Hepatoblastoma risk factors: Difference between revisions

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Revision as of 22:53, 13 November 2015

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

Overview

Common risk factors in the development of hepatoblastoma are Aicardi syndrome, Beckwith-Wiedemann syndrome, familial adenomatous polyposis, low birth weight infants, and glycogen storage diseases.^[1]

Risk Factors

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	Adenoma, hepatoblastoma
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

↑ ^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

Template:WikiDoc Sources

[risk-1] 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

[1]

@@ Line 17: / Line 17: @@
 | 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.
+:* 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;"|
-:* Hemihypertrophy, hemihyperplasia.
+:* [[Hemihypertrophy]], hemihyperplasia.
 |-
@@ Line 41: / Line 41: @@
 | 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.
 |}

Hepatoblastoma risk factors: Difference between revisions

Revision as of 22:53, 13 November 2015

Overview

Risk Factors

References

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