Sinus Histocytosis with Splenomegaly in Children- A Rare Case Report

Kuntal Roy, Fabia Hannan Mone, Syed Khairul Amin, Md. Ekhlasur Rahman and Soma Halder 2019. Sinus Histocytosis with Splenomegaly in Children- A Rare Case Report. Anwer Khan Modern Medical College Journal. 10 (2), pp. 176-178. https://doi.org/10.3329/akmmcj.v10i2.44132

TitleSinus Histocytosis with Splenomegaly in Children- A Rare Case Report
TypeJournal article
AuthorsKuntal Roy, Fabia Hannan Mone, Syed Khairul Amin, Md. Ekhlasur Rahman and Soma Halder
Abstract

Sinus Histiocytosis/Rosai-Dorfman Disease (RDD) are benign, rare proliferative disorder caused by over production and accumulation of specific type of white blood cell (Phagocytic Histiocyte) in the lymph nodes of the body. Here, lymphadenopathy mostly painless and commonly found in the neck (cervical) but  may occur in other areas of the body such as skin, lung, central nervous system, kidney (less than 5%). Predominantly it affects the young age group of children, adolescents or young adults. In spite of spontaneous remissions, treatment strategies can be different according to involvement and severity (RDD-  Seldom life threatening disease).

JournalAnwer Khan Modern Medical College Journal
Journal citation10 (2), pp. 176-178
ISSN2304-5701
2221-836X
Year2019
PublisherAnwer Khan Modern Medical College & Hospital
Digital Object Identifier (DOI)https://doi.org/10.3329/akmmcj.v10i2.44132
Web address (URL)https://www.banglajol.info/index.php/AKMMCJ/article/view/44132
Publication dates
Published20 Nov 2019

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