Familial Hyperlipidemias See Table 3 -15 | | | | Table 3-15 Types of Familial Hyperlipidemia | | Type | | Defect | | ↑ CAD Risk | | Serum | | Lipid Levels | | Clinical Findings | | Type I
{Familial LPL deficiency Familial hyperchylomicronemia} | | ↓ Lipoprotein lipase (LPL) or apoprotein CII defect | | No | | Creamy top layer | | ↑↑ TG (chylomicrons) | | Eruptive xanthomas, acute pancreatitis abdominal pain, lipemia retinalis | | Type IIa
{Familial hypercholesterolemia Familial defective apo B100} | | LDL receptor defect (mutation of LDLR or apo B) | | Yes | | Clear | | ↑↑ Cholesterol (LDL) | | Tendinous and tuberous xanthomas, xanthelasma | | Type IIb
{Familial combined hypercholesterolemia} | | LDL receptor defect | | Yes | | Clear or cloudy | | ↑ Cholesterol ↑ TG (LDL, VLDL) | | Tendinous and tuberous xanthomas, xanthelasma | | Type III
{Familial dysbetalipoproteinemia} | | Apoprotein E defect | | Yes | | Turbid | | ↑ Cholesterol ↑ TG (IDL, VLDL) | | Xanthoma striatum palmare, {pathognomonic}
tuberous xanthomas | | Type IV
{Familial hypertriglyceridemia} | | ↑ Production of VLDL | | ± | | Turbid | | ↑ TG (VLDL, IDL) | | | | Type V | | Apolipoprotein C-II defect | | ± | | Creamy top layer | | ↑↑ TG ↑ Cholesterol (VLDL, chylo) | | | | | | | | | | | | | | |
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| | | | Table 3-16 Types of Xanthomas (Figure 3.20A–C) | | Type of Xanthoma | | Description | | Tuberous xanthomas (seen in type II, III) | | Pink-yellow papulonodules on extensor pressure surfaces, especially knees/elbows; slow to regress after initiation of treatment; seen in hypercholesterolemic states | | Tendinous xanthomas (II, III) | | Smooth nodular lipid deposits of the Achilles tendon > extensor tendons of hands, knees or elbows; may also see in hepatic cholestasis secondary to primary biliary cirrhosis | | Plane xanthomas (II, III) | | Yellow slightly elevated plaques typically involving eyelids, trunk, neck, shoulder or axillae; may also be from biliary cirrhosis; if normolipemic, may be associated with monoclonal gammopathy (IgG)
{Intertriginous almost pathognomonic for homozygous familial hypercholesterolemia} | | Xanthoma striatum palmare (III) | | Type of plane xanthoma over palm with yelloworange infiltration of volar creases (palms and fingers), characteristic for type III | | Xanthelasma (II, III) | | Plane xanthoma of eyelid; yellow flat-topped papules or plaques around medial eyelids; only half of patients with hyperlipidemia | | Eruptive xanthomas (I, IV, V)
{Do not confuse with xanthoma disseminatum} | | Eruption of small yellow papules with erythematous base on back, buttocks, chest, and proximal extremities; seen in hypertriglyceridemic state (often >3,000 mg/dl); associated with diabetes, pancreatitis, chronic renal failure | | | | | |
| | | | | | | Xanthoma disseminatum: occurs in normolipemic patients; red-yellow papules with flexural predilection | | | | | | | |
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