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Yellow nail syndrome after allogeneic haematopoietic stem cell transplantation in two patients with multiple myeloma.
Gregoire, Céline; Guiot, Julien; Vertenoeil, Gaëlle; Willems, Évelyne; Hafraoui, Kaoutar; Corhay, Jean-Louis; Louis, Renaud; Beguin, Yves.
Afiliación
  • Gregoire C; a Department of Medicine, Division of Hematology , CHU of Liège and University of Liège , Liège , Belgium.
  • Guiot J; b Department of Medicine, Division of Pneumology , CHU of Liège and University of Liège , Liège , Belgium.
  • Vertenoeil G; a Department of Medicine, Division of Hematology , CHU of Liège and University of Liège , Liège , Belgium.
  • Willems É; a Department of Medicine, Division of Hematology , CHU of Liège and University of Liège , Liège , Belgium.
  • Hafraoui K; a Department of Medicine, Division of Hematology , CHU of Liège and University of Liège , Liège , Belgium.
  • Corhay JL; b Department of Medicine, Division of Pneumology , CHU of Liège and University of Liège , Liège , Belgium.
  • Louis R; b Department of Medicine, Division of Pneumology , CHU of Liège and University of Liège , Liège , Belgium.
  • Beguin Y; a Department of Medicine, Division of Hematology , CHU of Liège and University of Liège , Liège , Belgium.
Acta Clin Belg ; 71(6): 428-430, 2016 Dec.
Article en En | MEDLINE | ID: mdl-27075800
OBJECTIVE AND IMPORTANCE: Yellow nail syndrome (YNS) is a rare disorder of unknown aetiology characterized by the triad of yellow nails, lymphoedema and respiratory manifestations. About 200 cases have been reported, but a lot of patients probably elude proper diagnosis because of both variability of symptoms and ignorance of this syndrome by many physicians. The pathogenesis remains unclear, and could involve functional lymphatic abnormalities, microvasculopathy or lymphocyte deficiency, but none of these hypotheses seems fully satisfactory. CLINICAL PRESENTATION: We report for the first time two cases of YNS associated with multiple myeloma relapsing after non-myeloablative haematopoietic cell transplantation (HCT). In these two cases, onset or worsening of YNS symptoms followed graft-versus-host disease (GvHD) manifestations. INTERVENTION: Corticosteroids given to treat GvHD also improved YNS manifestations. CONCLUSION: YNS after HCT might be a microvascular manifestation of endothelial GvHD and corticosteroids might be an effective treatment.
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Síndrome de la Uña Amarilla / Enfermedad Injerto contra Huésped / Mieloma Múltiple Tipo de estudio: Diagnostic_studies Límite: Adult / Humans / Male / Middle aged Idioma: En Revista: Acta Clin Belg Año: 2016 Tipo del documento: Article País de afiliación: Bélgica
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Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trasplante de Células Madre Hematopoyéticas / Síndrome de la Uña Amarilla / Enfermedad Injerto contra Huésped / Mieloma Múltiple Tipo de estudio: Diagnostic_studies Límite: Adult / Humans / Male / Middle aged Idioma: En Revista: Acta Clin Belg Año: 2016 Tipo del documento: Article País de afiliación: Bélgica