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Sinus histiocytosis with massive lymphadenopathy

MONDO:0006412

A rare disorder of unknown etiology characterized by distention of the lymph node sinuses and sinusoidal histiocytic infiltration. The histiocytes characteristically contain ingested lymphocytes. Patients present with cervical lymphadenopathy, fever, leukocytosis, and hypergammaglobulinemia. It can affect extranodal sites, including skin, bones, and the respiratory tract. It usually regresses spontaneously.

Also known as: Destombes-RosaC/-Dorfman disease, Destombes-Rosaï-Dorfman disease, RDD, RosaC/-Dorfman-Destombes disease, Rosai-Dorfman Disease, Rosai-Dorfman disease, Rosaï-Dorfman-Destombes disease, SHML

16 clinical trials for this condition and its sub-types, 11 tagged with Sinus histiocytosis with massive lymphadenopathy itself.

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Sub-types of Sinus histiocytosis with massive lymphadenopathy

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