Results 71 to 80 of about 6,612 (227)

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

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

Rosai-Dorfman disease presenting as stridor and hoarseness in a young female patient

Radiology Case Reports, 2023
Rosai-Dorfman disease is a non-Langherans cell histiocytosis typically revealed by lymphadenopathy. Extranodal involvement occurs in 43% and most commonly involves the head and neck, skin, and bones. Few reports have described laryngeal lesions.
Vivianne Kokje, MD, PhD, Claudio De Vito, MD, PhD, Flavia Costa Varela, MD, Yan Monnier, MD, PhD, Nicolas Dulguerov, MD, Minerva Becker, MD, Maxime Mermod, MD, PhD   +6 more
doaj  

Isolated unilateral eyelid Rosai–Dorfman disease

Oman Journal of Ophthalmology, 2018
Isolated eyelid Rosai–Dorfman disease without orbital disease or systemic involvement is very rare and needs a high degree of suspicion. In this report, we describe a 16-year-old boy who presented with isolated eyelid Rosai–Dorfman disease involving the ...
Nandini Bothra, Swathi Kaliki, Swarnalata Gowrishankar, S Anuradha   +3 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

Disseminated histiocytoses biomarkers beyond BRAFV600E: frequent expression of PD-L1. [PDF]

, 2015
The histiocytoses are rare tumors characterized by the primary accumulation and tissue infiltration of histiocytes and dendritic cells. Identification of the activating BRAFV600E mutation in Erdheim-Chester disease (ECD) and Langerhans cell histiocytosis
Arceci, Robert J, Bender, Ryan P, Bilalovic, Nurija, Gatalica, Zoran, Millis, Sherri Z, Palazzo, Juan P., Swensen, Jeffrey, Von Hoff, Daniel, Vranic, Semir   +8 more
core   +3 more sources

Erdheim–Chester disease: An elusive diagnosis in a 50‐year‐old Ethiopian man presenting with diffuse sclerotic bone lesion

Clinical Case Reports, Volume 12, Issue 9, September 2024.
Key Clinical Message Diagnosis of Erdheim–Chester disease (ECD) requires the clinician to be familiar with its various manifestations, classic radiologic and histologic features. This case highlights the significance of considering ECD in any patient presenting with bone pain and symmetric osteosclerosis of long bones of extremities to allow for early ...
Semir Abdi Usmael, Addisu Alemu Gebrehiywot, Ashenafi Lemma Bekele, Solomon Bishaw Yezengaw, Tekalign Tsegaye Tefera, Hunduma Bikila Bote, Kalkidan Abera Shibeshi, Anteneh Belachew Fantaye   +7 more
wiley   +1 more source

Review and a case of rare Rosai-Dorfman disease

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   +1 more source

Steroid responsive cavernous sinus syndrome due to Rosai-Dorfman disease: beyond Tolosa-Hunt syndrome – a case report

BMC Neurology, 2021
Background The term “Tolosa-Hunt syndrome” (THS) has been used to refer to painful ophthalmoplegia associated with nonspecific inflammation of the cavernous sinus and many processes can result in a similar clinical picture, including infectious ...
Paulo Ribeiro Nóbrega, Pedro Gustavo Barros Rodrigues, Isabelle de Sousa Pereira, Carolina de Figueiredo Santos, Gunter Gerson, José Arnaldo Motta de Arruda, José Wagner Leonel Tavares Júnior, Pablo Picasso de Araújo Coimbra, Pedro Braga-Neto   +8 more
doaj   +1 more source

Rosai-Dorfman Disease: A previously unreported association with Sickle Cell Disease [PDF]

, 2007
BACKGROUND: Rosai-Dorfman Disease is an uncommon benign systemic histio-proliferative disease. This is the first time the disease, although more common in people of African descent, is described in association with Sickle cell disease. CASE PRESENTATION:
Inusa, Baba, Ramadan, Ghada, Stebbing, Claire, van der Walt, Jon   +3 more
core   +2 more sources