Rosai–Dorfman disease: cutaneous form
Клинический разбор в общей медицинеThe proliferative disease of histiocytes presented in the article is rarely encountered in the practice of a dermatovenerologist. Rosai-Dorfman disease is a benign disease of unclear etiology, which may be accompanied by extensive lymphadenopathy of the ...
Nadezhda V. Krasnova +6 more
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Rosai - Dorfman disease: a rare entity diagnosed at autopsy
Autopsy and Case Reports, 2013 Rosai-Dorfman disease (RDD) or Sinus histiocytosis with massive lymphadenopathy is a rare and benign histiocytic proliferative disorder first described by Juan Rosai and Ronald Dorfman in 1969, whose etiology remains unknown.
João da Costa Veloso Neto +2 more
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Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]
, 2018 The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana +3 more
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A Case Report Diagnosed with Rosai-Dorfman Disease by Voice Change [PDF]
, 2014 Rosai-Dorfman disease is a rare disorder of unknown of etiology and is usually associated with benign proliferation of hematopoietic and fibrous tissue that often manifest in the head and neck region.
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Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital [PDF]
, 2011 Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
Adeyemo, W. L. +4 more
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BRAF V600E mutation detected in a case of Rosai-Dorfman disease
Haematologica, 2018 Rosai-Dorfman Disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare, nonmalignant histiocytic proliferation of unknown etiology. According to the new classification, it belongs to the R group of histiocytoses.[1][1] The
G. Fatobene +8 more
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Extra Nodal (Cutaneous) Rosai Dorfman Disease
Online Journal of Health & Allied Sciences, 2020 Rosai-Dorfman disease is an extremely rare disorder characterized by proliferation and accumulation of histiocytes in lymph nodes, usually in the cervical region. In approximately 43% cases, this accumulation occurs in extra nodal sites such as the skin,
Talha Ahmed +5 more
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A Case of Refractory Langerhans Cell Histiocytosis Complicated with Hemophagocytic Lymphohistiocytosis Rescued by Cord Blood Transplantation with Reduced-intensity Conditioning [PDF]
, 2017 We diagnosed a female infant with Langerhans cell histiocytosis (LCH) who was refractory to conventional chemotherapy. She showed refractory inflammation that was complicated with hemophagocytic lymphohistiocytosis (HLH) during LCH chemotherapy ...
Kanamitsu, Kiichiro +4 more
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Rosai–Dorfman disease as chronic bilateral granulomatous anterior uveitis: A case report
SAGE Open Medical Case ReportsRosai–Dorfman disease is a rare non-Langerhans cell histiocytosis disorder, also known as sinus histiocytosis, with massive lymphadenopathy. Rosai–Dorfman disease is classified into nodal and extranodal diseases.
Yaninsiri Ngathaweesuk +1 more
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Cutaneous Rosai-Dorfman disease: A separate clinical entity
Journal of Dermatology and Dermatologic Surgery, 2017 Rosai-Dorfman disease is a benign, self-limited non-Langerhans cell histiocytosis of unknown etiology. Its most common clinical feature is extraordinary massive painless cervical lymphadenopathy.
Tiffany Hinojosa +6 more
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