Multiple endocrine neoplasia type 1 differential diagnosis

Multiple endocrine neoplasia type 1 Microchapters
Home
Patient Information
Overview
Historical Perspective
Classification
Pathophysiology
Causes
Differentiating Multiple endocrine neoplasia type 1 from other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications and Prognosis
Diagnosis
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
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
Multiple endocrine neoplasia type 1 differential diagnosis On the Web
Most recent articles
Most cited articles
Review articles
CME Programs
Powerpoint slides
Images
American Roentgen Ray Society Images of Multiple endocrine neoplasia type 1 differential diagnosis All Images X-rays Echo & Ultrasound CT Images MRI
Ongoing Trials at Clinical Trials.gov
US National Guidelines Clearinghouse
NICE Guidance
FDA on Multiple endocrine neoplasia type 1 differential diagnosis
CDC on Multiple endocrine neoplasia type 1 differential diagnosis
Multiple endocrine neoplasia type 1 differential diagnosis in the news
Blogs on Multiple endocrine neoplasia type 1 differential diagnosis
Directions to Hospitals Treating Multiple endocrine neoplasia type 1
Risk calculators and risk factors for Multiple endocrine neoplasia type 1 differential diagnosis

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

Overview

Multiple endocrine neoplasia type 1 must be differentiated from other diseases that cause hyperparathyroiodism, gastric ulcers, and neurological symptoms such as von Hippel-Lindau syndrome, tuberous sclerosis, carney complex, neurofibromatosis type 1, Li-Fraumeni syndrome, multiple endocrine neoplasia type 2, familial hyperparathyroidism, pheochromocytoma and acromegaly.

Differential Diagnosis

• von Hippel-Lindau syndrome
• Tuberous sclerosis
• Carney complex
• Neurofibromatosis type 1
• Li-Fraumeni syndrome
• Inherited pancreatic endocrine tumor syndromes
• Familial adenomatous polyposis/Gardner syndrome
• Multiple endocrine neoplasia type 2
• Cowden syndrome
• Familial Cushing's syndrome
• Multiple endocrine neoplasia type 4
• Isolated familial acromegaly/gigantism
• Familial primary aldosteronoma
• Familial isolated pituitary adenoma
• Familial isolated hyperparathyroidism
• Familial papillary thyroid carcinoma
• Familial isolated pheochromocytoma/paraganglioma
• Inherited adrenocortical carcinoma