Print ISSN: 2581-5725
Online ISSN: 2456-9267
CODEN : IACHCL
IP Archives of Cytology and Histopathology Research (ACHR) open access, peer-reviewed quarterly journal publishing since 2016 and is published under the Khyati Education and Research Foundation (KERF), is registered as a non-profit society (under the society registration act, 1860), Government of India with the vision of various accredited vocational courses in healthcare, education, paramedical, yoga, publication, teaching and research activity, with the aim of faster and better dissemination of knowledge, we will be publishing the article more...Case Report
Author Details :
Volume : 2, Issue : 4, Year : 2017
Article Page : 96-99
Abstract
Rosai dorfmann disease (RDD) is a rare disease of histiocytic origin, with an obscure aetiology. Usually it manifests as bilateral cervical lymphadenopathy in young adults, with cutaneous involvement seen in 43% cases. Pure cutaneous from of RDD (PC - RDD) is very rare and amount for 3% of RDD. PC- RDD is enigmatic for the clinicians as the diagnosis is often delayed or missed due to its rarity, vague and overlapping presentations. We here in report a PC – RDD in a 53 year old male with a brief review of literature.
Keywords: Cutaneous, Rosai Dorfmann, Emperipolesis.
How to cite : Amita K, Shankar V, Singh A, Sarvesh, Pure Cutaneous form of Rosai Dorfmann disease- A cute surprise in the cutis. IP Arch Cytol Histopathol Res 2017;2(4):96-99
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