Results 41 to 50 of about 111,579 (167)

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

Case series: Kikuchi‐Fujimoto disease with diagnostic overlap

Rheumatology &Autoimmunity, Volume 6, Issue 3, Page 198-201, September 2026.
Kikuchi‐Fujimoto disease (KFD) is a rare, self‐limiting necrotizing lymphadenitis that poses significant diagnostic challenges due to its overlap with tuberculosis, systemic lupus erythematosus (SLE), and malignancy. We present four cases highlighting distinct diagnostic complexities: KFD mimicking tuberculosis with concomitant latent TB infection and ...
Ecem Kalemoglu, Ming Zheng, Danny Arias, Andreina M. Paulino, Aisha Niaz, James Devlin, Valentin Marian   +6 more
wiley   +1 more source

Doença de Rosai-Dorfman cutânea: relato de caso Cutaneous Rosai-Dorfman disease: a case report

Anais Brasileiros de Dermatologia, 2010
A doença de Rosai-Dorfman, também denominada histiocitose sinusal com linfadenopatia maciça, é histiocitose de células não Langerhans, idiopática e de curso benigno.
Josie da Costa Eiras, Antônio Pedro Mendes Schettini, Livia Lima de Lima, Liana Hortência Miranda Tubilla, Rosa Maria Libório de Oliveira   +4 more
doaj   +1 more source

Multiple Inflammatory Scalp Nodules in an Infant: A Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Multiple scalp nodules in infancy warrant cautious interpretation, as their extent and pattern may signal conditions requiring broader evaluation than localized infection. Avoiding premature diagnostic labels and relying on careful visual assessment helps ensure timely investigation, appropriate therapy, and prevention of long‐term cutaneous ...
Chukwuka Elendu, Mbanefo C. Uyanwune
wiley   +1 more source

Sinus histiocytosis with massive lymphadenopathy, (Rosai-Dorfman Disease) with cholastatic jaundice in an HIV positive patient [PDF]

, 2018
IntroductionSinus histiocytosis with massive lymphadenopathy is a rare histiocytic disease first described by Rosai and Dorfman in 1969. The typical presentation is that of cervical and often widespread painless lymphadenopathy.Case reportWe present a 33-
Kgomo Mpho; Department of Gastroenterology, University of Pretoria, South Africa, Ngwata Portia; Department of Gastroenterology, University of Pretoria, South Africa, Mashoshoe Kgataki Sam; Department of Gastroenterology, University of Pretoria, South Africa, Bida Mishack; Department of Anatomical Pathology, University of Pretoria, South Africa, Elnagar Ali Ahmed; Department of Gastroenterology, University of Pretoria, South Africa, Thomas Preetha; Department of Gastroenterology, University of Pretoria, South Africa   +5 more
core  

Rosai-Dorfman Disease with Hypercalcemia and Acute Renal Failure

Turkish Journal of Nephrology, 2019
Rosai-Dorfman Disease is a granulomatous disease of unknown etiology that is characterized by painless massive lymphadenopathy. It is also known as Sinus histiocytosis. Acute renal failure with sinus histiocytosis has been reported very rarely.
Melahat ÇOBAN, Refik OLMAZ, Ayşe AKARSU, Ayça İNCİ, Semih GÜL, Metin SARIKAYA   +5 more
doaj  

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

H Syndrome Associated With Pure Red Cell Aplasia, Rosai–Dorfman Disease, and Sensorineural Hearing Loss: Phenotypic Variability in Three Children With the Same SLC29A3 Mutation

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT H syndrome is a rare autosomal recessive disorder caused by mutations in the SLC29A3 gene. We report three pediatric patients with a homozygous c.1309G>A (p.Gly437Arg) mutation presenting with distinct phenotypic variations. These cases expand the clinical spectrum and emphasize the importance of early genetic diagnosis and family counseling.
Mohammad Najajrah, Hadeel I. Bouzia, Nermin K. Darawi, Fatima S. Hajjaj, Nour H. Moosa, Noor M. Awad   +5 more
wiley   +1 more source

Chronic Recurrent Multifocal Osteomyelitis in a Pediatric Patient: An Uncommon Case With Diagnostic Challenge

Clinical Case Reports, Volume 14, Issue 8, August 2026.
ABSTRACT Chronic Recurrent Multifocal Osteomyelitis (CRMO) is a rare autoinflammatory bone disorder that primarily affects children and adolescents. It is characterized by recurrent episodes of bone pain with sterile inflammatory lesions, often resembling infection or malignancy.
Dosti Regmi, Madhur Bhattarai, Sujata Bhandari, Saurav Jha, Akriti Baral   +4 more
wiley   +1 more source

Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital

Nigerian Dental Journal, 2011
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare, benign disease of unknown aetiology. This disease typically presents with massive, painless cervical lymphadenopathy but may occur in a wide variety of extranodal sites.
O. F. Ajayi, O. A. Effiom, W. L. Adeyemo, O. M. Gbotolorun, W. Akinshipo   +4 more
doaj   +1 more source