Sustained remission of Sézary syndrome.

Eur J Dermatol

Department of Dermatology, Mayo Clinic, 200 First Street SW Rochester, Minnesota 55905, USA.

Published: May 2002

AI Article Synopsis

  • Sézary syndrome is a severe form of cutaneous T-cell lymphoma characterized by circulating malignant T cells (Sézary cells) that cause various skin and systemic symptoms, including intense itching and painful lesions.
  • The main symptoms include exfoliative erythroderma, alopecia, and generalized lymphadenopathy, leading to significant discomfort and disfigurement for patients.
  • Extracorporeal photopheresis has emerged as a key treatment, and in one unique case, a patient achieved sustained remission for two years after receiving this therapy alone, highlighting its potential effectiveness.

Article Abstract

Sézary syndrome, an aggressive form of cutaneous T-cell lymphoma, is a devastating, highly symptomatic form of non-Hodgkin lymphoma. Malignant clones of mature helper CD4 T cells containing large, convoluted nuclei known as Sézary cells circulate in the blood and infiltrate the skin. Clinical features include exfoliative erythroderma, generalized lymphadenopathy, alopecia, onychodystrophy, palmoplantar hyperkeratosis, and ectropion. Patients often have severe pruritus, burning sensations, pain, bleeding from excoriations, and disfigurement. Extracorporeal photopheresis, an immunomodulatory therapy, has become a primary therapy for these patients. This pheresis-based therapy uses psoralen and ultraviolet A radiation-mediated photochemotherapy to induce immune responses. The effects of extracorporeal photopheresis vary considerably. We report sustained remission (2 years) in a patient with Sézary syndrome. Previously he had received extracorporeal photopheresis and interferon alfa-2b injections. He is the only one of 55 patients with Sézary syndrome treated at Mayo Clinic (Rochester, Minnesota, USA) to achieve sustained remission on extracorporeal photopheresis alone.

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