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Rosai dorfman disease of the orbit [PDF]
This is an Open Access article distributed under the terms of the Creative Commons Attribution ...
Honavar, Santosh G+2 more
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Key Clinical Message Intracranial RDD is rare medical event mimicking different diagnoses. Although the surgical resection is the best treatment option, but radiation therapy can also achieves long‐term suboptimal outcomes. Abstract An 83‐year‐old male with a history of tension‐type headaches was evaluated.
Hamid Nasrollahi+6 more
wiley +1 more source
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
Diagnostic challenges in Rosai-Dorfman-Destombes disease (case description and literature review) [PDF]
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+3 more
core +2 more sources
Rosai-Dorfman disease is a benign, self-limited, idiopathic proliferative histiocytic disorder. It was first described in 1969 by Rosai and Dorfman. In its typical form the disease is characterized by extensive cervical lymphadenopathy associated with ...
Paula Azevedo Borges Leal+5 more
doaj
Sinus Histiocytosis with Massive Lymphadenopathy (Rosai Dorfman Disease) and Anaplastic Large Cell Lymphoma [PDF]
Sinus histiocytosis with massive lymphadenopathy (SHML) is a rare and benign source of lymphadenopathy first described in 1969. This disease commonly presents in children and young adults with supra-diaphragmatic lymphadenopathy mainly at cervical nodal ...
Garg, Kapil Kumar, Singh, Harpreet
core +1 more source
Rosai-Dorfman Disease: A Diagnostic Albatross in a Female Patient with Bilateral Persistent Neck Masses. A Case Report [PDF]
RosaiDorfman disease (sinus histiocytosis with massive lymphadenopathy) is an uncommon benign and often self limiting lymphoproliferative disease of unknown aetiology which was first described by Rosai and Dorfman in 1969.
Akinbohun, AO+4 more
core +2 more sources
Sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman Disease): Report of a case in a Nigerian Teaching Hospital [PDF]
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.
Adeyemo, W. L.+4 more
core +2 more sources
A 55‐year‐old man with a cerebral mass
Brain Pathology, Volume 34, Issue 6, November 2024.
Serena Ammendola+2 more
wiley +1 more source
A Case of Rosai-Dorfman Disease with Highly Elevated Serum Ferritin [PDF]
Sinus histiocytosis with massive lymphadenopathy, also known as Rosai-Dorfman disease is a rare disorder characterized by proliferation of distinctive histiocytes within lymph node sinuses and lymphatics, sometimes involving extranodal sites.
Chen+11 more
core +2 more sources