Results 21 to 30 of about 6,609 (224)
Doença de Rosai-Dorfman cutânea Cutaneous Rosai-Dorfman Disease
Doença de Rosai-Dorfman é uma doença benigna e autolimitada. Tem etiologia desconhecida e foi descrita pela primeira vez por Rosai e Dorfman em 1969. As manifestações clássicas incluem linfadenopatia cervical usualmente acompanhada por febre, leucocitose
Fábio Machado Landim+5 more
doaj +1 more source
Orbital involvement in Rosai-Dorfman disease [PDF]
A doença de Rosai-Dorfman (DRD) ou histiocitose sinusal com linfadenopatia maciça é uma entidade clínica idiopática, rara e benigna, caracterizada pela proliferação histiocitária com linfofagocitose. Geralmente se apresenta com linfoadenomegalia cervical,
GONÇALVES, Allan C. Pieroni+4 more
core +2 more sources
Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment
Rosai‐Dorfman disease is referred to as sinus histiocytosis massive lymphadenopathy. We are reporting a rare case of Rosai‐Dorfman disease, a case of 6‐year‐old boy with a history of multiple painless submandibular and cervical lymphadenopathy.
Kalpana Giri+3 more
doaj +1 more source
Potential role of 18F-FDG PET/CT in a case of progressive Rosai Dorfman disease [PDF]
Rosai Dorfman disease is a rare form of nonlangerhans cell histiocytosis, presenting with extensive lymphadenopathies. Treatment in most cases of nodal disease, involves close observation; however, extranodal involvement requires a more definitive ...
Armaghan Fard-Esfahani+4 more
doaj +1 more source
Sinus Histiocytosis: An Uncommon Presentation of an Uncommon Condition [PDF]
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
Rosai-Dorfman disease mimicking gastrointestinal tuberculosis and fungal sinusitis: A case report
Every organ can be affected by Rosai-Dorfman disease, the most common being skin and soft tissue, bone and upper respiratory tract. Here we present a Rosai-Dorfman disease patient who manifested with multiple organ involvement.
Seid Getahun Abdela, MD+1 more
doaj
Rosai-Dorfman disease is a rare, usually benign, entity that mostly affects children and adolescents. We report a clinical case in which the most common clinical and imaging manifestation is present: cervical lymphadenopathy. Histological confirmation is
Carvalho, André+5 more
core +2 more sources
Extranodal rosai dorfman disease: a case report of single soft tissue cystic lesion [PDF]
Rosai-Dorfman disease (RDD) is an uncommon benign histiocytic disorder. It is found worldwide and slightly more common among in men (1.4:1), affecting individuals are with an average age of 20.6 years. Extranodal tissue involvement is documented in 25-43%
Agrawal, Ruchi+2 more
core +2 more sources
Rosai Dorfman disease- A rare entity: Case report in North Indian male
Rosai Dorfman disease is a rare disease characterized by histiocytic proliferation of lymph node in young adults. We present here the case of a 67 years old Indian male presenting with lymphadenopathy and pyrexia of unknown origin for 16 months duration.
Ankur Baruah
doaj +1 more source
Le syndrome de rosai dorfman de l’enfant (a propos d’un cas) [PDF]
Le syndrome de rOSaï DOrFman ou histiocytose sinusale avec lymphadénopathie massive est une maladie rare d’étiologie inconnue, peut se voir à tout âge, l’enfant n’étant pas épargné.
Belaabida, B+4 more
core +2 more sources