Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis

Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare. Specifically, cardiac involvement in Rosai-Dorfman diseas...

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Autores principales: Sendrasoa, Fandresena Arilala, Ranaivo, Irina Mamisoa, Raharolahy, Onivola, Andrianarison, Malalaniaina, Razanakoto, Naina Harinjara, Ramarozatovo, Lala Soavina, Rapelanoro Rabenja, Fahafahantsoa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107849/
https://www.ncbi.nlm.nih.gov/pubmed/27872644
http://dx.doi.org/10.1155/2016/3920516
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author Sendrasoa, Fandresena Arilala
Ranaivo, Irina Mamisoa
Raharolahy, Onivola
Andrianarison, Malalaniaina
Razanakoto, Naina Harinjara
Ramarozatovo, Lala Soavina
Rapelanoro Rabenja, Fahafahantsoa
author_facet Sendrasoa, Fandresena Arilala
Ranaivo, Irina Mamisoa
Raharolahy, Onivola
Andrianarison, Malalaniaina
Razanakoto, Naina Harinjara
Ramarozatovo, Lala Soavina
Rapelanoro Rabenja, Fahafahantsoa
author_sort Sendrasoa, Fandresena Arilala
collection PubMed
description Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare. Specifically, cardiac involvement in Rosai-Dorfman disease is an extraordinarily infrequent event. We describe a case of a 36-year-old female who presented Rosai-Dorfman disease of multiple organs including the heart, with poor prognosis.
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spelling pubmed-51078492016-11-21 Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis Sendrasoa, Fandresena Arilala Ranaivo, Irina Mamisoa Raharolahy, Onivola Andrianarison, Malalaniaina Razanakoto, Naina Harinjara Ramarozatovo, Lala Soavina Rapelanoro Rabenja, Fahafahantsoa Case Rep Med Case Report Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare. Specifically, cardiac involvement in Rosai-Dorfman disease is an extraordinarily infrequent event. We describe a case of a 36-year-old female who presented Rosai-Dorfman disease of multiple organs including the heart, with poor prognosis. Hindawi Publishing Corporation 2016 2016-10-31 /pmc/articles/PMC5107849/ /pubmed/27872644 http://dx.doi.org/10.1155/2016/3920516 Text en Copyright © 2016 Fandresena Arilala Sendrasoa et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Sendrasoa, Fandresena Arilala
Ranaivo, Irina Mamisoa
Raharolahy, Onivola
Andrianarison, Malalaniaina
Razanakoto, Naina Harinjara
Ramarozatovo, Lala Soavina
Rapelanoro Rabenja, Fahafahantsoa
Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title_full Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title_fullStr Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title_full_unstemmed Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title_short Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis
title_sort rosai-dorfman disease involving multiple organs: an unusual case with poor prognosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5107849/
https://www.ncbi.nlm.nih.gov/pubmed/27872644
http://dx.doi.org/10.1155/2016/3920516
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