Results 91 to 100 of about 289,368 (261)
Aggressive Neoplasms That Mimic Chronic Endodontic Lesions: A Multi‐Institutional Case Series
Australian Endodontic Journal, Volume 51, Issue 2, Page 415-422, August 2025.ABSTRACT This study aimed to report sociodemographic, clinicopathologic and radiological features of 12 cases of aggressive neoplasms that were clinically diagnosed as chronic endodontic lesions. The series comprised seven females (58.33%) and five males (41.67%), with a mean age of 48.9 ± 19.19 years (range: 16–75 years).
Natália Gonçalves Macedo +11 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
Toxoplasma IgG Expressed in a Patient With Rosai-Dorfman Disease
Kaohsiung Journal of Medical Sciences, 2010 Rosai-Dorfman Disease (RDD) is a rare benign disease characterized by sinus histiocytosis with massive lymphadenopathy. RDD can be differentiated from other types of histiocytosis by immunochemical analysis, as RDD is positive for S100.
Hung-Ju Liao, Ching-Wen Chiang
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
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
, 2012 Melanoma is a relatively common neoplasm which is increasing in incidence. Melanoma appears as a variegated irregular maculopapular lesion usually on the skin, but possibly on mucosae, conjunctiva, orbit, nails and oesophagus. They may be black, brown,
Magri, Stephanie, Pace, Keith
core +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
Florid dermatopathic lymphadenopathy—A morphological mimic of Langerhans cell histiocytosis
Clinical Case Reports, 2018 Key Clinical Message The histopathology of reactive florid dermatopathic lymphadenopathy shows overlap with Langerhans cell histiocytosis (LCH) involving the lymph node, which may lead to misdiagnosis.
Aishwarya Ravindran +4 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 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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