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Rosai–Dorfman disease with isolated lacrimal gland enlargement

Rosai–Dorfman Disease also called as Sinus Histiocytosis with Massive Lymphadenopathy is a rare, benign, idiopathic histiocytic proliferative disorder that occurs predominantly in children and young adults. Orbital involvement can occur in 11% of cases. Isolated lacrimal gland involvement without an...

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Autores principales: Pauly, Marian, Naik, Mekhla, Subramanian, Krishnakumar, Anantharaman, Giridhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219316/
https://www.ncbi.nlm.nih.gov/pubmed/30505130
http://dx.doi.org/10.4103/ojo.OJO_110_2016
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author Pauly, Marian
Naik, Mekhla
Subramanian, Krishnakumar
Anantharaman, Giridhar
author_facet Pauly, Marian
Naik, Mekhla
Subramanian, Krishnakumar
Anantharaman, Giridhar
author_sort Pauly, Marian
collection PubMed
description Rosai–Dorfman Disease also called as Sinus Histiocytosis with Massive Lymphadenopathy is a rare, benign, idiopathic histiocytic proliferative disorder that occurs predominantly in children and young adults. Orbital involvement can occur in 11% of cases. Isolated lacrimal gland involvement without any local or systemic recurrence is very rare. To the best of our knowledge, only seven cases have been reported in the literature till date. Histopathological and immunohistochemical confirmation is essential in establishing the diagnosis. A benign course is usual, but in some cases, blindness or even fatality may result. We report a case of 30-year-old female with isolated lacrimal gland involvement and 19 months' follow-up.
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spelling pubmed-62193162018-11-30 Rosai–Dorfman disease with isolated lacrimal gland enlargement Pauly, Marian Naik, Mekhla Subramanian, Krishnakumar Anantharaman, Giridhar Oman J Ophthalmol Case Report Rosai–Dorfman Disease also called as Sinus Histiocytosis with Massive Lymphadenopathy is a rare, benign, idiopathic histiocytic proliferative disorder that occurs predominantly in children and young adults. Orbital involvement can occur in 11% of cases. Isolated lacrimal gland involvement without any local or systemic recurrence is very rare. To the best of our knowledge, only seven cases have been reported in the literature till date. Histopathological and immunohistochemical confirmation is essential in establishing the diagnosis. A benign course is usual, but in some cases, blindness or even fatality may result. We report a case of 30-year-old female with isolated lacrimal gland involvement and 19 months' follow-up. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC6219316/ /pubmed/30505130 http://dx.doi.org/10.4103/ojo.OJO_110_2016 Text en Copyright: © 2018 Oman Ophthalmic Society http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Case Report
Pauly, Marian
Naik, Mekhla
Subramanian, Krishnakumar
Anantharaman, Giridhar
Rosai–Dorfman disease with isolated lacrimal gland enlargement
title Rosai–Dorfman disease with isolated lacrimal gland enlargement
title_full Rosai–Dorfman disease with isolated lacrimal gland enlargement
title_fullStr Rosai–Dorfman disease with isolated lacrimal gland enlargement
title_full_unstemmed Rosai–Dorfman disease with isolated lacrimal gland enlargement
title_short Rosai–Dorfman disease with isolated lacrimal gland enlargement
title_sort rosai–dorfman disease with isolated lacrimal gland enlargement
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6219316/
https://www.ncbi.nlm.nih.gov/pubmed/30505130
http://dx.doi.org/10.4103/ojo.OJO_110_2016
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