Results 21 to 30 of about 5,266 (225)
Case Reports in Radiology, 2018 Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder.
Rashid AL Umairi +4 more
doaj +1 more source
Lung India, 2020 Rosai–Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign disease that usually presents as massive and painless cervical lymphadenopathy.
Ambika Sharma +5 more
doaj +1 more source
Erdheim-Chester Disease: a comprehensive review of the literature [PDF]
, 2013 Erdheim-Chester Disease (ECD) is a rare form of non Langerhans' cell histiocytosis. Individuals affected by this disease are typically adults between their 5th and 7th decades of life. Males and females are almost equally affected.
Mirra Manevich-Mazor +2 more
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A Rare Case of Multiorgan Involvement of Rosai Dorfman Disease in an Elderly Female
Journal of Nepal Medical Association, 2014 Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, most frequently seen in children and young adults.The disease is more common in males and in individuals ...
Rakesh Digambar Waghmare
doaj +1 more source
Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]
, 2015 Introduction Rosai–Dorfman Disease (RDD), also known as Sinus Histiocytosis with Massive Lymphadenopathy (SHML), is a rare, benign, proliferative disorder of macrophages and monocytes that was first described by Rosai and Dorfman in 1969.
Greco, MD, Allison, Kane, MD, Gregory
core +2 more sources
Histocytopathological diagnosis of Rosai–Dorfman disease: Case report
Clinical Case Reports, 2022 Sinus histiocytosis with massive lymphadenopathy (Rosai–Dorfman disease) being a rare benign proliferative self‐limiting disease of the cells of macrophage‐histiocyte family is of unknown etiology and presents with massive lymphadenopathy.
Zephania Saitabau Abraham +4 more
doaj +1 more source
A rare case of oral multisystem Langerhans cell histiocytosis [PDF]
, 2017 Langerhans cell histiocytosis (LCH) is a rare disorder characterized by high proliferation of Langerhans dendritic cells. LCH is a solitary or multifocal disease that primarily involves bone tissue and often affects children and young men. A 29 years-old
Facciolo, Maria Teresa +4 more
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Differential Diagnoses of Systemic Mastocytosis in Routinely Processed Bone Marrow Biopsy Specimens: A Review [PDF]
, 2010 Diagnosis of systemic mastocytosis (SM) is mainly based on the morphological demonstration of compact mast cell infiltrates in various tissue sites. In almost all patients such infiltrates are detected in the bone marrow.
Horny, H. -P., Sotlar, K., Valent, P.
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Langerhan’s cell Histiocytosis of Sphenoid Sinus causing Vision Loss: A Case Report
Journal of Nepal Medical Association, 2019 Langerhan's cell histiocytosis is an uncontrolled proliferation of dendritic cells. The involvement of skull base is rare. Variable clinical presentation and multi organ involvement often warrant a multidisciplinary approach for a successful diagnosis ...
Suresh Mani +3 more
doaj +1 more source
Unusual presentation of Rosai-Dorfman disease in a 14-month-old Italian child: a case report and review of the literature [PDF]
, 2016 Background: Rosai-Dorfman disease (RDD) is a rare form of histiocytosis characterized by histiocyte proliferation within lymph nodes and extranodal tissue. Here we report an unusual presentation of RDD in an Italian toddler.
Bruzzi, Patrizia +5 more
core +2 more sources