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Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a severe clinical entity associated with high mortality in the adult population. HLH has been associated with infections, malignancy and autoimmune conditions such as Systemic Lupus Erythematosus (SLE), however this is often in the context of a...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390523/ https://www.ncbi.nlm.nih.gov/pubmed/30886995 http://dx.doi.org/10.1186/s41927-019-0055-x |
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author | Thornton, Christina S. Minoo, Parham Schneider, Michelle Fifi-Mah, Aurore |
author_facet | Thornton, Christina S. Minoo, Parham Schneider, Michelle Fifi-Mah, Aurore |
author_sort | Thornton, Christina S. |
collection | PubMed |
description | BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a severe clinical entity associated with high mortality in the adult population. HLH has been associated with infections, malignancy and autoimmune conditions such as Systemic Lupus Erythematosus (SLE), however this is often in the context of a disease flare. Currently, there are limited reports of inaugural SLE manifesting as HLH with a lack of consensus on treatment and management of these patients. CASE PRESENTATION: Here, we present two rare case reports of severe cutaneous manifestation of lupus associated with HLH. Both patients presented with sinister clinical courses with primarily rheumatologic complaints including malaise, arthralgia, and myalgia with biochemical abnormalities. Both patients were diagnosed with HLH as a result of first presentation from cutaneous lupus. A comprehensive literature review using the PubMed database with cases comprising keywords of HLH and SLE up to September 2017 was conducted, with an emphasis on inaugural cutaneous SLE cases. CONCLUSIONS: Ultimately, we highlight that a keen clinical acumen is required as misdiagnosis may lead to insufficient treatment with adverse clinical outcomes with the unique presentation of HLH from inaugural cases of SLE. |
format | Online Article Text |
id | pubmed-6390523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-63905232019-03-18 Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature Thornton, Christina S. Minoo, Parham Schneider, Michelle Fifi-Mah, Aurore BMC Rheumatol Case Report BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a severe clinical entity associated with high mortality in the adult population. HLH has been associated with infections, malignancy and autoimmune conditions such as Systemic Lupus Erythematosus (SLE), however this is often in the context of a disease flare. Currently, there are limited reports of inaugural SLE manifesting as HLH with a lack of consensus on treatment and management of these patients. CASE PRESENTATION: Here, we present two rare case reports of severe cutaneous manifestation of lupus associated with HLH. Both patients presented with sinister clinical courses with primarily rheumatologic complaints including malaise, arthralgia, and myalgia with biochemical abnormalities. Both patients were diagnosed with HLH as a result of first presentation from cutaneous lupus. A comprehensive literature review using the PubMed database with cases comprising keywords of HLH and SLE up to September 2017 was conducted, with an emphasis on inaugural cutaneous SLE cases. CONCLUSIONS: Ultimately, we highlight that a keen clinical acumen is required as misdiagnosis may lead to insufficient treatment with adverse clinical outcomes with the unique presentation of HLH from inaugural cases of SLE. BioMed Central 2019-02-08 /pmc/articles/PMC6390523/ /pubmed/30886995 http://dx.doi.org/10.1186/s41927-019-0055-x Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Case Report Thornton, Christina S. Minoo, Parham Schneider, Michelle Fifi-Mah, Aurore Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title | Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title_full | Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title_fullStr | Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title_full_unstemmed | Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title_short | Severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
title_sort | severe skin disease in lupus associated with hemophagocytic lymphohistiocytosis: case reports and review of the literature |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390523/ https://www.ncbi.nlm.nih.gov/pubmed/30886995 http://dx.doi.org/10.1186/s41927-019-0055-x |
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