Results 31 to 40 of about 1,427 (174)

Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature

open access: yesCase Reports in Oncological Medicine, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a disease of histiocytic proliferation with no known pathogenesis.
Joshua Feriante, Richard T. Lee
doaj   +1 more source

Nodal histiocytic disorder in children: report of three cases and review of literature

open access: yesThe Egyptian Journal of Otolaryngology, 2020
Background Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis.
Indumathi Ainer   +3 more
doaj   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

open access: yesJournal of Cytology, 2011
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala   +2 more
doaj   +1 more source

The Rosai Dorfman Syndrome–The Report of A Rare Case [PDF]

open access: yesJournal of Clinical and Diagnostic Research, 2013
Rosai Dorfman syndrome known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is an uncommon benign systemic histio-proliferative disease which affects lymph nodes, most often those of the neck (cervical lymphadenopathy). The characteristic
Snehalatha R   +3 more
doaj   +1 more source

Rosai Dorfman Disease —A rare case of cervical lymphadenopathy

open access: yesClinical Case Reports, 2020
Rosai Dorfman disease is a rare cause of sinus histiocytosis with massive lymphadenopathy. In developing countries, it often mimics some infectious diseases and malignancies and is often mismanaged.
Insiyah Amiji   +7 more
doaj   +1 more source

Rosai-Dorfman Disease- A Surprise diagnosis in Follow up of SCC Pyriform Sinus -Post Surgery and CTRT [PDF]

open access: yesNational Journal of Laboratory Medicine, 2013
Rosai-Dorfman disease also known as Sinus Histiocytosis with massive Lymphadenopathy (SHML). SHML was first described by Rosai and Dorfman in 1969 [1] and is now considered a non malignant inflammatory disorder in which the precise origin of ...
Nandeesh M, Anitha T.K., Santosh R.
doaj   +1 more source

A rare case of extra nodal Rosai-Dorfman disease with isolated multifocal osseous manifestation

open access: yesIndian Journal of Radiology and Imaging, 2015
Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease is a non-neoplastic condition which typically presents as massive, bilateral cervical lymphadenopathy and can involve multiple extranodal organ systems such as skin, eyes ...
Maharshi H Patel   +3 more
doaj   +1 more source

Role of Fine Needle Aspiration in the Diagnosis of the Rare Disease of Langerhans Cell Histiocytosis in a Child

open access: yesCase Reports in Pathology, 2014
Langerhan’s cell histiocytosis (LCH) results from the proliferation of immunophenotypically and functionally immature, morphologically rounded Langerhan’s cells along with eosinophils, macrophages, lymphocytes, and, commonly, multinucleated giant cells ...
Seema Lale   +2 more
doaj   +1 more source

Primary Rosai-Dorfman Disease of Bone: A Report of Two Cases

open access: yesCase Reports in Radiology, 2019
Rosai-Dorfman disease (RDD), sometimes known as sinus histiocytosis with massive lymphadenopathy, is a rare histiocytic disorder that most commonly presents as painless, massive cervical lymphadenopathy in young adults. Extranodal disease can occur in up
Andrew B. Ross   +3 more
doaj   +1 more source

A report of Rosai–Dorfman disease with systemic multiple lymphadenopathy and high IgG4 plasma cell infiltration

open access: yesSAGE Open Medical Case Reports, 2023
The Rosai-Dorfman disease (RDD) is a kind of sinus histiocytosis with massive lymphadenopathy and is remarkably rare. RDD is characterized by large histiocytes with emperipolesis.
Pingdan Liu   +3 more
doaj   +1 more source

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