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Juan, 20th-century U.S. pathologist. See: Rosai-Dorfman disease.
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References in periodicals archive ?
Treatment of sinus histiocytosis with massive lymphadenopathy (rosai?dorfman disease): Report of a case and literature review.
(2) Department of Pathology, Osaka Rosai Hospital, 1179-3 Nagasone, Kitaku, Sakai, Osaka 591-8025, Japan
Rosai, "The digestive system manifestations of Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy): Review of 11 cases," Human Pathology, vol.
Identification of emperipolesis within the histiocyte cytoplasm is pathognomonic as originally described by Rosai et al., though histiocytes are less common in extranodal tissue [1-7, 15].
Both show a variable degree of fibrosis and spare skin adnexal structures.9,10 Later Rosai et al11 delineated ALHE better.
The term RDD was first introduced into scientific literature in 1969 when Juan Rosai and Ronald Dorfman described four cases of a rare, idiopathic, non-neoplastic lymphoproliferative disorder.
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign source of lymphadenopathy of unknown aetiology, first described in 1969 by Rosai and Dorfman (cited by Moore et al.
Rosai, "Mediastinum," in Rosai and Ackerman's Surgical Pathology, J.
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a clinico-pathological entity described by Rosai and Dorfman (1) just over 40 years ago.
Desmoplastic small round cell tumor (DSRCT) is an extremely rare, highly aggressive, and malignant neoplasm initially reported by Gerald and Rosai in 1989 [1].