The changing approach for identifying hereditary colorectal cancer syndromes

doi:10.1038/s41575-020-0348-y

. 2020 Oct;17(10):593-594.

doi: 10.1038/s41575-020-0348-y.

The changing approach for identifying hereditary colorectal cancer syndromes

Luigi Laghi^{1

2}, Luigi Ricciardiello^{3

4

5}

Affiliations

¹ Department of Medicine and Surgery, University of Parma, Parma, Italy. luigiandreagiuseppe.laghi@unipr.it.
² Laboratory of Molecular Gastroenterology, Humanitas Clinical and Research Centre - IRCCS -, Rozzano, Italy. luigiandreagiuseppe.laghi@unipr.it.
³ Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy. luigi.ricciardiello@unibo.it.
⁴ Center for the Studies of Hereditary Cancers, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy. luigi.ricciardiello@unibo.it.
⁵ Center for Applied Biomedical Research, University of Bologna, Sant'Orsola-Malpighi Hospital, Bologna, Italy. luigi.ricciardiello@unibo.it.

PMID: 32651554
DOI: 10.1038/s41575-020-0348-y

The changing approach for identifying hereditary colorectal cancer syndromes

Luigi Laghi et al. Nat Rev Gastroenterol Hepatol. 2020 Oct.

. 2020 Oct;17(10):593-594.

doi: 10.1038/s41575-020-0348-y.

Authors

Luigi Laghi^{1

2}, Luigi Ricciardiello^{3

4

5}

Affiliations

¹ Department of Medicine and Surgery, University of Parma, Parma, Italy. luigiandreagiuseppe.laghi@unipr.it.
² Laboratory of Molecular Gastroenterology, Humanitas Clinical and Research Centre - IRCCS -, Rozzano, Italy. luigiandreagiuseppe.laghi@unipr.it.
³ Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy. luigi.ricciardiello@unibo.it.
⁴ Center for the Studies of Hereditary Cancers, Department of Medical and Surgical Sciences, University of Bologna, Bologna, Italy. luigi.ricciardiello@unibo.it.
⁵ Center for Applied Biomedical Research, University of Bologna, Sant'Orsola-Malpighi Hospital, Bologna, Italy. luigi.ricciardiello@unibo.it.

PMID: 32651554
DOI: 10.1038/s41575-020-0348-y

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References

1. Bray, F. et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 68, 394–424 (2018). - DOI
1. Aaltonen, L. A. et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N. Engl. J. Med. 338, 1481–1487 (1998). - DOI
1. Stoffel, E. M. & Murphy, C. C. Epidemiology and mechanisms of the increasing incidence of colon and rectal cancers in young adults. Gastroenterology 158, 341–353 (2020). - DOI
1. Picó, M. D. et al. Clinical and pathological characterization of Lynch-like syndrome. Clin. Gastroenterol. Hepatol. 18, 368–374 (2020). - DOI
1. Lindor, N. M. et al. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X. J. Am. Med. Assoc. 293, 1979–1985 (2005). - DOI

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[1] Bray, F. et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 68, 394–424 (2018). - DOI

[2] Bray, F. et al. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 68, 394–424 (2018). - DOI

[3] Aaltonen, L. A. et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N. Engl. J. Med. 338, 1481–1487 (1998). - DOI

[4] Aaltonen, L. A. et al. Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N. Engl. J. Med. 338, 1481–1487 (1998). - DOI

[5] Stoffel, E. M. & Murphy, C. C. Epidemiology and mechanisms of the increasing incidence of colon and rectal cancers in young adults. Gastroenterology 158, 341–353 (2020). - DOI

[6] Stoffel, E. M. & Murphy, C. C. Epidemiology and mechanisms of the increasing incidence of colon and rectal cancers in young adults. Gastroenterology 158, 341–353 (2020). - DOI

[7] Picó, M. D. et al. Clinical and pathological characterization of Lynch-like syndrome. Clin. Gastroenterol. Hepatol. 18, 368–374 (2020). - DOI

[8] Picó, M. D. et al. Clinical and pathological characterization of Lynch-like syndrome. Clin. Gastroenterol. Hepatol. 18, 368–374 (2020). - DOI

[9] Lindor, N. M. et al. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X. J. Am. Med. Assoc. 293, 1979–1985 (2005). - DOI

[10] Lindor, N. M. et al. Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: Familial colorectal cancer type X. J. Am. Med. Assoc. 293, 1979–1985 (2005). - DOI

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The changing approach for identifying hereditary colorectal cancer syndromes

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The changing approach for identifying hereditary colorectal cancer syndromes

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