ROSAI-DORFMAN DISEASE: REPORT OF A RARE CASE OF PERIPHERAL LYMPHADENOPATHY.

2019 ◽  
Vol 13 (01) ◽  
pp. 1-5
Author(s):  
Farouk AG ◽  
◽  
Zarami AB ◽  
Ahmadu MS ◽  
Ambe JP ◽  
...  
Keyword(s):  
Rare Case ◽  
Rosai Dorfman Disease

scholarly journals A rare case of Rosai–Dorfman disease presenting with cardiac tamponade

2019 ◽  
Vol 20 (6) ◽  
pp. 718-718
Author(s):  
Jason M Tarkin ◽  
Virginia Wolstenholme ◽  
Michael Sheaff ◽  
Mark Westwood ◽  
Charlotte Manisty
Keyword(s):  
Cardiac Tamponade ◽  
Rare Case ◽  
Rosai Dorfman Disease

scholarly journals Unusual Presentation of Rosai-Dorfman Disease: Report of a Rare Case

2019 ◽  
Vol 20 ◽  
pp. 91-96
Author(s):  
Khalid Waleed AlKuwaity ◽  
Meshal Hamoud Alosaimi ◽  
Khallad Tariq Alsahlawi ◽  
Mohammed Abdullatif Alomair ◽  
Mohammad Abdullah Battyour ◽  
...  
Keyword(s):  
Rare Case ◽  
Unusual Presentation ◽  
Rosai Dorfman Disease

A rare case of extranodal Rosai-Dorfman disease

2006 ◽  
Vol 79 (946) ◽  
pp. e117-e119 ◽  
Author(s):  
D Chopra ◽  
W E Svensson ◽  
P Forouhi ◽  
S Poole
Keyword(s):  
Rare Case ◽  
Rosai Dorfman Disease

Spinal Rosai-Dorfman Disease: A Rare Case Report

2014 ◽  
Vol 1 (4) ◽  
pp. 158-160
Author(s):  
S Syed Ali ◽  
Shailendra Markad Uttamrao
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rosai Dorfman Disease ◽  
Rare Case Report

scholarly journals Rosai Dorfman Disease

2021 ◽  
Author(s):  
Kalpana Giri ◽  
Ashok Baral ◽  
Niva Tiwari ◽  
Krishna Sharma
Keyword(s):  
Rare Case ◽  
Cervical Lymphadenopathy ◽  
Unknown Origin ◽  
Sinus Histiocytosis ◽  
Massive Lymphadenopathy ◽  
Rosai Dorfman Disease ◽  
History Of

Rosai-Dorfman disease (RDD) is referred to as Sinus Histiocytosis Massive Lymphadenopathy (SHML) of unknown origin. We are reporting a rare case of Rosai Dorfman disease, a case of 6 years old male with a history of multiple painless bilateral submandibular and cervical lymphadenopathy.

scholarly journals Sinus Histocytosis with Splenomegaly in Children- A Rare Case Report

2019 ◽  
Vol 10 (2) ◽  
pp. 176-178
Author(s):  
Kuntal Roy ◽  
Fabia Hannan Mone ◽  
Syed Khairul Amin ◽  
Md Ekhlasur Rahman ◽  
Soma Halder
Keyword(s):  
Central Nervous System ◽  
Nervous System ◽  
Rare Case ◽  
Treatment Strategies ◽  
The Body ◽  
Age Group ◽  
Medical College ◽  
Rosai Dorfman Disease ◽  
Rare Case Report ◽  
Life Threatening

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). Anwer Khan Modern Medical College Journal Vol. 10, No. 2: July 2019, P 176-178

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