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Crohn’s disease (CD) and ulcerative colitis (UC) are the most common forms
of IBD. Although UC and CD are typically differentiated on the basis of
clinical, radiographic, and endoscopic findings, distinguishing between
these conditions can be difficult in about 10% to 15% of patients,
especially when disease is confined to the colon. Because the treatment and
prognosis of UC and CD differ, accurate diagnosis is critical for
management.
Numerous studies have investigated the utility of 2 serologic markers,
perinuclear anti-neutrophil cytoplasmic antibody (pANCA) and
anti-Saccharomyces cerevisiae antibody (ASCA), in differentiating between UC
and CD. The pANCA associated with IBD differs from that found in the
vasculitides, having an “atypical” perinuclear staining pattern that can be
identified by differential staining patterns with ethanol–formalin fixation.
This atypical pANCA is found in about 50% to 80% of UC patients but only 10%
to 30% of those with CD. ASCA, on the other hand, is more common in CD (46%–70%) than in UC (6%–12%).3,4 The combination of these markers has high
specificity for UC (94%–97%; pANCA+/ASCA-) and CD (81%–98%; ASCA+/pANCA-).5
Serologic results can also assist in stratification of CD: pANCA-positive CD
is associated with a clinical phenotype similar to that of UC (UC-like CD),4
while positivity for ASCA IgG and IgA is associated with non-UC-like
disease.6 Several reports have noted the potential utility of serologic
testing, combined with other clinical and laboratory information, to
identify children with suspected IBD who may not require invasive
testing.2,7 Proteinase 3 antibody and myeloperoxidase antibody assays are
supportive tests recommended by an international consensus group.8 |