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Kuo, T.T., Chen, T.C., Lee, L.Y. and Lu, P.H. (2009) IgG4-Positive Plasma Cells in Cutaneous Rosai-Dorfman Disease: An Additional Immunohistochemical Feature and Possible Relationship to IgG4-Related Sclerosing Disease. Journal of Cutaneous Pathology, 36, 1069-1073.
https://doi.org/10.1111/j.1600-0560.2008.01222.x

has been cited by the following article:

• TITLE: Recurrent Bilateral Orbital Infiltration as Primary Manifestation of Rosai Dorfman Disease

  AUTHORS: Belinda Pustina, Naser Salihu, Arben Rroji, Gentian Kaloshi, Mentor Petrela

  KEYWORDS: Extranodal Rosai Dorfman, Genetic, Immunodeficiency, Histiocytosis with Massive Lymphadenopathy, Orbit, Kidney

  JOURNAL NAME: Open Journal of Ophthalmology, Vol.7 No.3, August 30, 2017

  ABSTRACT: Rosai Dorfman disease, also known as histiocytosis with massive lymphadenopathy, is a very rare idiopathic disease. It is characterized by over production and accumulation of non Langerhans sinus histiocyte most often in lymph nodes, but may occur in other areas leading to organ damage. Based on the research, it can be caused by an infectious agent, immunodeficiency or autoimmunity and genetic causes. Extranodal manifestation is uncommon, however extranodal sites include liver, kidney, respiratory organs, orbit and eyeball. We present a case report of a 44-year-old female with recurrent bilateral orbital infiltration as first location of Rosai Dorfman disease.