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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...

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Detalles Bibliográficos
Autores principales: Ashaolu, Omowunmi, Ng, Selwyn, Smale, Shaun, Hughes, Jenny
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
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.
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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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