Sezary syndrome


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Related to Sezary syndrome: mycosis fungoides

Sezary syndrome

[sə′zar·ē ‚sin‚drōm]
(medicine)
Exfoliative erythroderma with a cutaneous infiltrate of atypical mononuclear cells; similar cells are also present in the peripheral blood.
References in periodicals archive ?
Coverage of the Sezary Syndrome pipeline on the basis of route of administration and molecule type.
Molecular cytogenetic analysis of cutaneous T-cell lymphomas: identification of common genetic alterations in Sezary syndrome and mycosis fungoides.
59 Recently, the case of a 50 year-old man with a diagnosis of Sezary syndrome and seronegative rheumatoid arthritis was reported as being successfully treated with ECP (60).
Mycosis fungoides and Sezary syndrome are not associated with HTLV-1 infection: An international study.
Sezary syndrome is a rare disease characterized by erythroderma, lymphadenopathy, and a neoplastic T-cell population involving skin, lymph nodes, and peripheral blood.
Prognostic factors and evaluation of mycosis fungoides and Sezary syndrome.
Hydantoin-induced cutaneous pseudolymphoma with clinical, pathologic and immunologic aspects of Sezary syndrome.
ClickPress, Thu Apr 09 2015] GlobalData's clinical trial report, "Sezary Syndrome Global Clinical Trials Review, H1, 2015" provides data on the Sezary Syndrome clinical trial scenario.
small/medium T-cell lymphoma (PC-SMTCL) began in the early 1990s when the updated Kiel classification system (1,2) was applied to primary cutaneous T-cell lymphomas that did not meet criteria for mycosis fungoides (MF) or Sezary syndrome.