Adrenolipoma: Difference between revisions

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{{SK}} Adrenal myelolipoma
{{SK}} Adrenal myelolipoma
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== Overview ==
== Overview ==

Revision as of 18:13, 19 September 2012

Adrenolipoma

Adrenolipoma Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Adrenolipoma from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

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

Adrenolipoma On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Adrenolipoma

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X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Adrenolipoma

CDC on Adrenolipoma

Adrenolipoma in the news

Blogs on Adrenolipoma

Directions to Hospitals Treating Adrenolipoma

Risk calculators and risk factors for Adrenolipoma

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Adrenal myelolipoma

Overview

Adrenolipomas are benign tumors histologically consisting of fat and bone marrow in varying proportions. These tumors are benign. In general they are hormonally inactive, small (<5 cm) and unilateral. Adrenolipomas are rare benign neoplasms.They are made up of mature adipose tissue and a variable amount of hematopoietic elements. Most lesions are small and asymptomatic. They are usually discovered incidentally at autopsy or on imaging studies performed for other reasons. Most tumors are unilateral but show no predilection to one particular side. Tumor size varies from several millimeters to more than 30 cm.

Pathophysiology

A myelolipoma may represent a site of extramedullary hematopoiesis. The most widely accepted theory is the existence of metaplasia of the reticuloendothelial cells of blood capillaries in the adrenal gland in response to stimuli such as necrosis, infection, or stress.

Differential Diagnosis

That of an incidentaloma.

Epidemiology and Demographics

The incidence varies from 0.08-0.4% at autopsy.

Natural History

Benign. Adrenal hemorrhage is rare.

Diagnosis

CT

Patient #1: CT images demonstrate a large left myelolipoma

Patient #2: CT images demonstrate a left myelolipoma with a small amount of marcoscopic fat

Acknowledgements

The content on this page was first contributed by: C. Michael Gibson, M.S., M.D.




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