Results 41 to 50 of about 7,279 (231)
Asymptomatic flow of Rosai-Dorfman disease [PDF]
, 2014 Introduction. Sinus histiocytosis with massive lymphadenopathy is a rare benign self-limiting disease of unknown etiology. The salivary gland involvement, indicating the extranodal character of the disease, often presents a diagnostic dilemma ...
Bjelaković Bojko +10 more
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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 +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 +8 more
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Otolaryngology Case Reports, 2022 Rosai-Dorfman disease is a rare non-Langerhans cell histiocytosis which classically presents with cervical lymphadenopathy. Extranodal disease in the head and neck is uncommon.
Melissa M. Liu +2 more
doaj +1 more source
Isolated intraventricular Rosai–Dorfman disease
Asian Journal of Neurosurgery, 2018 Rosai–Dorfman disease (RDD) is a benign histioproliferative disorder characterized by generalized lymphadenopathy, weakness, anemia, and rarely extranodal involvement. The disease affects the central nervous system (CNS) very rarely and at a relatively older age. Isolated intracranial involvement is very rare.
Patwardhan, Pranav Pramod +1 more
openaire +3 more sources
IDCases, 2020 Rosai-Dorfman disease (RDD) a rare, non-malignant disease of histiocytic proliferation usually presents as a painless lymphadenopathy. It has been associated with autoimmune diseases, viral infections, and malignancies.
Alejandro Olmedo-Reneaum +3 more
doaj +1 more source
Pleomorphic cutaneous Rosai–Dorfman disease
Histopathology, 2016 we report three cases of pure cutaneous Rosai-Dorfman disease (RDD) showing prominent nuclear pleomorphism. This unusual finding confers a worrisome appearance to these lesions, challenging their recognition and creating difficulty in the differential diagnosis with malignant neoplasms. This article is protected by copyright. All rights reserved.
Carolina Martínez‐Ciarpaglini +6 more
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Pediatric Hematology Oncology Journal, 2019 Rosai Dorfman disease (RDD) commonly presents as bilateral cervical lymphadenopathy in children and young adults. We herein report a young girl with unilateral inguinal lymphadenopathy as a rare presentation of RDD. Keywords: Child, Rosai Dorfman disease,
Rakesh Kumar Pilania +3 more
doaj +1 more source
Extranodal rosai dorfman disease: a case report of single soft tissue cystic lesion [PDF]
, 2020 Rosai-Dorfman disease (RDD) is an uncommon benign histiocytic disorder. It is found worldwide and slightly more common among in men (1.4:1), affecting individuals are with an average age of 20.6 years. Extranodal tissue involvement is documented in 25-43%
Agrawal, Ruchi +2 more
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Bilateral breast Rosai‐Dorfman disease screen detected by mammography
Clinical Case Reports, 2023 Rosai‐Dorfman disease (RDD) is a proliferative disorder of histiocytes typically found in nodal sites and commonly observed in females. Patients often present with systemic symptoms such as fever, lymphadenopathy, and weight loss.
Christina Sumner +6 more
doaj +1 more source