Clinicopathological analysis of primary cutaneous CD4‐positive small/medium pleomorphic T‐cell lymphoproliferative disorder: a retrospective study of 22 patients

Abstract Background Primary cutaneous CD4‐positive small/medium pleomorphic T‐cell lymphoproliferative disorder has been defined as a type of lymphoproliferative disorder with indolent clinical course and excellent prognosis, yet a precise diagnosis is still hard to reach. Methods A retrospective analysis of 22 patients including 16 females and six males was performed. Results The age of patients ranged from 5 to 79 years. The average age of all patients was 43.5, and the median age of all patients was 44.5. Two patients had multiple lesions, and others were presented with a solitary asymptomatic lesion. Besides general features, folliculotropism was observed in four cases. In addition to express CD3 and CD4, CD30 were positive to some extent. Some reactive cells could express CD8 and CD20. For follicular helper T‐cell markers, although CXCL‐13 was negative in the stained cases (18/18), the expression of PD‐1 (12/17), BCL‐6 (12/16) and CD10 (11/15) was observed in most cases. In addition, we performed T‐cell receptor (TCR) rearrangement on five patients, and all of them showed monoclonality. Nearly all patients had excellent prognosis. Conclusions Primary cutaneous CD4‐positive small/medium pleomorphic T‐cell lymphoproliferative disorder is complex. Some features like folliculotropism should also be noted. Besides, the expression of follicular helper T‐cell markers is not invariable. Moreover, CD8 positivity, Ki‐67 index, and lesion number were perhaps not absolute prognostic indicators. To reach a diagnosis of this rare entity, putting all the pieces together is important.