Amyloidosis MRI: Difference between revisions

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===Images===
===Images===
[[File:Cardiac-amyloidosis-3.jpg|300px|left|thumb| MRI showing cardiac amyloidosis (yellow arrow). <ref>Case courtesy of Dr David Cuevas, <a href="https://radiopaedia.org/">Radiopaedia.org</a>. From the case <a href="https://radiopaedia.org/cases/61600">rID: 61600</a></ref>]]
[[File:Cardiac-amyloidosis-3.jpg|300px|left|thumb| MRI showing cardiac amyloidosis (yellow arrow). <ref>Case courtesy of Dr David Cuevas, <a href="https://radiopaedia.org/">Radiopaedia.org</a>. From the case <a href="https://radiopaedia.org/cases/61600">rID: 61600</a></ref>]]
[[File:Hypothalamic-amyloidoma-1.jpg|300px|center|thumb| MRI showing hypothalamic amyloidosis (yellow arrows). <ref>Case courtesy of Dr Rebecca Dumont Walter, <a href="https://radiopaedia.org/">Radiopaedia.org</a>. From the case <a href="https://radiopaedia.org/cases/42915">rID: 42915</a></ref>]]
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== References ==
== References ==
{{reflist|2}}
{{reflist|2}}

Latest revision as of 01:41, 26 October 2019

Amyloidosis Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Primary amyloidosis
Secondary amyloidosis
Familial amyloidosis
Wild-type (senile) amyloidosis
Cardiac amyloidosis
Beta-2 microglobulin related amyloidosis
Gelsolin related amyloidosis
Lysozyme amyloid related amyloidosis
Leucocyte cell-derived chemotaxin 2 related amyloidosis
Fibrinogen A alpha-chain associated amyloidosis

Pathophysiology

Causes

Differentiating Amyloidosis from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

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MRI

Other Imaging Findings

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Risk calculators and risk factors for Amyloidosis MRI

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

Overview

MRI is commonly done to assess for amyloid deposition in particular organs. It can also be done to rule out other causes of organ dysfunction. However, MRI is more sensitive than CT in the diagnosis of amyloidosis. A cardiac MRI is used when an echocardiogram fails to differentiate amyloidosis from hypertrophic cardiomyopathy.

MRI

In cardiac amyloidosis the MRI findings may include[1]:

  • Heart enlargement with heterogeneous decreased attenuation
  • Cardiac calcifications
  • Pericardial effusion (rare)

In hepatic amyloidosis the MRI scan findings may include:

  • Liver enlargement with heterogeneous decreased attenuation
  • Asymmetric and triangular hepatomegaly with the apex at the falciform ligament (due to mild atrophic change of the lateral border of both hepatic lobes)
  • Parenchyma calcification (rare)

In renal amyloidosis the MRI findings may include:

  • Kidney enlargement with heterogeneous decreased attenuation
  • Parenchyma calcification (rare)

In amyloidosis involving the peripheral nerves the MRI findings may include:

  • Perineural enhancement

Images

MRI showing cardiac amyloidosis (yellow arrow). [2]
MRI showing hypothalamic amyloidosis (yellow arrows). [3]


References

  1. Falk RH, Quarta CC, Dorbala S (2014). "How to image cardiac amyloidosis". Circ Cardiovasc Imaging. 7 (3): 552–62. doi:10.1161/CIRCIMAGING.113.001396. PMC 4118308. PMID 24847009.
  2. Case courtesy of Dr David Cuevas, <a href="https://radiopaedia.org/">Radiopaedia.org</a>. From the case <a href="https://radiopaedia.org/cases/61600">rID: 61600</a>
  3. Case courtesy of Dr Rebecca Dumont Walter, <a href="https://radiopaedia.org/">Radiopaedia.org</a>. From the case <a href="https://radiopaedia.org/cases/42915">rID: 42915</a>

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