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Germline TP53 c.566C>T mutation incidentally diagnosed during treatment for acute myeloid leukaemia: A case report
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  • Hiroshi Sato,
  • Seiki Matsuo,
  • Yukiko Ando,
  • Yuko Imamura,
  • Masaya Hirose
Hiroshi Sato
Hyogo Prefectural Amagasaki General Medical Center

Corresponding Author:[email protected]

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Seiki Matsuo
Hyogo Prefectural Amagasaki General Medical Center
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Yukiko Ando
Hyogo Prefectural Amagasaki General Medical Center
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Yuko Imamura
Hyogo Prefectural Amagasaki General Medical Center
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Masaya Hirose
Hyogo Prefectural Amagasaki General Medical Center
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Abstract

A 53-year-old woman was admitted at our hospital for the treatment of acute myeloid leukaemia. Heterozygous c.566C>T mutation in the TP53 gene was found in leukaemia cells and germline cells. The number of germline mutation found incidentally will increase. Therefore, patients with such incidental findings must undergo adequate genetic counselling.
25 Oct 2021Submitted to Clinical Case Reports
27 Oct 2021Submission Checks Completed
27 Oct 2021Assigned to Editor
03 Nov 2021Reviewer(s) Assigned
22 Nov 2021Review(s) Completed, Editorial Evaluation Pending
22 Nov 2021Editorial Decision: Revise Minor
23 Nov 20211st Revision Received
24 Nov 2021Submission Checks Completed
24 Nov 2021Assigned to Editor
24 Nov 2021Review(s) Completed, Editorial Evaluation Pending
03 Dec 2021Editorial Decision: Accept