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Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement

Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented. T2W hypointense signal of the soft tissue masses was a distinguishing MRI feature. CONTRIBUTION: Rosai Dorf...

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Autores principales: Sharma, Smily, Sherwani, Poonam, Arunachalam, Venkata S., Dev, Rahul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AOSIS 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623647/
https://www.ncbi.nlm.nih.gov/pubmed/37928929
http://dx.doi.org/10.4102/sajr.v27i1.2729
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author Sharma, Smily
Sherwani, Poonam
Arunachalam, Venkata S.
Dev, Rahul
author_facet Sharma, Smily
Sherwani, Poonam
Arunachalam, Venkata S.
Dev, Rahul
author_sort Sharma, Smily
collection PubMed
description Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented. T2W hypointense signal of the soft tissue masses was a distinguishing MRI feature. CONTRIBUTION: Rosai Dorfman disease is often overlooked in the differentials of lymphadenopathy and soft tissue masses on account of its rarity. This case report comprehensively discusses the imaging approach to this rare disorder.
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spelling pubmed-106236472023-11-04 Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement Sharma, Smily Sherwani, Poonam Arunachalam, Venkata S. Dev, Rahul SA J Radiol Case Report Rosai Dorfman disease is a rare but benign and self-limiting disorder. A case of Rosai Dorfman disease in a 16-year-old female with classic radiological and pathological findings is presented. T2W hypointense signal of the soft tissue masses was a distinguishing MRI feature. CONTRIBUTION: Rosai Dorfman disease is often overlooked in the differentials of lymphadenopathy and soft tissue masses on account of its rarity. This case report comprehensively discusses the imaging approach to this rare disorder. AOSIS 2023-10-30 /pmc/articles/PMC10623647/ /pubmed/37928929 http://dx.doi.org/10.4102/sajr.v27i1.2729 Text en © 2023. The Authors https://creativecommons.org/licenses/by/4.0/Licensee: AOSIS. This work is licensed under the Creative Commons Attribution License.
spellingShingle Case Report
Sharma, Smily
Sherwani, Poonam
Arunachalam, Venkata S.
Dev, Rahul
Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title_full Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title_fullStr Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title_full_unstemmed Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title_short Revisiting Rosai Dorfman disease: A rare histiocytic disorder with nodal and extranodal involvement
title_sort revisiting rosai dorfman disease: a rare histiocytic disorder with nodal and extranodal involvement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10623647/
https://www.ncbi.nlm.nih.gov/pubmed/37928929
http://dx.doi.org/10.4102/sajr.v27i1.2729
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