An adult patient with Nijmegen Breakage Syndrome and Hodgkin's lymphoma

Katharina Engel, Martina Rudelius, Felix G. Meinel, Christian Peschel, Ulrich Keller

Publikation: Beitrag in FachzeitschriftArtikelBegutachtung

4 Zitate (Scopus)

Abstract

Background: Nijmegen Breakage Syndrome (NBS) is a rare autosomal recessive DNA repair disorder characterized by immune deficiency, microcephaly, mental retardation and a disposition for the development of hematological malignancies. So far, mostly pediatric patients have been described, since the underlying condition is often fatal before adulthood. Many patients diagnosed with Hodgkin lymphoma (HL) due to this DNA repair defect receive reduced treatment followed by early progression and fatal outcome. Case presentation: We describe here a 26-year old male caucasian patient with NBS who presented with multi organ failure due to HL. Immediate intensive chemotherapy lead to complete remission and reversed organ failure. Conclusion: We show that application of standard chemotherapy can lead to long-term disease free survival in patients with a DNA repair disorder. Furthermore, we describe here, to the best of our knowledge, the first adult patient with NBS and HL.

OriginalspracheEnglisch
Aufsatznummer2
FachzeitschriftBMC Hematology
Jahrgang14
Ausgabenummer1
DOIs
PublikationsstatusVeröffentlicht - 2014

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