Rosai – Dorfman disease is a disorder of histiocytic proliferation that can affect almost every organ. Skin may be involved in about 10% cases, but only 3% of patients have skin lesions exclusively. Patients with CRDD usually are healthy, without leading constitutional or other symptoms. Etiology of this disease is unclear, but it might be triggered by an infectious agent such as Herpesvirus 6 and Epstein-Barr virus, there is also predisposition to autoimmune diseases, hematological malignancies. In our case patient was diagnosed with Borrelia burgdorferi infection. Any known association between this infection and Rosai – Dorfman disease was not described before. The disease may manifest in any age group. The differential diagnosis includes...
A 52‐year‐old woman developed progressive infiltrated purple and hyperpigmented cutaneous lesions in...
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descri...
Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by mas...
Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limite...
Rosai-Dorfman disease (RDD) is a rare benign proliferative disorder of histiocytes in the lymph node...
Cutaneous Rosai-Dorfman disease (CRDD) is a rare proliferative disorder of histiocytes with unknown ...
Background:Rosai-Dorfman also known as sinus histiocytosis with massive lymphadenopathy is a benig...
Rosai-Dorfman disease (RDD) of sinus histiocytosis with massive lymphadenopathy (SHML) is a benign, ...
Rosai-Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a benign p...
Rosai-Dorfman disease (RDD) is a nonmalignant histiocytic disorder of unknown origin that is extreme...
Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is a benign systemic prolif...
Abstract: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. ...
Rosai-Dorfman disease rarely presents in a solely cutaneous form. A subset of patients with skin lim...
Rosai-Dorfman disease (RDD) is a rare histiocytic condition of unknown etiology. Patients with RDD c...
Rosai–Dorfman disease (RDD) is a rare disorder characterized by the proliferation of his...
A 52‐year‐old woman developed progressive infiltrated purple and hyperpigmented cutaneous lesions in...
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descri...
Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by mas...
Cutaneous Rosai-Dorfman disease is a rare, lymphoproliferative disease. It is benign and self-limite...
Rosai-Dorfman disease (RDD) is a rare benign proliferative disorder of histiocytes in the lymph node...
Cutaneous Rosai-Dorfman disease (CRDD) is a rare proliferative disorder of histiocytes with unknown ...
Background:Rosai-Dorfman also known as sinus histiocytosis with massive lymphadenopathy is a benig...
Rosai-Dorfman disease (RDD) of sinus histiocytosis with massive lymphadenopathy (SHML) is a benign, ...
Rosai-Dorfman disease, also known as sinus histiocytosis with massive lymphadenopathy, is a benign p...
Rosai-Dorfman disease (RDD) is a nonmalignant histiocytic disorder of unknown origin that is extreme...
Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is a benign systemic prolif...
Abstract: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. ...
Rosai-Dorfman disease rarely presents in a solely cutaneous form. A subset of patients with skin lim...
Rosai-Dorfman disease (RDD) is a rare histiocytic condition of unknown etiology. Patients with RDD c...
Rosai–Dorfman disease (RDD) is a rare disorder characterized by the proliferation of his...
A 52‐year‐old woman developed progressive infiltrated purple and hyperpigmented cutaneous lesions in...
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descri...
Rosai-Dorfman disease (RDD) is a rare benign proliferative histiocytic disorder characterised by mas...