Hepatoblastoma risk factors: Difference between revisions

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Revision as of 13:39, 28 October 2015

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

Overview

Risk Factors

Being male.

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.

References

↑ 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

Template:WikiDoc Sources

[risk-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

[1]

@@ Line 4: / Line 4: @@
 ==Overview==
 ==Risk Factors==
-Risk factors for hepatoblastoma including the following:
 * Being male.
-* Having [[familial adenomatous polyposis]] (FAP).
-* Having [[Beckwith-Wiedemann syndrome]].
-* Having had a very low weight at birth.
 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>
@@ Line 22: / Line 16: @@
 |-
-| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Aicardi syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;" |
+| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''[[Aicardi syndrome]]'''|| style="padding: 5px 5px; background: #F5F5F5;" |
 :* Agenesis of the corpus callosum, chorioretinal lacunae, and infantile spasms, with a characteristic facies.
 |-
-| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Beckwith-Wiedemann syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;"|
+| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''[[Beckwith-Wiedemann syndrome]]'''|| style="padding: 5px 5px; background: #F5F5F5;"|
 :* Hemihypertrophy, hemihyperplasia.
 |-
-| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Familial adenomatous polyposis'''|| style="padding: 5px 5px; background: #F5F5F5;"|
+| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''[[Familial adenomatous polyposis]]'''|| style="padding: 5px 5px; background: #F5F5F5;"|
 :*
 |-
-| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Glycogen storage diseases I–IV '''|| style="padding: 5px 5px; background: #F5F5F5;" |
+| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''[[Glycogen storage diseases]] I–IV '''|| style="padding: 5px 5px; background: #F5F5F5;" |
 :*Symptoms vary by individual disorder.
@@ Line 46: / Line 40: @@
 |-
-| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Simpson-Golabi-Behmel syndrome'''|| style="padding: 5px 5px; background: #F5F5F5;"|
+| style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''[[Simpson-Golabi-Behmel syndrome]]'''|| style="padding: 5px 5px; background: #F5F5F5;"|
-:*Macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of Wilms tumor.
+:*Macroglossia, macrosomia, renal and skeletal abnormalities, and increased risk of [[Wilms tumor]].
 |-
 |style="padding: 5px 5px; background: #DCDCDC; font-weight: bold" align=center | '''Trisomy 18, other trisomies'''|| style="padding: 5px 5px; background: #F5F5F5;" |
-:*Trisomy 18: Microcephaly and micrognathia, clenched fists with overlapping fingers, and failure to thrive. Most patients (>90%) die in the first month of life.
+:*[[Trisomy 18]]: [[Microcephaly]] and [[micrognathia]], clenched fists with overlapping fingers, and failure to thrive. Most patients (>90%) die in the first month of life.
 |}
 ==References==
-{{reflist|2}}
+{{reflist|1}}
 [[Category:Disease]]

Hepatoblastoma risk factors: Difference between revisions

Revision as of 13:39, 28 October 2015

Overview

Risk Factors

References

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