Hepatoblastoma risk factors

Hepatoblastoma Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Epidemiology and Demographics
Risk Factors
Screening
Differentiating Hepatoblastoma from other Diseases
Natural History, Complications and Prognosis
Diagnosis
Staging
History and Symptoms
Physical Examination
Laboratory Findings
X Ray
CT
MRI
Ultrasound
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Surgery
Primary Prevention
Secondary Prevention
Cost-Effectiveness of Therapy
Future or Investigational Therapies
Case Studies
Case #1
Hepatoblastoma risk factors On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Hepatoblastoma risk factors All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Hepatoblastoma risk factors
CDC on Hepatoblastoma risk factors
Hepatoblastoma risk factors in the news
Blogs on Hepatoblastoma risk factors
Directions to Hospitals Treating Hepatoblastoma
Risk calculators and risk factors for Hepatoblastoma risk factors

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

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:

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

Template:WikiDoc Sources