Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2016 Nov 3;128(18):2270-2272.
doi: 10.1182/blood-2016-08-732610. Epub 2016 Sep 12.

Acute myeloid leukemia with TP53 germ line mutations

Affiliations
Case Reports

Acute myeloid leukemia with TP53 germ line mutations

Armin Zebisch et al. Blood. .
No abstract available

PubMed Disclaimer

Figures

Figure 1
Figure 1
An LFS pedigree showing for the first time familial clustering of AML. The index patient developed tAML (II:4) following cytotoxic treatment of diverse antecedent malignancies, and the index patient’s father (I:2) developed sAML following myelodysplasia. Filled symbols, subjects with malignancies; asterisk denotes a TP53 c.467G>C, p.R156P germ line mutation carrier; the “minus” denotes a wild-type TP53 germ line status. Numbers in brackets indicate age at diagnosis in years. BC, breast cancer; CML, chronic myeloid leukemia; CRC, colorectal cancer; PNET, primitive neuroectodermal tumor; TC, thyroid carcinoma.

References

    1. West AH, Godley LA, Churpek JE. Familial myelodysplastic syndrome/acute leukemia syndromes: a review and utility for translational investigations. Ann N Y Acad Sci. 2014;1310:111–118. - PMC - PubMed
    1. Arber DA, Orazi A, Hasserjian R, et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood. 2016;127(20):2391–2405. - PubMed
    1. Bougeard G, Renaux-Petel M, Flaman JM, et al. Revisiting Li-Fraumeni Syndrome from TP53 mutation carriers. J Clin Oncol. 2015;33(21):2345–2352. - PubMed
    1. Schulz E, Valentin A, Ulz P, et al. Germline mutations in the DNA damage response genes BRCA1, BRCA2, BARD1 and TP53 in patients with therapy related myeloid neoplasms. J Med Genet. 2012;49(7):422–428. - PubMed
    1. Wölfler A, Erkeland SJ, Bodner C, et al. A functional single-nucleotide polymorphism of the G-CSF receptor gene predisposes individuals to high-risk myelodysplastic syndrome. Blood. 2005;105(9):3731–3736. - PubMed

Substances