Histocytopathological diagnosis of Rosai–Dorfman disease: Case report

Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massiv...

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Autores principales: Abraham, Zephania Saitabau, Francis, Zerd, Ngaiza, Advera Isaac, Kahinga, Aveline Aloyce, Bukanu, Faustine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818281/
https://www.ncbi.nlm.nih.gov/pubmed/35145693
http://dx.doi.org/10.1002/ccr3.5412
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author Abraham, Zephania Saitabau
Francis, Zerd
Ngaiza, Advera Isaac
Kahinga, Aveline Aloyce
Bukanu, Faustine
author_facet Abraham, Zephania Saitabau
Francis, Zerd
Ngaiza, Advera Isaac
Kahinga, Aveline Aloyce
Bukanu, Faustine
author_sort Abraham, Zephania Saitabau
collection PubMed
description Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massive bilateral cervical and submandibular lymphadenopathy, diagnosed by histocytopathology.
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spelling pubmed-88182812022-02-09 Histocytopathological diagnosis of Rosai–Dorfman disease: Case report Abraham, Zephania Saitabau Francis, Zerd Ngaiza, Advera Isaac Kahinga, Aveline Aloyce Bukanu, Faustine Clin Case Rep Case Reports Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy. We are hereby reporting a case of RDD presenting with massive bilateral cervical and submandibular lymphadenopathy, diagnosed by histocytopathology. John Wiley and Sons Inc. 2022-02-06 /pmc/articles/PMC8818281/ /pubmed/35145693 http://dx.doi.org/10.1002/ccr3.5412 Text en © 2022 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 Reports
Abraham, Zephania Saitabau
Francis, Zerd
Ngaiza, Advera Isaac
Kahinga, Aveline Aloyce
Bukanu, Faustine
Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title_full Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title_fullStr Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title_full_unstemmed Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title_short Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
title_sort histocytopathological diagnosis of rosai–dorfman disease: case report
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8818281/
https://www.ncbi.nlm.nih.gov/pubmed/35145693
http://dx.doi.org/10.1002/ccr3.5412
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