Results 51 to 60 of about 6,572 (224)

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

Rosai Dorfman Disease: A Rare Cause of Cervical Lymphadenopathy [PDF]

National Journal of Laboratory Medicine, 2018
Rosai Dorfman disease, a sinus histiocytosis, is rare to find and difficult to diagnose. It may masquerade as commoner diseases including infections and malignancies.
Sreenath Sreenivasan, Kiren George Koshy, Santhosh Kumar TS, Jasen Joseph, T Anuvind   +4 more
doaj   +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

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

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

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

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  

Extranodal manifestation of Rosai-Dorfman disease in the breast tissue [PDF]

, 2016
A 71-year-old asymptomatic female with a history of breast cancer status after right total mastectomy had interval development of several new nodules in the left breast in a 1-year time span.
Ansari, Umer, Cundiff, Maria, Davis, Fiona, Keshav, Nandan, Zhou, Qiao   +4 more
core   +1 more source

A Rare Case of Primary Intraparenchymal Rosai‐Dorfman Disease

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

Common progenitor origin for Rosai–Dorfman disease and clear cell sarcoma

The Journal of Pathology, Volume 264, Issue 3, Page 243-249, November 2024.
Abstract Histiocytic neoplasms (HNs) in adults have been reported to be associated with a high prevalence of coexisting haematological and solid malignancies. While a proportion of coexisting HNs and haematological malignancies share identical genetic alterations, the genetic association between HNs and solid malignancies has scarcely been reported. We
Aki Sato, Nozomi Yusa, Hiroyuki Takamori, Eigo Shimizu, Kazuaki Yokoyama, Satoshi Ichikawa, Hisayuki Yokoyama, Yuki Kasahara, Kodai Enda, Fumiyoshi Fujishima, Ryo Ichinohasama, Yasunori Ota, Seiya Imoto, Yasuhito Nannya   +13 more
wiley   +1 more source