Results 91 to 100 of about 286,204 (263)
Rosacea in childhood and adolescence: A review
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 6, Page 684-691, June 2025.Summary Despite presenting with similar symptoms, triggers, and progression patterns as adults, rosacea in children and adolescents is frequently overlooked as a primary differential diagnosis. However, initial manifestations of classic clinical types can be observed from infancy onwards.
Sören Korsing +4 more
wiley +1 more source
Rosai and Dorfman Disease with Pleural Involvement: Case Report
The Scientific World Journal, 2008 Sinus histiocytosis with massive lymphadenopathy (SHLM) disease is considered to be an indolent and self-limiting pathology. However, severe morbidity and mortality have been attributed to complications of SHLM.
Jouda Cherif +5 more
doaj +1 more source
Management of a patient with Rosai–Dorfman syndrome and large adrenal pheochromocytoma
Iraqi Journal of Hematology, 2018 Sinus histiocytosis with massive lymphadenopathy that known as Rosai Dorfman syndrome (RDS)is a rare histiocytic disease which includes benign lymph nodes (LN) enlargement with extra-lymphatic soft tissue involvement.
Taha O Mahwi, Najmaddin Khoshnaw
doaj +1 more source
Journal of Gastrointestinal Cancer, 2012 Sinus histiocytosis with massive lymphadenopathy (SHML) was first described in 1969 by Rosai and Dorfman [1]. It is a rare inflammatory disorder with key clinicopathological characteristics such as emperipolesis and positive immunostaining for S-100 ...
Minerva A. Romero Arenas +3 more
semanticscholar +1 more source
Immunoglobulin G4–Related Disease of the Sternoclavicular Joint: A Case Report
Clinical Case Reports, Volume 13, Issue 4, April 2025.ABSTRACT This case highlights the possibility that Immunoglobulin G4‐related disease (IgG4‐RD) lesions can also occur in the sternoclavicular joint. If a neoplastic lesion is found in the sternoclavicular joint, a biopsy should be attempted to diagnose IgG4‐RD as a differential.
Remi Mizuta +18 more
wiley +1 more source
Serum anti-Müllerian hormone concentrations before and after treatment of an ovarian granulosa cell tumour in a cat [PDF]
, 2017 Case summary A 15-year-old female cat was presented for investigation of progressive behavioural changes, polyuria, polydipsia and periuria. An ovarian granulosa cell tumour was identified and the cat underwent therapeutic ovariohysterectomy (OHE).
Fowkes, R C +8 more
core +2 more sources
Journal of Health Science and Medical Research (JHSMR), 2003 Sinus histiocytosis with massive lymphadenopathy (SHML) or Rosai-Dorfman disease is an unusual, benign, selflimited condition of unknown etiology which generally presents as massive bilateral cervical lymphadenopathy in children.
R Tangsathitporn, A Nitiruangjarus
doaj
CytoJournal, 2011 Rosai–Dorfman disease (RDD), a rare, benign, self-limiting histiocytic proliferative disorder, can be encountered in both nodal and extranodal locations, and fine needle aspiration (FNA), a simple, accurate and economic tool, has been widely used for the
Yuquan Shi +4 more
semanticscholar +1 more source
Journal of Small Animal Practice, Volume 66, Issue 4, Page 272-279, April 2025.Objectives To describe thoracic and abdominal imaging findings in dogs with immune‐mediated polyarthritis and to evaluate their impact on the decision to commence immunosuppressive therapy. Materials and Methods Retrospective case series describing imaging findings in dogs with immune‐mediated polyarthritis across modalities, including thoracic ...
L. Atkinson +4 more
wiley +1 more source
Journal of Cytology, 2009 Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi +2 more
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