Skin ulcers related to chronic graft‐versus‐host disease: clinical findings and associated morbidity. (24th June 2014)

• Record Type: Journal Article
• Authors: Jachiet, M.; de Masson, A.; Peffault de Latour, R.; Rybojad, M.; Robin, M.; Bourhis, J.‐H.; Xhaard, A.; Dhedin, N.; Sicre de Fontbrune, F.; Suarez, F.; Barete, S.; Parquet, N.; Nguyen, S.; Ades, L.; Rubio, M.‐T.; Wittnebel, S.; Bagot, M.; Socié, G.; Bouaziz, J.‐D.
• Is Part Of: British journal of dermatology. Volume 171:Number 1(2014:Jul.)
• Page Start: 63
• Page End: 68
• Publication Date: 2014-06-24
• Subjects: Dermatology -- Periodicals; Skin -- Diseases -- Periodicals; 616.5
• DOI: 10.1111/bjd.12828
• Languages: English
• ISSNs: 0007-0963

Abstract

<abstract abstract-type="main" id="bjd12828-abs-0001"> <title>Summary</title> <sec id="bjd12828-sec-0001" sec-type="section"> <title>Background</title> <p>According to the National Institutes of Health classification of chronic graft‐versus‐host disease (cGVHD), skin ulcers after allogeneic haematopoietic stem‐cell transplantation (HSCT) are recorded as having the maximal severity score but published data are scarce.</p> </sec> <sec id="bjd12828-sec-0002" sec-type="section"> <title>Objectives</title> <p>To describe skin ulcers related to cGVHD with an emphasis on clinical findings, associated morbidity, management and evolution.</p> </sec> <sec id="bjd12828-sec-0003" sec-type="section"> <title>Patients and methods</title> <p>A multicentre retrospective analysis was carried out of patients with a diagnosis of cGVHD skin ulcers.</p> </sec> <sec id="bjd12828-sec-0004" sec-type="section"> <title>Results</title> <p>All 25 patients included in the study had sclerotic skin cGVHD and 21 had lichenoid skin lesions associated with the sclerotic skin lesions. Thirteen patients had severe cGVHD without considering the skin, because of the involvement of an extracutaneous organ by cGVHD. The median time from HSCT to the onset of ulcers was 44 months. In addition to scleroderma, initial skin lesions at the site of ulcers were bullous erosive lichen in 21 patients and bullous erosive morphoea in four patients. Fifteen patients had an inaugural oedema. Ulcers were mostly bilateral with a predilection for the lower limbs. They were frequently colonized but few infections occurred. Four patients died during a median follow‐up period of 55 months.</p> </sec> <sec id="bjd12828-sec-0005" sec-type="section"> <title>Conclusions</title> <p>Chronic graft‐versus‐host disease skin ulcers occur in patients with sclerodermatous skin cGVHD, are associated with severe cGVHD, often start with bullous lichenoid lesions or bullous morphoea and seem to cause more morbidity than mortality, given the low rate of mortality observed in our series of patients.</p> </sec> </abstract>