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Severe graft-versus-host disease post allogeneic hematopoietic stem cell transplantation due to loss of HLA heterozygosity in recipient lymphocytes after full graft rejection.
Xue, Song; Miao, Lili; Gong, Zimu; Huang, Wenqiu; Zhang, Yongping; Liu, Fuhong; Wang, Jingbo.
Afiliação
  • Xue S; Department of Hematology, Aerospace Center Hospital Peking University Aerospace School of Clinical Medicine Beijing China.
  • Miao L; Beijing Bo Fu Rui Gene Diagnostics Co., Ltd Beijing China.
  • Gong Z; Cancer Center, Houston Methodist Hospital Houston Texas USA.
  • Huang W; Department of Hematology, Aerospace Center Hospital Peking University Aerospace School of Clinical Medicine Beijing China.
  • Zhang Y; Department of Hematology, Aerospace Center Hospital Peking University Aerospace School of Clinical Medicine Beijing China.
  • Liu F; Department of Hematology, Aerospace Center Hospital Peking University Aerospace School of Clinical Medicine Beijing China.
  • Wang J; Department of Hematology, Aerospace Center Hospital Peking University Aerospace School of Clinical Medicine Beijing China.
Cancer Innov ; 2(4): 312-317, 2023 Aug.
Article em En | MEDLINE | ID: mdl-38089744
ABSTRACT
Germ cell tumors complicated by hematological malignancy (HM) are a rare clinical phenomenon. Allogeneic hematopoietic stem cell transplantation (allo-HSCT) is a potentially effective therapy, but graft-versus-host disease (GVHD) is a life-threatening complication. We report a case of a 13-year-old female patient diagnosed with germ cell tumors followed by acute lymphoblastic leukemia. After chemotherapy, she received allo-HSCT and her chimerism rate decreased rapidly to near zero by 6 months without evidence of HM recurrence. However, she developed severe, multiorgan GVHD-like manifestations. DNA analysis revealed the pathogenesis of GVHD to be loss of HLA heterozygosity in recipient hematopoietic cells.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article