| Literature DB >> 30542432 |
Guan-Nan Wang1, Yong Cui2, Wu-Gan Zhao1, Ling Li3, Xu-Dong Zhang3, Yu Chang3, Xian-Zheng Gao1, Ye Li1, Ming-Zhi Zhang3, Wen-Cai Li1.
Abstract
Hydroa vacciniforme-like lymphoproliferative disorder (HVLPD) is defined as a distinctive clinicopathological type of cutaneous lymphoma and a subset of patients with this disease exhibit the natural killer (NK)-cell phenotype. The HVLPD-NK cell phenotype may be difficult to distinguish from cutaneous natural killer T-cell lymphoma (CNKTL), as these two diseases share similar immunophenotypic markers. Therefore, the aim of the present study was to analyze the clinicopathological features of this rare disease and compare these features with those of CNKTL. The clinical, histopathological and molecular features of 5 patients with the HVLPD-NK cell phenotype and 11 patients with CNKTL were evaluated. As well as certain subtle histopathological differences, there marked differences the age, distribution of lesions and clinical course differed between patients with these two diseases. These results suggest that the HVLPD-NK cell phenotype should be classified as a separate disorder and treated accordingly.Entities:
Keywords: Epstein-Barr virus; cluster of differentiation 56; cutaneous T cell lymphoma; differential diagnosis; hydroa vacciniforme-like lymphoproliferative disorder; natural killer T-cell lymphoma
Year: 2018 PMID: 30542432 PMCID: PMC6257548 DOI: 10.3892/etm.2018.6768
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447