Diagnostic Approach to Adult Erythroderma: A Rare Case of Sezary Syndrome
This patient presented with Sezary Syndrome, exhibiting atypical dermatologic manifestations that must be differentiated from other causes of erythroderma. This case highlights the importance of a comprehensive diagnostic approach, including clinical evaluation, laboratory tests, imaging, and biopsies. Sezary Syndrome is an inherently aggressive malignancy, characterized by a poor response to treatment and a low 5-year survival rate.
Authors
- Muhammad Noor Diansyah (ORCID: https://orcid.org/0000-0002-5949-432X)
- Quri Meihaerani Savitri (ORCID: https://orcid.org/0000-0003-3493-4082)
- Ami Ashariati (ORCID: https://orcid.org/0000-0003-0508-4496)
- Siprianus Ugroseno Yudho Bintoro (ORCID: https://orcid.org/0000-0003-1360-5298)
- Pradana Zaky Romadhon (ORCID: https://orcid.org/0000-0001-9306-5425)
- Linda Astari
- Merlyna Savitri (ORCID: https://orcid.org/0009-0006-2548-0065)
- Amira Suryani Rahmatika
- Putu Niken Ayu Amrita (ORCID: https://orcid.org/0000-0001-7069-7112)
- Fitria Rettobyan
Institutions
- Universitas Airlangga (ID)
- Universitas Dr. Soetomo (ID)
Publication Details
- Journal
- Iranian journal of pathology
- Published
- 2024-10-01
- DOI
- https://doi.org/10.30699/ijp.2024.2022723.3258
- Primary Topic
- Cutaneous lymphoproliferative disorders research
- Type
- article
- Field-Weighted Citation Impact
- 0.00