Oncogenic alterations in KIR3DL1 in cutaneous acral CD8+ lymphoproliferative disorder.
Marion WobseSilke AppenzellerSabine RothClaudia SiedelMatthias GoebelerEva GeissingerAndreas RosenwaldKatja MaurusPublished in: The British journal of dermatology (2024)
Alterations of KIR3DL1 gene may be of pathogenetic relevance for acral CD8+ TLPD. Loss of KIR3DL1 protein expression may support the diagnosis of this indolent lymphoma entity, albeit not being a subtype-specific discriminative feature.