Results 31 to 40 of about 1,868 (215)

Intracranial Rosai-Dorfman Disease: pathophysiology, diagnosis and treatment [PDF]

, 2022
Introduction and purpose: ​Rosai-Dorfman Disease (RDD), known also as sinus histiocytosis with massive lymphadenopathy(SHML) is a benign histiocytic proliferative syndrome. The etiology and pathogenesis of RDD remains unclear.
Dryla, Aleksandra, Kamieniak, Piotr, Pytka, Michalina, Szymoniuk, Michał   +3 more
core   +2 more sources

A Rare Cause of Lymphadenopathy in a Young Hispanic Female: Unmasking Recurrent Nodal Rosai-Dorfman Disease [PDF]

, 2023
Rosai-Dorfman disease (RDD) is a rare histiocytic disorder that can present with painless bilateral symmetrical cervical lymphadenopathy, mimicking lymphomas.
Alfarooq Alshaikhli, Blesset Alexander, Emilia C Dulgheru, Mery Bartl, Yilen K Ng-Wong   +4 more
core   +2 more sources

Rosai-Dorfman Disease: Rare Pulmonary Involvement Mimicking Pulmonary Langerhans Cell Histiocytosis and Review of the Literature

Case Reports in Radiology, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare nonmalignant lymphohistiocytic proliferative disorder.
Rashid AL Umairi, Danielle Blunt, Wedad Hana, Matthew Cheung, Anastasia Oikonomou   +4 more
doaj   +1 more source

Rosai-Dorfman disease in a patient with cervical lymphadenopathy and associated Serratia marcescens infection

Clinical Infection in Practice, 2020
Sinus histiocytosis with massive lymphadenopathy (SHML), also known as Rosai-Dorfman disease (RDD), is a rare idiopathic, non-neoplastic proliferative disorder of histiocytes with an unknown etiology that most often presents as bilateral painless ...
Alvaro E. Galvis, Korena Boyd, Iris S. Pecson   +2 more
doaj   +1 more source

Primary Rosai-Dorfman Disease in 39-Year-Old Woman With Osseous Tibial Lesion Manifestion: A Case Report and Literature Review

Foot & Ankle Orthopaedics, 2021
Rosai-Dorfman disease (RDD), otherwise known as sinus histiocytosis with massive lymphadenopathy (SHML), is a very rare and typically benign disorder of unknown etiology with
Jasmin Mansoori DPM, Olivia Fisher MD, MPH, Ivana O. Akinyeye DPM, Michael A. Sobolevsky DPM, Robert H. Quinn MD   +4 more
doaj   +1 more source

A patient with a papulo‐nodular lesion on the shoulder

, 2023
JEADV Clinical Practice, Volume 2, Issue 3, Page 662-665, September 2023.
Fanny Ickx, Axel De Greef, Diane Declaye, Léo‐Paul Secco, Marie Baeck   +4 more
wiley   +1 more source

Primary intraosseous manifestation of Rosai-Dorfman disease: 2 cases and review of literature

Journal of the Belgian Society of Radiology, 2014
Rosai-Dorman disease (RDD) is a rare disorder of proliferative histiocytes with an unknown etiology. It is also known as sinus histiocytosis with massive lymphadenopathy. Most patients present with painless cervical lymphadenopathy due to accumulation of
H M Duijsens, F M Vanhoenacker, B P Braak ter, P C Hogendoorn, H M Kroon   +4 more
doaj   +1 more source

Rosai-Dorfman Disease: Self-Resolving Unilateral Lymphadenopathy and a Brief Review of Literature

Case Reports in Oncological Medicine, 2018
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is a disease of histiocytic proliferation with no known pathogenesis.
Joshua Feriante, Richard T. Lee
doaj   +1 more source

Nodal histiocytic disorder in children: report of three cases and review of literature

The Egyptian Journal of Otolaryngology, 2020
Background Histiocytic system consists of phagocytes and dendritic cells. Both are found in lymph nodes. Usually, this disorder presents with painless cervical lymph node enlargement hence frequently mistaken for lymphoma or tuberculosis.
Indumathi Ainer, Hardip Singh Gendeh, Salina Binti Husain, Khadijah Mohd Nor   +3 more
doaj   +1 more source

Extranodal manifestation of Rosai-Dorfman disease with bilateral ocular involvement

Journal of Cytology, 2011
Rosai-Dorfman disease, that is, sinus histiocytosis with massive lymphadenopathy is a benign systemic proliferative disorder of histiocytes. The typical clinical presentation of the disease includes bilateral painless massive lymphadenopathy, fever and ...
Chayanika Kala, Asha Agarwal, Sanjay Kala   +2 more
doaj   +1 more source