Abstract
Cutaneous lymphoid infiltrates in children pose a diagnostic challenge because reactive lymphoid processes and low-grade lymphoproliferative disorders can share overlapping clinical, histopathologic, and molecular features. We report a case of a two-year-old child presenting with a persistent erythematous plaque on the right cheek following a presumed mosquito bite. The lesion was refractory to topical antibiotics and corticosteroids. Histopathologic examination revealed a dense CD4⁺ T-cell-predominant dermal infiltrate, and molecular studies demonstrated both beta and gamma T-cell receptor (TCR) clonality. Although the findings were histopathologically compatible with primary cutaneous CD4⁺ small/medium T-cell lymphoproliferative disorder (PCSM-TCLPD), the patient’s age, clinical context, and subsequent clinical course suggested an atypical clonal reactive T-cell process. Following a diagnostic biopsy, the lesion demonstrated partial clinical regression. A conservative management strategy with clinical observation and serial photography was adopted, avoiding unnecessary systemic therapy. This case highlights the diagnostic gray zone between clonal reactive lymphoid proliferations and PCSM-TCLPD in very young children, an age group in which such presentations are exceedingly rare, and emphasizes the importance of clinicopathologic correlation, multidisciplinary evaluation, and cautious management. It also raises awareness that these entities may exist along a biological spectrum rather than representing entirely distinct processes.