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Tacrolimus in Gastrointestinal Bleeding in a Young Boy With Hereditary Hemorrhagic Telangiectasia.
Pruijsen, Jessica M; Kroon, Steven; Mager, Johannes J; Bungener, Laura B; van der Doef, Hubert P J.
Afiliação
  • Pruijsen JM; From the Pediatric Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • Kroon S; Department of Pulmonology, St. Antonius Hospital Nieuwegein, The Netherlands.
  • Mager JJ; Department of Pulmonology, St. Antonius Hospital Nieuwegein, The Netherlands.
  • Bungener LB; Department of Laboratory Medicine, Transplantation Immunology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
  • van der Doef HPJ; From the Pediatric Gastroenterology and Hepatology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
JPGN Rep ; 2(4): e133, 2021 Nov.
Article em En | MEDLINE | ID: mdl-37206467
ABSTRACT
Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease in which gastrointestinal bleeding is a rare presenting symptom in children. Gastrointestinal bleeding in children is treated locally by endoscopy. When a focus of bleeding cannot be reached by endoscopy, management of these patients can be challenging. Previous reports showed a favorable outcome of treatment with tacrolimus in an adult HHT patient with liver vascular malformations and epistaxis and in a HHT patient with pulmonary hypertension. We report the first pediatric HHT patient who benefited from tacrolimus treatment. Our case demonstrated a remarkable decline in blood transfusions and better quality of life during the period of tacrolimus treatment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Aspecto: Patient_preference Idioma: En Revista: JPGN Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Aspecto: Patient_preference Idioma: En Revista: JPGN Rep Ano de publicação: 2021 Tipo de documento: Article