Hydroa vacciniforme‐like lymphoproliferative disorder in an elderly Chinese patient and a literature review of adult cases. (21st June 2018)

• Record Type: Journal Article
• Authors: Long, Valencia; Liang, Michelle W.; Tan, Suat Hoon
• Is Part Of: International journal of dermatology. Volume 57:Number 11(2018)
• Page Start: 1283
• Page End: 1292
• Publication Date: 2018-06-21
• Subjects: Dermatology -- Periodicals; 616.5
• DOI: 10.1111/ijd.14050
• Languages: English
• ISSNs: 0011-9059

Abstract

Abstract: Hydroa vaccinforme‐like lymphoproliferative disorder (HVLPD) is a rare T‐cell lymphoproliferative disorder driven by the Epstein–Barr Virus (EBV). It was initially designated under the 2008 WHO classification of tumors of hematopoietic and lymphoid tissues as a distinct entity but has been recently reclassified as a lymphoproliferative disorder under the 2016 revision of the 2008 WHO classification of lymphoid malignancies. HVLPD mainly affects Asian, Central, and South American children. It is rarely seen in adults. Although HVLPD may initially be limited to cutaneous involvement and run an indolent course, some patients may develop a rapidly aggressive course. We report a case of an elderly Chinese man with cutaneous‐limited disease and a favorable course. A review of adult cases of HVLPD published in the English literature, with comparison to our case, is also presented in this paper.