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Successful treatment of congenital erythropoietic porphyria using matched unrelated hematopoietic stem cell transplantation in an adult: A case report.
Peterlin, Pierre; Bonnelye, Julia; Garnier, Alice; Le Bourgeois, Amandine; Guillaume, Thierry; Jullien, Maxime; Dutartre, Hervé; Le Moigne, Marie; Schmitt, Caroline; Gouya, Laurent; Poli, Antoine; Barbarot, Sebastien; Chevallier, Patrice.
Afiliação
  • Peterlin P; Clinical Hematology Nantes University Hospital Nantes France.
  • Bonnelye J; Equipe 12 CRCI2NA - INSERM UMR1307 CNRS UMR 6075 CRCINA IRS-UN University of Nantes Nantes France.
  • Garnier A; Dermatology Department Reference Center for Cutaneous Porphyrias Nantes University Hospital Nantes France.
  • Le Bourgeois A; Clinical Hematology Nantes University Hospital Nantes France.
  • Guillaume T; Clinical Hematology Nantes University Hospital Nantes France.
  • Jullien M; Clinical Hematology Nantes University Hospital Nantes France.
  • Dutartre H; Equipe 12 CRCI2NA - INSERM UMR1307 CNRS UMR 6075 CRCINA IRS-UN University of Nantes Nantes France.
  • Le Moigne M; Clinical Hematology Nantes University Hospital Nantes France.
  • Schmitt C; Dermatology Department Reference Center for Cutaneous Porphyrias Nantes University Hospital Nantes France.
  • Gouya L; Dermatology Department Reference Center for Cutaneous Porphyrias Nantes University Hospital Nantes France.
  • Poli A; Reference Center for Rare Diseases Porphyrias Louis Mourier Hospital AP-HP, Colombes and Research Center of Inflammation UMR1149 INSERM Université de Paris Paris France.
  • Barbarot S; Reference Center for Rare Diseases Porphyrias Louis Mourier Hospital AP-HP, Colombes and Research Center of Inflammation UMR1149 INSERM Université de Paris Paris France.
  • Chevallier P; Reference Center for Rare Diseases Porphyrias Louis Mourier Hospital AP-HP, Colombes and Research Center of Inflammation UMR1149 INSERM Université de Paris Paris France.
Skin Health Dis ; 4(2): e342, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38577034
ABSTRACT
Congenital erythropoietic porphyria (CEP), or Gunther disease, is a rare genetic disease responsible for severe dermatologic, hepatic and/or haematological damages related to the deficient activity of the uroporphyrinogen III synthase. Allogeneic stem cell transplantation (Allo-SCT) represents the only curative treatment and few allotransplanted cases have been reported in children but not in adults. Here we report for the first time the successful cure of a 46-year old man with CEP with a 5-year follow-up after Allo-SCT.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Skin Health Dis Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Skin Health Dis Ano de publicação: 2024 Tipo de documento: Article