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Concomitant sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease) and diffuse large B-cell lymphoma: a case report [PDF]

Journal of Medical Case Reports, 2008
Introduction Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman Disease, is a rare and benign source of lymphadenopathy first described in 1969, which mimics neoplastic processes.
Moore James C, Zhao Xiaohui, Nelson Edward L   +2 more
doaj   +3 more sources

Paranasal Rosai-Dorfman Disease with Osseous Destruction [PDF]

Case Reports in Otolaryngology, 2017
Rosai-Dorfman disease is a rare histiocytic proliferative disorder of unknown etiology typically characterized by cervical lymphadenopathy. Extranodal involvement often manifests in the head and neck region. We present a 10-year-old male who presented to
Kevin Hur, Changxing Liu, Jeffrey A. Koempel   +2 more
doaj   +8 more sources

Rosai-Dorfman Disease Involving Multiple Organs: An Unusual Case with Poor Prognosis [PDF]

Case Reports in Medicine, 2016
Rosai-Dorfman disease is a rare, benign histiocytic proliferative disorder that usually affects the lymph nodes. Although extranodal involvement has been reported in diverse sites, manifestation in the cardiovascular system is extremely rare ...
Fandresena Arilala Sendrasoa, Irina Mamisoa Ranaivo, Onivola Raharolahy, Malalaniaina Andrianarison, Naina Harinjara Razanakoto, Lala Soavina Ramarozatovo, Fahafahantsoa Rapelanoro Rabenja   +6 more
doaj   +4 more sources

Rosai-Dorfman disease of the oral cavity [PDF]

Autopsy and Case Reports, 2023
First described by J Rosai and R F Dorfman in 1969, Rosai-Dorfman disease (RDD) is a benign, self-limiting histiocytosis of unknown etiology. It is usually seen in the first two decades of life.
Abir Charfeddine, Mounir Omami, Marwa Garma, Ahlem Bellalah, Sameh Sioud, Jamil Selmi   +5 more
doaj   +3 more sources

Intracranial Rosai-Dorfman Disease [PDF]

Case Reports in Radiology, 2014
Rosai-Dorfman disease (RDD) is a rare, benign pseudolymphomatous condition, predominantly involving lymph nodes. Rosai-Dorfman disease (RDD) (sinus histiocytes with massive lymphadenopathy) rarely affects the intracranial region without involvement of ...
Yadav Arun Kumar, Peng Yi Peng, Xia Chen Chen   +2 more
doaj   +2 more sources

Rosai-Dorfman Disease Originating from Nasal Septal Mucosa [PDF]

Case Reports in Otolaryngology, 2015
Rosai-Dorfman disease is a rarely seen disease with unknown etiology. Extranodal involvement is most commonly seen in the head and neck region. Histopathologically, it is characterized by histiocytic cell proliferation. This paper presents a case of a 15-
Abdulvahap Akyigit, Hadice Akyol, Oner Sakallioglu, Cahit Polat, Erol Keles, Ozkan Alatas   +5 more
doaj   +3 more sources

Anaesthesia for proximal femoral nailing in a patient with “Rosai Dorfman disease” with prior laryngotracheal reconstruction - Not all rosy as it seems [PDF]

Trauma Case Reports
Rosai Dorfman disease is a rare disease with massive lymphadenopathy. It presents significant challenges to the anaesthesiologists involving multiple organs especially the airway.
Ashna Shetty, Megha Thaleppady, Priyanka Mahanta, Shilpa A Naik, Akanksha Chouhan   +4 more
doaj   +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

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

A Single Case of Rosai–Dorfman Disease Marked by Pathologic Fractures, Kidney Failure, and Liver Cirrhosis Treated with Single-Agent Cladribine [PDF]

Frontiers in Oncology, 2014
Rosai-Dorfman disease (RDD) is a proliferative histiocytic disorder of unknown etiology, which is characterized by sinus histiocytosis with massive lymphadenopathy (1). In most cases, RDD has a benign course and treatment is not necessary. However, severe cases of RDD require treatment, and the treatment strategy is determined on the basis of the ...
Sasaki, Koji, Pemmaraju, Naveen, Westin, Jason R., Wang, Wei-Lien, Khoury, Joseph D., Podoloff, Donald A., Moon, Bryan, Daver, Naval, Borthakur, Gautam   +8 more
openaire   +3 more sources