Clinicopathologic characteristics of cutaneous chronic graft-versus-host diseases: A retrospective study in Korean patients

  • Sun Ji Kim
  • , Jung Min Choi
  • , Jung Eun Kim
  • , Baik Kee Cho
  • , Dong Wook Kim
  • , Hyun Jeong Park

Research output: Contribution to journalArticlepeer-review

30 Scopus citations

Abstract

Background Chronic graft-versus-host disease (cGVHD) is a major complication in long-term survivors of hematopoietic stem cell transplantation (HSCT). Cutaneous manifestations are frequently the presenting features; therefore, the dermatologist needs to be aware of the wide spectrum of cutaneous cGVHD. Methods We retrospectively evaluated patients' characteristics, clinical, and histological features of cutaneous cGVHD and analyzed factors influencing the severity of cutaneous cGVHD in 100 Korean HSCT recipients between January 1, 1995, and December 31, 2007. Results Clinical manifestations of cutaneous cGVHD mainly presented as lichenoid (60.0%), sclerodermoid (12.0%), or erythematous maculopapular (22.0%) patterns. Other less common findings included xerosis, dyspigmentation, acquired ichthyosis, eczema, exfoliative dermatitis, alopecia, erythema multiforme-like or keratosis pilaris-like eruption. Among 100 patients, 46 patients were investigated for nail involvement, and 29 (63.0%) of them were accompanied with nail abnormalities. Histologically, characteristic lichenoid lesions were observed in 53%, sclerodermoid in 9%, and acute/chronic overlap syndrome in 28% of patients. We also discovered that HSCT from female donors to male recipients increased the severity of cutaneous cGVHD. Conclusions We report a large study about cutaneous cGVHD in Asian patients. Cutaneous cGVHD presented with a wide spectrum of clinical and histological manifestations.

Original languageEnglish
Pages (from-to)1386-1392
Number of pages7
JournalInternational Journal of Dermatology
Volume49
Issue number12
DOIs
StatePublished - Dec 2010

Bibliographical note

Funding Information:
The following grant information was disclosed by the authors: National Science and Technology Major Project for investigational new drug: 2018ZX09201-014. Beijing Municipal Science & Technology Commission: Z181100001518005. University of Macau: MYRG2019-00066-FHS.

Funding Information:
The study was supported by the National Science and Technology Major Project for investigational new drug (2018ZX09201-014), the Beijing Municipal Science & Technology Commission (No. Z181100001518005), and the University of Macau (MYRG2019-00066-FHS). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

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