Hepatoblastoma risk factors: Difference between revisions

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Revision as of 14:31, 5 November 2015

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];Associate Editor(s)-in-Chief: Nawal Muazam M.D.[2]

The table below lists risk factors for hepatoblastoma:^[1]


Associated Disorder	Clinical findings

Aicardi syndrome	Agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms, with a characteristic facies.
Beckwith-Wiedemann syndrome	Hemihypertrophy, hemihyperplasia.
Familial adenomatous polyposis
Glycogen storage diseases I–IV	Symptoms vary by individual disorder.
Low-birth-weight infants	Preterm and small-for-gestation-age neonates.
Simpson-Golabi-Behmel syndrome	Macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of Wilms tumor.
Trisomy 18, other trisomies	Trisomy 18: Microcephaly and micrognathia, clenched fists with overlapping fingers, and failure to thrive. Most patients (>90%) die in the first month of life.

↑ ^1.0 ^1.1 Risk factors. National Cancer Institute 2015. http://www.cancer.gov/types/liver/hp/child-liver-treatment-pdq#link/_570_toc. Accessed on October 28, 2015

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 {{CMG}};{{AE}} {{NM}}
 ==Overview==
+Common risk factors in the development of hepatoblastoma are [[Aicardi syndrome]], [[Beckwith-Wiedemann syndrome]], [[Familial adenomatous polyposis]], [[low birth weight|low birth weight infants]] and [[glycogen storage diseases]].<ref name=risk>Risk factors. National Cancer Institute 2015. http://www.cancer.gov/types/liver/hp/child-liver-treatment-pdq#link/_570_toc. Accessed on October 28, 2015</ref>
 ==Risk Factors==
 The table below lists risk factors for hepatoblastoma:<ref name=risk>Risk factors. National Cancer Institute 2015. http://www.cancer.gov/types/liver/hp/child-liver-treatment-pdq#link/_570_toc. Accessed on October 28, 2015</ref>