Diagnostic Conundrums of T-CLPDs: A Case Report of a CD4-Positive T-LGLL with Overlapping Morphological Features of T-PLL
摘要
T-Large Granular Lymphocytic Leukemia (T-LGLL) and T-cell prolymphocytic leukemia (T-PLL) are rare forms of chronic lymphoproliferative disorders (CLPDs) with distinct clinical and morphological features. However, cases with overlapping clinical and morphological features pose a diagnostic challenge. Here, we report a case of a 57-year-old male with an indolent clinical course, high total leukocyte count, and atypical lymphoid cells with granular cytoplasm and prolymphocytoid nuclei on peripheral blood smear and intra-sinusoidal infiltration on trephine biopsy. Immunophenotypic analysis revealed CD4 positivity and loss of CD5 and CD7 expression. Despite overlapping features, a diagnosis of CD4-positive T-LGLL was made based on the overall clinical presentation, morphological features, and immunophenotypic profile.