منابع مشابه
Rosai-Dorfman Disease: A Case Report and Literature Review
Rosai-Dorfman disease or sinus histiocytosis with massive lymphadenopathy is a rare disorder that typically manifests as lymphadenopathy and systemic symptoms whose etiology remains poorly elucidated. The diagnosis is based on immunohistochemistry. Its treatment is poorly defined but the prognosis is usually favorable. Here we report a 14 year old boy who presented with massive bilateral cervi...
متن کاملCutaneous Rosai-Dorfman disease: a case report.
A 40-year-old female presented with a 2-year history of asymptomatic nodules on her lower extremity. Symptoms began with a small dark spot on the right thigh, which progressively enlarged. She then developed similar nodules on her right leg and a lesion on her left buttock. On physical exam, her right proximal lateral thigh revealed a 10 cm x 6 cm indurated, pink-brown, heterogeneous plaque wit...
متن کاملRosai Dorfman Disease in a Pregnant Female: a Case Report
Rosai Dorfman disease (RDD) or sinus histiocytosis is a rare, idiopathic, non neoplastic histiocytic proliferation of unknown etiology typically presenting with massive cervical lymphadenopathy with or without systemic involvement. It may occur in any age group, but is most commonly seen in children and young adults. We report a case of RDD with bilateral massive cervical swelling in a 21 years...
متن کاملRosai-Dorfman syndrome: a case report.
A 30-year-old woman presented with multiple swellings in the neck associated with febrile illness of 3 months' duration. She also complained of nasal blockade. The swellings were non-tender, non-matted with about 4-5 cm in size. CT scan of nose and paranasal sinuses revealed a mass in the right nasal cavity. Histopathology from cervical lymph nodes which showed large clusters of mononuclear foa...
متن کاملRosai-Dorfman disease with primary cutaneous manifestations--a case report.
Rosai-Dorfman disease (sinus histiocytosis with massive lymphadenopathy) is a benign systemic proliferative disorder of histiocytes resembling the sinus histiocytes of lymph nodes. The typical clinical features of this disease include bilateral painless lymphadenopathy, fever, and polyclonal hyperglobulinaemia. The condition may present with extranodal involvement in 43% of cases, and cutaneous...
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ژورنال
عنوان ژورنال: Haematology Journal of Bangladesh
سال: 2020
ISSN: 2707-1405,2523-1219
DOI: 10.37545/haematoljbd201943