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Subcutaneous panniculitis-like T cell lymphoma presented as erythema nodosum: A case report

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DERMATOLOGIC THERAPY
卷 34, 期 1, 页码 -

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WILEY
DOI: 10.1111/dth.14572

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erythema nodosum; IFNα phenotype; subcutaneous panniculitis‐ like T cell lymphoma

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SPTCL is an extremely rare subtype of primary cutaneous T cell lymphomas, presenting with subcutaneous nodules and often leading to misdiagnosis. Treatment with recombinant human interferon alpha-1b showed effectiveness in this case, with lesions gradually regressing and no new nodules appearing during a 10-month follow-up.
Subcutaneous panniculitis-like T cell lymphoma (SPTCL) is an extremely rare subtype of primary cutaneous T cell lymphomas mimicking panniculitis. Clinically, patients are usually presented with subcutaneous nodules, which usually leads to initial misdiagnosis as a benign cutaneous condition. Here, we report a 40-year-old female who presented with subcutaneous erythematous nodules on her extremities with fever. On the basis of the clinical presentations, histopathological features and immunohistochemical findings, a diagnosis of SPTCL was made. The patient was treated with the injection of recombinant human interferon alpha-1b (30 mu g) every other day for 3 months. The lesions gradually regressed. No new erythema nodules reappeared during the 10-month follow-up.

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