Stage IV cutaneous acute graft-versus-host disease. Clinical and histological study of 15 cases
Autor: | Yolanda Delgado-Jiménez, Amaro García-Díez, Pablo F. Peñas, Rebeca Goiriz, Javier Fraga, Maximiliano Aragüés, Á Figuera, Jesús Fernández-Herrera, S. Pérez-Gala |
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Rok vydání: | 2009 |
Předmět: |
medicine.medical_specialty
Pathology integumentary system business.industry Mortality rate Retrospective cohort study Dermatology medicine.disease Gastroenterology Toxic epidermal necrolysis Transplantation Basal (phylogenetics) Infectious Diseases Internal medicine medicine Stage (cooking) business Complication Cause of death |
Zdroj: | Journal of the European Academy of Dermatology and Venereology. 23:1398-1404 |
ISSN: | 0926-9959 |
Popis: | Background The most severe form of cutaneous acute graft-versus-host disease (aGVHD), stage IV, is characterized by the appearance of vesicles and blisters. Objective To describe the clinicopathological characteristics and evolution of stage IV cutaneous aGVHD presented in our hospital. Method Retrospective study. The following criteria for inclusion were applied: (i) patients subjected to allogeneic stem cell transplantation between 1st January 1984 and 31st of December 2006; (ii) development of vesicles and/or blisters; (iii) extracutaneous coincidental aGVHD manifestations; and (iv) presence of histopathological features consistent with aGVHD. Results Fifteen cases (10 females and 5 males) were studied. The mean age was 38.1 years. The lesions appeared after a median interval of 19 days, always following a milder stage of GVHD. Two patterns of clinical evolution were found. Mucosal involvement was observed in nine patients. Nikolsky's sign was positive in eight patients. Nine of the patients had biopsies of the vesiculobullous stage which showed a subepidermal blister with epidermal necrosis and basal vacuolar degeneration. Only two patients survived. Conclusion Stage IV cutaneous aGVHD is a severe and unusual complication after haematopoietic stem cell transplantation. Prognosis is poor with a very high mortality rate, although the cause of death is varied and not strictly linked to the cutaneous disease. |
Databáze: | OpenAIRE |
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