Xanthoma: Difference between revisions
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*[[Diabetes Mellitus]] | *[[Diabetes Mellitus]] | ||
*[[Glycogenosis type 1a]] aka [[von Gierke disease]] aka [[Glucose-6-phosphatase deficiency]] aka [[Glycogen storage disease type 1a]] | *[[Glycogenosis type 1a]] aka [[von Gierke disease]] aka [[Glucose-6-phosphatase deficiency]] aka [[Glycogen storage disease type 1a]] | ||
*[[Hand-Schüller-Christian disease]] | *[[Hand-Schüller-Christian disease]] | ||
*[[Hypercholesterolemia]] | *[[Hypercholesterolemia]] | ||
Revision as of 21:26, 13 September 2011
| Xanthoma | |
 | |
|---|---|
| Photograph of patient's hands showing multiple xanthoma tendinosum. Kumar et al. Cases Journal 2008 | |
| ICD-10 | E78.2 (ILDS E78.280), K13.4 |
| ICD-9 | 272.2 |
| DiseasesDB | 28524 |
| MeSH | D014973 |
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
A xanthoma (or xanthomata or xanthomatosis) (from Greek xanthos, ξανθος, "yellow") is a deposition of yellowish cholesterol-rich material in tendons and other body parts in various disease states:
- Tendon xanthomas (associated with familial hypercholesterolemia, cerebrotendineous xanthomatosis and phytosterolemia]
- Palmar xanthomas
- Eruptive xanthomas
- Tubo-eruptive xanthoma
- Xanthoma tuberosum
Differential Diagnosis of Underlying Causes of Xanthoma
In alphabetical order. [1] [2]
- Alagille syndrome
- Amyloidosis
- Biliary Cirrhosis
- Cholestanol storage disease
- Chronic bile duct disease
- Chronic pancreatitis
- Diabetes Mellitus
- Glycogenosis type 1a aka von Gierke disease aka Glucose-6-phosphatase deficiency aka Glycogen storage disease type 1a
- Hand-Schüller-Christian disease
- Hypercholesterolemia
- Hypertriglyceridemia
- Juvenile xanthogranuloma
- Myxedema
- Nephrotic Syndrome
- Urticaria pigmentosa