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Published on: May 26, 2023
Systemic corticosteroids for subcutaneous panniculitis-like T-cell lymphoma.
E Guenova1, S Schanz, W Hoetzenecker
1Department of Dermatology, University Hospital Zurich, Gloriastraße 31, Zürich, Switzerland; Department of Dermatology, University of Tübingen, Liebermeisterstrasse 25, 72076, Tübingen, Germany.
Systemic corticosteroids effectively treated subcutaneous panniculitis-like T-cell lymphoma (SPTCL). Most patients achieved complete remission, suggesting this as a potential first-line therapy for SPTCL.
Area of Science:
- Dermatology
- Oncology
- Hematology
Background:
- Primary cutaneous γ/δ T-cell lymphoma (PCGD-TCL) is aggressive, unlike subcutaneous panniculitis-like T-cell lymphoma (SPTCL).
- SPTCL, characterized by the α/β T-cell receptor phenotype, typically follows an indolent course with a favorable prognosis.
- Historically, PCGD-TCL and SPTCL were misclassified, leading to aggressive chemotherapy for both, despite SPTCL's less aggressive nature.
Purpose of the Study:
- To evaluate the efficacy of systemic corticosteroids as a treatment for SPTCL.
- To determine the clinical response rate of SPTCL to corticosteroid monotherapy.
Main Methods:
- Retrospective cross-sectional study design.
- Utilized a patient data repository spanning 13 years from two tertiary care university hospitals in Switzerland and Germany.
- Focused on patients diagnosed with SPTCL.
Main Results:
- Treatment with systemic corticosteroids resulted in a complete remission in 80% of SPTCL patients (4 out of 5).
- Demonstrated a high response rate to corticosteroid therapy in the studied SPTCL cohort.
Conclusions:
- Systemic corticosteroids represent a potentially excellent first-line monotherapy for SPTCL.
- Conservative treatment with corticosteroids may be a viable and effective option for managing SPTCL, avoiding more aggressive treatments.
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