six CLL with PNP cases from 842 ca...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529904/ https://www.ncbi.nlm.nih.gov/pubmed/33004832 http://dx.doi.org/10.1038/s41598-020-73131-y |
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author | Cao, Lei Wang, Fei Du, Xin-Yi Zhu, Hua-Yuan Wang, Li Xu, Wei Li, Jian-Yong Fan, Lei |
author_facet | Cao, Lei Wang, Fei Du, Xin-Yi Zhu, Hua-Yuan Wang, Li Xu, Wei Li, Jian-Yong Fan, Lei |
author_sort | Cao, Lei |
collection | PubMed |
description | Paraneoplastic pemphigus (PNP) is a severe autoimmune syndrome commonly triggered by neoplasms. The prognosis of CLL-associated PNP is dismal due to its refractory course and secondary infection and no standard treatment was recommended. We retrospectively reported six CLL with PNP cases from 842 cases of CLL including diagnosis, treatment and prognosis. The median time between the initial of CLL to PNP was 36 months while the median overall survival from the diagnosis of PNP was 26 months. And three cases died of lung infection while 5 developed pulmonary symptoms. And 5 cases received fludarabine-based chemotherapy before developing PNP, which suggesting fludarabine was one of potential causes of PNP. For the treatment, five patients were rescued by combined regimens including rituximab, methylprednisolone, immunoglobulin, fresh frozen plasma and the last received ibrutinib combined with short-term prednisone. Fludarabine-based regimen may be one of the potential causes of PNP. The combined regimen might shed a new light, while ibrutinib is a promising drug for CLL with PNP, but needs much more evidence. PNP should be carefully treated to guide early diagnosis and intervention for a better prognosis. |
format | Online Article Text |
id | pubmed-7529904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75299042020-10-02 Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies Cao, Lei Wang, Fei Du, Xin-Yi Zhu, Hua-Yuan Wang, Li Xu, Wei Li, Jian-Yong Fan, Lei Sci Rep Article Paraneoplastic pemphigus (PNP) is a severe autoimmune syndrome commonly triggered by neoplasms. The prognosis of CLL-associated PNP is dismal due to its refractory course and secondary infection and no standard treatment was recommended. We retrospectively reported six CLL with PNP cases from 842 cases of CLL including diagnosis, treatment and prognosis. The median time between the initial of CLL to PNP was 36 months while the median overall survival from the diagnosis of PNP was 26 months. And three cases died of lung infection while 5 developed pulmonary symptoms. And 5 cases received fludarabine-based chemotherapy before developing PNP, which suggesting fludarabine was one of potential causes of PNP. For the treatment, five patients were rescued by combined regimens including rituximab, methylprednisolone, immunoglobulin, fresh frozen plasma and the last received ibrutinib combined with short-term prednisone. Fludarabine-based regimen may be one of the potential causes of PNP. The combined regimen might shed a new light, while ibrutinib is a promising drug for CLL with PNP, but needs much more evidence. PNP should be carefully treated to guide early diagnosis and intervention for a better prognosis. Nature Publishing Group UK 2020-10-01 /pmc/articles/PMC7529904/ /pubmed/33004832 http://dx.doi.org/10.1038/s41598-020-73131-y Text en © The Author(s) 2020 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/. |
spellingShingle | Article Cao, Lei Wang, Fei Du, Xin-Yi Zhu, Hua-Yuan Wang, Li Xu, Wei Li, Jian-Yong Fan, Lei Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title | Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title_full | Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title_fullStr | Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title_full_unstemmed | Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title_short | Chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
title_sort | chronic lymphocytic leukemia-associated paraneoplastic pemphigus: potential cause and therapeutic strategies |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529904/ https://www.ncbi.nlm.nih.gov/pubmed/33004832 http://dx.doi.org/10.1038/s41598-020-73131-y |
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