Results 51 to 60 of about 6,609 (224)

Rosai-Dorfman disease manifesting as a solitary mass with fat in the thymus a case report

Journal of Cardiothoracic Surgery
Background Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease, is a rare, self-limiting disease that predominantly affects children and young adults. Moreover, the disease is characterized by painless bilateral cervical
Dan Liu, Xia Liu, Yi Sha Liu, Chao Xin Zhou   +3 more
doaj   +1 more source

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

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   +1 more source

A case of disseminated extranodal Rosai–Dorfman disease diagnosed by skin manifestations

Journal of Cutaneous Immunology and Allergy, 2023
Rosai–Dorfman disease (RDD) is a rare non‐Langerhans cell histiocytosis that was first described as sinus histiocytosis with massive lymphadenopathy by Rosai and Dorfman in 1969.
Shintaro Saito, Akihiko Uchiyama, Yayoi Shibusawa, Sei‐ichiro Motegi   +3 more
doaj   +1 more source

Cutaneous Rosai–Dorfman disease with MAP2K1 mutation, initially mimicking an infection with parasitized histiocytes

Journal of Cutaneous Pathology, Volume 51, Issue 12, Page 942-947, December 2024.
Abstract Rarely, Rosai–Dorfman disease (RDD) manifests exclusively in the skin, typically as nodules on the trunk and extremities. Recognition of characteristic histopathologic features enables diagnosis of RDD. A 55‐year‐old female presented with a 7‐year history of cutaneous nodules involving the trunk and extremities. A prior skin biopsy specimen at
Joseph Gillam, Ruchi Desai, Raphael J. Louie, Scott A. Turner, Grace Y. Wang, Julio A. Diaz‐Perez, Mark C. Mochel   +6 more
wiley   +1 more source

Idiopathic multicentric Castleman disease with marrow fibrosis and extramedullary hematopoiesis

European Journal of Haematology, Volume 113, Issue 6, Page 833-841, December 2024.
Abstract Background Idiopathic multicentric Castleman disease (iMCD) is a rare inflammatory disorder mediated by excessive proinflammatory cytokine signaling, most notably by interleukin 6 (IL‐6). IL‐6‐induced extramedullary hematopoiesis (EMH) has been reported in murine models of iMCD. Herein we present four cases of iMCD with EMH in humans.
Marley Blommers, Sorin Selegean, Richard K. Wood, Mateo Sarmiento Bustamante, Saishravan Shyamsundar, E. Ashley Wiley, Emilie Comeau, Allam A. Shawwa, Stefan Rose‐John, David C. Fajgenbaum, Luke Y. C. Chen   +10 more
wiley   +1 more source

Rosai-Dorfman syndrome associated with systemic erythematous lupus: case report [PDF]

, 2019
Objetivo: Relatar um caso de associação de Síndrome de Rosai-Dorfman e Lúpus Eritematoso Sistêmico acompanhado no ambulatório de Clínica Médica de nosso Hospital Universitário.
Bastos, Stéphany Oliveira, Roballo, Carla Adriane, Sales, Guilherme Moura, Soares, Renata Fernandes Mendes   +3 more
core   +2 more sources

Diagnosis of sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) by fine needle aspiration cytology

Journal of Cytology, 2009
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease) is a rare benign disease of unknown etiology presenting with massive lymphadenopathy. These cases can often be misdiagnosed as lymphoma.
Kushwaha Rashmi, Ahluwalia Charanjeet, Sipayya Varuna   +2 more
doaj  

Orbital Rosai–Dorfman disease: a case report and literature review

Journal of International Medical Research, 2019
We report a case of orbital Rosai–Dorfman disease in a 45-year-old man who presented with exophthalmos as the first symptom for 6 months. He did not have any itching, photophobia, tears, headache, dizziness, nausea, vomiting, or other symptoms of ...
Xin Su, Liqing Zhang
doaj   +1 more source

A Rare Case of Multiorgan Involvement of Rosai Dorfman Disease in an Elderly Female

Journal of Nepal Medical Association, 2014
Sinus histiocytosis with massive lymphadenopathy (SHML), Rosai-Dorfman Disease, is a rare histiocytic syndrome first described by Rosai and Dorfman, most frequently seen in children and young adults.The disease is more common in males and in individuals ...
Rakesh Digambar Waghmare
doaj   +1 more source

A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease

iRADIOLOGY, EarlyView.
Lin Chen, Rui Zhou
wiley   +1 more source