Successful treatment of severe Shulman's syndrome by allogeneic bone marrow transplantation
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu kazuistiky, časopisecké články, práce podpořená grantem
PubMed
9543071
DOI
10.1038/sj.bmt.1701137
Knihovny.cz E-zdroje
- MeSH
- dospělí MeSH
- eozinofilie terapie MeSH
- fasciitida terapie MeSH
- hormony kůry nadledvin terapeutické užití MeSH
- lidé MeSH
- nemoc štěpu proti hostiteli farmakoterapie MeSH
- transplantace kostní dřeně * MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- kazuistiky MeSH
- práce podpořená grantem MeSH
- Názvy látek
- hormony kůry nadledvin MeSH
We describe a patient with severe Shulman's syndrome (ShS) (eosinophilic fasciitis). This auto-immune disease involved not only the skin and muscles, but the bone marrow as well - thereby fulfilling the criteria of severe aplastic anemia. As the disease was steroid-resistant, the patient underwent allogeneic bone marrow transplantation (BMT). Remission of ShS was achieved. Eight months later chronic GVHD developed and relapse of ShS (probably induced by GVHD) occurred. He was successfully treated with corticosteroids and the disappearance of GVHD was followed by cessation of the symptoms of ShS. At present (34 months following BMT) he is doing well and displays no signs of ShS or GVHD. This case suggests that an aggressive immunoablative preparative regimen with subsequent allogeneic BMT can result in long-lasting clinical remission of a severe auto-immune disease.
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