Clinical characteristics and disease course in black patients with lymphomatoid papulosis: A case series

Shamir Geller*, Sarah J. Noor, Patricia L. Myskowski

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Introduction: Lymphomatoid papulosis (LyP) is a CD30+ T-cell lymphoproliferative disorder (LPD) presenting as a recurrent eruption of papules and nodules which resolve spontaneously. CD30+ LPD prevalence in African American (AA)/Black patients is lower compared to White patients. CD30+ LPD has been recently reported to have worse outcomes in AA patients compared to White patients. Methods: A retrospective chart review identified eight AA patients with LyP. We describe our experience with these eight patients and review the literature on similar cases. Results: In half of the eight included patients, lesions occurred 1-4 years before they were diagnosed. In six patients (75%), resolution of the lesions resulted in hyperpigmented macules and scars. Five patients (63%) had also mycosis fungoides. Most of the patients who were followed (4/7, 57%) did not have complete resolution at their last visit, despite different treatment approaches. Discussion: Our results highlight that although LyP has an indolent course in AA/Black patients, residual hyperpigmentation and scars frequently occur, highlighting the need for better treatments of this lymphoproliferative disorder in this specific population.

Original languageEnglish
Pages (from-to)89-91
Number of pages3
JournalJournal of Drugs in Dermatology
Volume19
Issue number1
DOIs
StatePublished - Jan 2020
Externally publishedYes

Fingerprint

Dive into the research topics of 'Clinical characteristics and disease course in black patients with lymphomatoid papulosis: A case series'. Together they form a unique fingerprint.

Cite this