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Multicentric Reticulohistiocytosis–A rare and disabling disease
Multicentric reticulohistiocytosis is a rare multisystemic condition associated with papulonodular skin lesions, severe arthritis and malignancy. Histopathology shows histiocytes containing abundant eosinophilic ground glass cytoplasm and multinucleated giant cells. Early recognition, age‐appropriat...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460929/ https://www.ncbi.nlm.nih.gov/pubmed/37645054 http://dx.doi.org/10.1002/ccr3.7846 |
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author | Ashaolu, Omowunmi Ng, Selwyn Smale, Shaun Hughes, Jenny |
author_facet | Ashaolu, Omowunmi Ng, Selwyn Smale, Shaun Hughes, Jenny |
author_sort | Ashaolu, Omowunmi |
collection | PubMed |
description | Multicentric reticulohistiocytosis is a rare multisystemic condition associated with papulonodular skin lesions, severe arthritis and malignancy. Histopathology shows histiocytes containing abundant eosinophilic ground glass cytoplasm and multinucleated giant cells. Early recognition, age‐appropriate malignancy work‐up and treatment is important to prevent impairment of daily life activity. |
format | Online Article Text |
id | pubmed-10460929 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104609292023-08-29 Multicentric Reticulohistiocytosis–A rare and disabling disease Ashaolu, Omowunmi Ng, Selwyn Smale, Shaun Hughes, Jenny Clin Case Rep Case Report Multicentric reticulohistiocytosis is a rare multisystemic condition associated with papulonodular skin lesions, severe arthritis and malignancy. Histopathology shows histiocytes containing abundant eosinophilic ground glass cytoplasm and multinucleated giant cells. Early recognition, age‐appropriate malignancy work‐up and treatment is important to prevent impairment of daily life activity. John Wiley and Sons Inc. 2023-08-27 /pmc/articles/PMC10460929/ /pubmed/37645054 http://dx.doi.org/10.1002/ccr3.7846 Text en © 2023 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Ashaolu, Omowunmi Ng, Selwyn Smale, Shaun Hughes, Jenny Multicentric Reticulohistiocytosis–A rare and disabling disease |
title | Multicentric Reticulohistiocytosis–A rare and disabling disease |
title_full | Multicentric Reticulohistiocytosis–A rare and disabling disease |
title_fullStr | Multicentric Reticulohistiocytosis–A rare and disabling disease |
title_full_unstemmed | Multicentric Reticulohistiocytosis–A rare and disabling disease |
title_short | Multicentric Reticulohistiocytosis–A rare and disabling disease |
title_sort | multicentric reticulohistiocytosis–a rare and disabling disease |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10460929/ https://www.ncbi.nlm.nih.gov/pubmed/37645054 http://dx.doi.org/10.1002/ccr3.7846 |
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