Liver mass MRI: Difference between revisions

Jump to navigation Jump to search
Line 16: Line 16:


*Characterization of the dynamics of contrast uptake
*Characterization of the dynamics of contrast uptake
{| class="wikitable"
!
!Ultrasound
!CT scan
!MRI
|-
|Hepato cellular adenoma
|
* Heterogeneous
* Hyperechoic if steatotic
* Anechoic center if hemorrhage
|
* Well demarcated with peripheral enhancement
* Homogenous more often than heterogeneous
* Hypodense if steatotic
* Hyperdense if hemorrhagic
|
* HNF1 α: signal lost on chemical shift; moderate arterial enhancement without persistent enhancement during delayed phase
* IHCA: markedly hyperintense on T2 with stronger signal peripherally; persistent enhancement in delayed phase
* β-Catenin: inflammatory subtype has same appearance as IHCA
** Noninflammatory is heterogeneous with no signal dropout on chemical shift
** Isointense of T1 and T2 with strong arterial enhancement and delayed washout
|-
|Hemangioma
|
* Hyperechoic with well-defined rim and with few intranodular vessels
|
* Discontinuous peripheral nodular enhancement
* Isoattenuating to aorta with progressive centripetal fill-in
|
* T1: hypointense; discontinuous peripheral enhancement with centripetal fill-in
* T2: hyperintense relative to spleen
|-
|FNH
|
* Generally isoechoic
|
* Central scar
* Arterial phase shows homogenous hyperdense lesion
* Returns to precontrast density during portal phase that is hypo or isodense
|
* T1: isointense or slightly hypointense. Gadolinium produces early enhancement with central scar enhancement during delayed phase
* T2: slightly hyperintense or isointense
|-
|NRH
|Isoechoic/hyperechoic
|
* Nonenhancing nodules, sometimes hypodense, with variable sizes (most sub-centimeter)
|
* T1: hyperintense
* T2: varied intensity (hypo/iso/hyperintense)
|-
|
|
|
|
|}
[[Image: Hepatoblastoma-1.jpg|center|thumb|400px]]
[[Image: Hepatoblastoma-1.jpg|center|thumb|400px]]



Revision as of 15:51, 5 February 2018

Liver Mass Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differential Diagnosis

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

Evaluation of Liver Mass

Staging

History and Symptoms

Physical Examination

Laboratory Studies

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Case Studies

Case #1

Liver mass MRI On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Liver mass MRI

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Liver mass MRI

CDC on Liver mass MRI

Liver mass MRI in the news

Blogs on Liver mass MRI

Directions to Hospitals Treating bone or soft tissue mass

Risk calculators and risk factors for Liver mass MRI

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]

Overview

On MRI, characteristic features for the diagnosis of liver mass, include: higher soft tissue contrast, lack of radiation exposure, lesion characterization by evaluation of signal intensities, improving detection of hypervascular lesions, and characterization of the dynamics of contrast uptake.[1]

MRI

On MRI, characteristic features for the diagnosis of liver mass, include:

  • Higher soft tissue contrast
  • Lack of radiation exposure
  • Lesion characterization by evaluation of signal intensities
  • Improving detection of hypervascular lesions
  • Characterization of the dynamics of contrast uptake
Ultrasound CT scan MRI
Hepato cellular adenoma
  • Heterogeneous
  • Hyperechoic if steatotic
  • Anechoic center if hemorrhage
  • Well demarcated with peripheral enhancement
  • Homogenous more often than heterogeneous
  • Hypodense if steatotic
  • Hyperdense if hemorrhagic
  • HNF1 α: signal lost on chemical shift; moderate arterial enhancement without persistent enhancement during delayed phase
  • IHCA: markedly hyperintense on T2 with stronger signal peripherally; persistent enhancement in delayed phase
  • β-Catenin: inflammatory subtype has same appearance as IHCA
    • Noninflammatory is heterogeneous with no signal dropout on chemical shift
    • Isointense of T1 and T2 with strong arterial enhancement and delayed washout
Hemangioma
  • Hyperechoic with well-defined rim and with few intranodular vessels
  • Discontinuous peripheral nodular enhancement
  • Isoattenuating to aorta with progressive centripetal fill-in
  • T1: hypointense; discontinuous peripheral enhancement with centripetal fill-in
  • T2: hyperintense relative to spleen
FNH
  • Generally isoechoic
  • Central scar
  • Arterial phase shows homogenous hyperdense lesion
  • Returns to precontrast density during portal phase that is hypo or isodense
  • T1: isointense or slightly hypointense. Gadolinium produces early enhancement with central scar enhancement during delayed phase
  • T2: slightly hyperintense or isointense
NRH Isoechoic/hyperechoic
  • Nonenhancing nodules, sometimes hypodense, with variable sizes (most sub-centimeter)
  • T1: hyperintense
  • T2: varied intensity (hypo/iso/hyperintense)

References

  1. Bonder A, Afdhal N (2012). "Evaluation of liver lesions". Clin Liver Dis. 16 (2): 271–83. doi:10.1016/j.cld.2012.03.001. PMID 22541698.

Template:WH Template:WS