| |
The hepatitis
C virus (HCV), which was first detected in 1989, is spread by direct
contact with infected blood of body fluids. It affects approximately
two per cent of the population. Risk factors include intravenous
drug use, intranasal cocaine use, tattoos and body piercing with
non-sterile equipment, blood transfusions (especially prior to 1990),
long-term hemodialysis and organ transplantation.
The risk of
acquiring the infection after transfusion from an anti-HCV antibody-positive
donor is greater than 80 per cent. HCV infection is frequently asymptomatic
and liver enzymes may be normal. Approximately 70 per cent develop
chronic hepatitis. This is a significant infection since cirrhosis
develops in one-half to one-third of people with chronic hepatitis,
and hepatocellular carcinoma in four per cent. The risk of cirrhosis
is increased with excessive alcohol consumption and concurrent hepatitis
B infection. There are different strains or genotypes of this RNA
virus. Some genotypes, such as 1b, are associated with chronicity
and progression.
Many extrahepatic
diseases have been associated with HCV infection. Cutaneous manifestations
are common and may be the first suggestion of infection. They are
discussed on pages 1 and 23. Pruritus and xerostomia are common,
although xerophthalmia and anti-Ro antibodies are not features.
Cry globulin-associated vasculitis is present in about one-quarter
of patients. Conversely, approximately 80 per cent of mixed cryoglobulinemia
is related to hepatitis C infection. Clinical manifestations include
palpable purpura, arthralgias and weakness; other organs such as
the brain and kidney can also be affected. Antiviral therapy usually
results in clinical improvement. Porphyria cutanea tarda is associated
with HCV in 10 to 90 per cent of cases. Some studies have also shown
an association with lichen planus and polyarteritis nodosa.
In conclusion,
skin disease may be the initial presentation of HCV infection. Patients
with mixed cryoglobulinemia, porphyria cutanea tarda, and those
at higher risk for HCV who have any of the other disorders discussed
above, should be tested for anti-HCV antibodies. Liver function
testing is not sufficient since liver enzymes may be normal.
|
|