Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare primary cutaneous lymphoma derived from cytotoxic αβ T cells, clinically and histopathologically resembling inflammatory diseases of adipose tissue, particularly lupus panniculitis. It accounts for <1% of all non-Hodgkin's lymphomas, with approximately 20% of cases occurring in children. The main aim of this paper was to present two pediatric cases of SPTCL, highlighting the diagnostic challenges involved. The first patient, a 5-year-9-month-old boy, was admitted with a 15 cm infiltrative lesion on the left thigh, previously misdiagnosed and unsuccessfully treated with antibiotics. Imaging revealed an infiltrate resembling lymphedema. A biopsy confirmed SPTCL with a typical immunophenotype. The patient received EURO-LB 02 protocol therapy for peripheral T-cell lymphoma, complicated by pancytopenia, respiratory infection, and polyneuropathy. Post-treatment follow-up showed lesion regression, with residual subcutaneous atrophy (5 cm). The second patient, a 7-year-old girl, presented with a 10 cm inflammatory lesion on the left thigh and systemic symptoms. Imaging and histopathology confirmed the diagnosis. She was treated with the same protocol. Three years later, disease recurrence occurred on the left forearm, managed with alemtuzumab and methotrexate. Both patients remain under outpatient follow-up. Despite its rarity, SPTCL poses a significant diagnostic challenge in children. Accurate differentiation and early diagnosis are crucial for prompt and effective treatment.
Mitura-Lesiuk et al. (Fri,) studied this question.
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