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International Journal of Complementary and Internal Medicine

  • CASE REPORT
     

Beyond Eczema and Lupus: Sézary Syndrome with Chronic Cutaneous Presentation Mimicking Common Inflammatory Dermatoses
 

  • Carmen Cecilia Tamara Ariza.1 Alexander Jesus Diaz Navarro.1 Marco Antonio Ditta Cassiani.1 Angelo Geovanni Arzuaga Hernández.2 Jose Francisco Vega Romero.3,4 María José Viera Contreras.5

    .1Internal medicine, Metropolitan University, Barranquilla, Colombia 
  • .2Department of Rheumatology, Comprehensive Rheumatology Center of the Caribbean, Barranquilla, Colombia 
  • .3Medicine, Sinu University, Cartagena, Colombia 
  • .4Medicine, Metropolitan University, Barranquilla, Colombia 
  • .5Internal medicine, Simon Bolivar University, Barranquilla, Colombia

    Corresponding Author: Carmen Cecilia Ariza Tamara. Metropolitan University, Barranquilla/Colombia, 76th Street No. 42-78 Garden City Neighborhood, Barranquilla, Atlántico. E-mail: [email protected]

    Received: November 11, 2025                                    Published: November 21, 2025

    Citation: Ariza Tamara CC. Beyond Eczema and Lupus: Sézary Syndrome with Chronic Cutaneous Presentation Mimicking Common Inflammatory Dermatoses. Int J Complement Intern Med. 2025;6(4):469–474. DOI: 10. 58349/IJCIM. 4. 6. 2025. 00166

    Copyright: ©2025 Ariza Tamara CC. This is an open access article distributed under the terms of the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and build upon your work non-commercially.

    Abstract 

Sézary syndrome is an uncommon and aggressive leukemic variant of cutaneous T-cell lymphoma (CTCL), often misdiagnosed in its early stages due to its clinical resemblance to chronic inflammatory dermatoses such as eczema or cutaneous lupus erythematosus. We report the case of a 67-year-old woman who presented with chronic pruritic erythematous plaques initially diagnosed and treated as chronic eczema and later as systemic lupus erythematosus (SLE), delaying the correct diagnosis. The eventual identification of Sézary cells on peripheral smear and confirmatory immunophenotyping established the diagnosis of Sézary syndrome, underscoring the need for a high index of suspicion and a multidisciplinary diagnostic approach when evaluating chronic, treatment-refractory dermatoses.

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