Results 81 to 90 of about 5,266 (225)
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Wegener's granulomatosis (WG) could be a lethal disease if not diagnosed and managed timely. Oral involvement is rare and often presents as gingival hyperplasia with a traditional “strawberry gingivitis” appearance. Dental practitioners may be the first ones to encounter WG and may be able to prevent disease progression like the present case ...
Samaneh Salari +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
Primary oral manifestation of Langerhans cell histiocytosis refractory to conventional therapy but susceptible to BRAF-specific treatment: a case report and review of the literature [PDF]
, 2019 Langerhans cell histiocytosis (LCH) is a diagnostic and therapeutic challenge. We report on a rare case of its primary oral manifestation that was treated successfully with the BRAF-specific agent, vemurafenib, after insufficient standard LCH treatment ...
Beck-Broichsitter, Benedicta +8 more
core +1 more source
Pediatric Allergy and Immunology, Volume 37, Issue 1, January 2026.
Clément Triaille +2 more
wiley +1 more source
Clinical Case Reports, Volume 13, Issue 10, October 2025.ABSTRACT Diagnosis of Kimura's disease should be considered if a middle‐aged Asian male patient presents with painless enlargement of cervical lymph nodes, eosinophilia, and elevated serum total IgE level. Patients with Kimura's disease can have concurrent EGPA or presentations consistent with EGPA.
Wei Du +3 more
wiley +1 more source
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
EPSTEIN-BARR-VIRUS ASSOCIATED SYNDROMES IN IMMUNOSUPPRESSED LIVER-TRANSPLANT RECIPIENTS - CLINICAL PROFILE AND RECOGNITION ON ROUTINE ALLOGRAFT BIOPSY [PDF]
, 1990 The clinical profile and histopathologic changes in needle biopsies of the liver were studied in 10 cases of acute Epstein-Barr virus infection occurring in liver transplant recipients.
DEMETRIS, AJ +3 more
core +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
doaj
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