Results 11 to 20 of about 11,417 (249)

Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]

, 2018
The described clinical case presents 39-year-old patient with no clinically significant accompanying diseases. Since the beginning of October 2015, the patient has complained of fever, abdominal pain and generalized enlarged lymph nodes.
Gercheva, Liana, Spasova, Snejana, Varbanov, Hinko, Yuzeir, Sheniz   +3 more
core   +4 more sources

Intrathoracic Rosai-Dorfman Disease in Elderly Patients: A Case Report. [PDF]

Clin Case Rep
ABSTRACT Rosai–Dorfman disease (RDD), a rare form of histiocytosis, predominantly affects young individuals. Clinically categorized into nodal and extranodal subtypes, the disease primarily involves systemic lymph nodes with possible involvement of other organs.
Xiao J, Ma L, Cao W.
europepmc   +2 more sources

Rosai–Dorfman Disease: A Rare Clinicopathological Presentation and Review of the Literature

Head and Neck Pathology, 2020
Aileen Azari-Yam, Mohammad Reza Abdolsalehi, Mohammad Vasei, Moeinadin Safavi, Mehrzad Mehdizadeh   +4 more
openalex   +3 more sources

Rosai-Dorfman Disease in a 4-Month-Old Female Presenting With Cervical Lymphadenopathy. [PDF]

Clin Case Rep
ABSTRACT Rosai‐Dorfman disease is a rare histiocytic disorder that can mimic malignancies. This case highlights the importance of immunohistochemistry in distinguishing RDD from lymphoproliferative neoplasms, ensuring accurate diagnosis and management.
Khan A, Malik A, Sadiq MH, Arshad MS, Safdar F, Antar M.   +5 more
europepmc   +2 more sources

Rosai-Dorfman disease mimicking gastrointestinal tuberculosis and fungal sinusitis: A case report

Radiology Case Reports, 2022
Every organ can be affected by Rosai-Dorfman disease, the most common being skin and soft tissue, bone and upper respiratory tract. Here we present a Rosai-Dorfman disease patient who manifested with multiple organ involvement.
Seid Getahun Abdela, MD, Chalew Abebe Mengesha, MD   +1 more
doaj   +1 more source

Neuropsychological Aspects of a Patient With Intracranial Rosai-Dorfman Disease: Case Report. [PDF]

Clin Case Rep
ABSTRACT Intracranial Rosai‐Dorfman disease (RDD) is rarely reported in the literature. Up to the present date, there are no documented studies regarding the neuropsychological aspects of a patient with this diagnosis. This study fills this gap, reporting a case of a patient with petroclival RDD, emphasizing the importance of cognitive investigation.
Veras C, de Oliveira DS, Dos Santos SRZ, Ferreira LFL, Filho CAFA, Côrtes BA, Charchat-Fichman H.   +6 more
europepmc   +2 more sources

Rosai–Dorfman Disease between Proliferation and Neoplasia

Cancers, 2022
Simple Summary Rosai–Dorfman disease (RDD) was a benign histiocytic proliferative disorder rather than a neoplastic process. Emergent molecular studies have shown recurrent somatic gain-of-function mutations in genes of the MAPK pathway (e.g., NRAS, KRAS,
Ismail Elbaz Younes, L. Sokol, Ling Zhang   +2 more
semanticscholar   +1 more source

Temporal bone manifestation of primary extranodal Rosai–Dorfman disease: a case report

Journal of Medical Case Reports, 2023
Background Rosai–Dorfman disease is a rare benign histiocytic disorder characterized in most cases by painless cervical adenopathy. Less than 10% of extranodal cases involve bony lesions. Primary bone Rosai–Dorfman disease in the absence of nodal disease
E. Koonar, F. Ramazani, M. Hyrcza, J. Chau   +3 more
doaj   +1 more source

Outcomes After Treatment With Cobimetinib in Patients With Rosai-Dorfman Disease Based on KRAS and MEK Alteration Status.

JAMA Oncology, 2022
Importance Rosai-Dorfman disease (RDD) is a rare histiocytic neoplasm with recent studies showing alterations in the MAPK pathway, most commonly in the KRAS and MEK genes in about 40% of patients.
J. Abeykoon, K. Rech, J. Young, A. Ravindran, G. Ruan, S. Dasari, D. Morlote, R. King, Claire Rummage, S. Zanwar, Aldo M Acosta-Medina, W. Tobin, M. Shah, N. Bennani, R. Vassallo, J. Ryu, M. Koster, Caroline Davidge-Pitts, T. Witzig, G. Goyal, R. Go   +20 more
semanticscholar   +1 more source

Emergence of cutaneous Rosai–Dorfman disease during immunosuppressive treatment of follicular B-cell lymphoma: A case report

SAGE Open Medical Case Reports, 2021
Background: Sinus histiocytosis with massive lymphadenopathy, also known as Rosai–Dorfman disease, is a rare proliferation of non-Langerhans histiocytes.
Sharon L Kipfer, Michael Samycia, Carolyn J Shiau   +2 more
doaj   +1 more source