Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature

Rosai–Dorfman disease (RDD) predominantly affects cervical lymph nodes and presents with fever and pancytopenia. Central nervous system involvement though uncommon is often reported. Hydrocephalus and paraparesis as a consequence of RDD is an extremely rare entity. We present a 58-year-old male, dia...

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Autores principales: Kapoor, Ankur, Salunke, Pravin, Ahuja, Chirag K., Chatterjee, Debjyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898121/
https://www.ncbi.nlm.nih.gov/pubmed/29682050
http://dx.doi.org/10.4103/ajns.AJNS_30_16
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author Kapoor, Ankur
Salunke, Pravin
Ahuja, Chirag K.
Chatterjee, Debjyoti
author_facet Kapoor, Ankur
Salunke, Pravin
Ahuja, Chirag K.
Chatterjee, Debjyoti
author_sort Kapoor, Ankur
collection PubMed
description Rosai–Dorfman disease (RDD) predominantly affects cervical lymph nodes and presents with fever and pancytopenia. Central nervous system involvement though uncommon is often reported. Hydrocephalus and paraparesis as a consequence of RDD is an extremely rare entity. We present a 58-year-old male, diagnosed and treated for RDD with cervical lymphadenopathy, who now presented with spastic paraparesis and on evaluation was found to have communicating hydrocephalus that resolved after ventriculoperitoneal shunt surgery.
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spelling pubmed-58981212018-04-20 Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature Kapoor, Ankur Salunke, Pravin Ahuja, Chirag K. Chatterjee, Debjyoti Asian J Neurosurg Case Report Rosai–Dorfman disease (RDD) predominantly affects cervical lymph nodes and presents with fever and pancytopenia. Central nervous system involvement though uncommon is often reported. Hydrocephalus and paraparesis as a consequence of RDD is an extremely rare entity. We present a 58-year-old male, diagnosed and treated for RDD with cervical lymphadenopathy, who now presented with spastic paraparesis and on evaluation was found to have communicating hydrocephalus that resolved after ventriculoperitoneal shunt surgery. Medknow Publications & Media Pvt Ltd 2018 /pmc/articles/PMC5898121/ /pubmed/29682050 http://dx.doi.org/10.4103/ajns.AJNS_30_16 Text en Copyright: © 2018 Asian Journal of Neurosurgery 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
Kapoor, Ankur
Salunke, Pravin
Ahuja, Chirag K.
Chatterjee, Debjyoti
Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title_full Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title_fullStr Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title_full_unstemmed Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title_short Spastic Quadriparesis and Communicating Hydrocephalus as Late Sequel of Rosai–Dorfman Disease: A Case Report and Review of Literature
title_sort spastic quadriparesis and communicating hydrocephalus as late sequel of rosai–dorfman disease: a case report and review of literature
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898121/
https://www.ncbi.nlm.nih.gov/pubmed/29682050
http://dx.doi.org/10.4103/ajns.AJNS_30_16
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