Results 11 to 20 of about 4,029 (188)

Rosai-Dorfman Disease of the Breast [PDF]

Cureus, 2017
Rosai-Dorfman disease (also known as sinus histiocytosis with massive lymphadenopathy) is a rare benign proliferative disorder of histiocytes that typically involves the lymph nodes and can also involve extranodal sites. Rosai-Dorfman disease confined to the breast is extremely rare, but important to recognize as it can mimic malignancy. We present the
Delaney, Eileen E., Larkin, Anne C., MacMaster, Sue, Sakhdari, Ali, DeBenedectis, Carolynn M   +4 more
openaire   +6 more sources

Multifocal Rosai Dorfman disease and simultaneous endometrioid ovarian cancer: a case report [PDF]

Journal of Medical Case Reports
Background Rosai Dorfman disease is a rare histiocytosis, which is characterized by accumulation of histiocytes in lymph nodes, but also in extranodal locations. Histologically, one of the key features of Rosai Dorfman disease is emperipolesis. Treatment
Nele Graf, Teresa Halbsguth, Sven Becker, Morva Tahmasbi Rad   +3 more
doaj   +2 more sources

Clinicopathological Features, Treatment Response, and Outcome of Rosai‐Dorfman Disease in Two Children [PDF]

Clinical Case Reports
Rosai‐Dorfman disease is a rare non‐Langerhans cell histiocytic disorder. It is common in male children and young adults of African descent. It is classified into sporadic and familial types.
George Evele, Kouya Francine, Richard Bardin   +2 more
doaj   +2 more sources

Rosai‐Dorfman disease in 6‐year‐old child: Presentation, diagnosis, and treatment

Clinical Case Reports, 2021
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, Ashok Baral, Niva Tiwari, Krishna Sagar Sharma   +3 more
doaj   +2 more sources

Giant intracranial Rosai–Dorfman disease [PDF]

Journal of Clinical Neuroscience, 2004
Rosai-Dorfman disease is a rare, non-neoplastic disease characterized by an unusual proliferation of histiocytic cells. It rarely manifests intracranially, and only 50 cases of intracranial lesions have been reported. We describe an unusual case of a huge, solid mass in the paranasal sinuses, orbits, cavernous sinuses, and suprasellar cisterns.
Ture, U, Seker, A, Bozkurt, SU, Uneri, C, Sav, A, Pamir, MN   +5 more
openaire   +5 more sources

Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis [PDF]

Case Reports in Medicine, 2016
Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare ...
Fandresena Arilala Sendrasoa, Irina Mamisoa Ranaivo, Onivola Raharolahy, Malalaniaina Andrianarison, Naina Harinjara Razanakoto, Lala Soavina Ramarozatovo, Fahafahantsoa Rapelanoro Rabenja   +6 more
doaj   +2 more sources

Spinal Rosai–Dorfman disease: Case report of a rare disorde [PDF]

The Egyptian Journal of Radiology and Nuclear Medicine, 2015
Background: Rosai–Dorfman disease (sinus histiocytosis with massive lymphadenopathy (SHML)) is a rare, histiocytic, lymphoproliferative disease of unknown etiology affecting young people with male predominance.
A. Elsotouhy, M. Abozed, A. Marioud, A. Haider, A. Roux   +4 more
doaj   +2 more sources

Rosai-Dorfman Disease [PDF]

Annals of Plastic Surgery, 2019
Abstract Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign proliferative disease that affects histiocytes. Its etiology remains unclear. Rosai-Dorfman disease primarily affects lymph nodes with many extranodal manifestations present, including cutaneous, pulmonary, ophthalmic ...
Reem, Karami, Fadi, Ghieh, Joe, Baroud, Ghassan, Abu Sittah   +3 more
openaire   +4 more sources

Review and a case of rare Rosai-Dorfman disease [PDF]

Biotechnology & Biotechnological Equipment
Rosai-Dorfman (RDD) is a rare histiocytic syndrome with variable clinical characteristics and extranodal involvement in more than 43% of the patients. This mini-review presents an overview of the literature on Rosai-Dorfman disease.
Dragomira Nikolova, Aleksandar Yordanov, Aleksandra Maslarova, Radka Hristoskova, Vera Damyanova, Savina Hadjidekova, Atanas Radinov   +6 more
doaj   +2 more sources

Orbital and Adnexal Rosai-Dorfman Disease [PDF]

Orbit, 2008
PurposeTo report the clinico-radiological findings, clinical course, and treatment outcomes in five patients with orbital and adnexal Rosai-Dorfman (R-D) disease.MethodsAnalysis of case records of patients with Rosai-Dorfman disease seen at four orbital ...
Venkaṭesh C Prabhakaran, Igal Leibovitch, Raf Ghabrial   +2 more
exaly   +2 more sources