Minimal-change colitis and microscopic colitis are clinicopathological
terms for diarrhoea with normal endoscopic or barium enema findings.
Some controversy about the exact definitions and terminology still exi
sts. Some forms of minimal-change colitis may overlap with ''self-limi
ted'' colitis (infectious colitis) or may be due to (surreptitious) us
e of laxatives or other drugs. In recent years it has become clear how
ever that some genuine forms of chronic colitis can be diagnosed only
by microscopic examination of multiple colonic biopsies while macrosco
py is negative and hence can be called ''microscopic colitis''. Collag
enous colitis and lymphocytic colitis are at present two forms of this
type of colitis which are more or less well defined both clinically a
nd pathologically. Chronic watery diarrhoea is the main symptom for bo
th. The symptoms of collagenous colitis appear most commonly in the si
xth decade. Women are affected about 4 times more frequently than men.
The major microscopic characteristic is a thickened collagen layer un
derneath the intercryptal surface epithelium. The major characteristic
of lymphocytic colitis is an increase in number of interepithelial ly
mphocytes. Both conditions arc characterized by signs of mucosal infla
mmation. Clinically, collagenous colitis is characterized by long-last
ing diarrhoea. In patients with lymphocytic colitis the period of chro
nic diarrhoea is usually shorter and female predominance is less appar
ent. Although the natural history of these forms of colitis is not pre
cisely known, it appears from the data thus far published that the lon
g-term consequences are unlikely to be dire. The true incidence, aetio
logy and pathogenesis are unknown for both conditions and treatment is
unclear. Several studies of patients investigated for idiopathic chro
nic diarrhoea have shown that collagenous colitis and lymphocytic coli
tis are common disorders within these groups of patients (up to 27%).
It is important, therefore, to recognize the disease in order to reass
ure the patients and to avoid more expensive examinations. The diagnos
is can be made easily by obtaining multiple biopsies during colonoscop
y. One single rectal biopsy is indeed not enough as both lymphocytic a
nd collagenous colitis present as pancolitis and the microscopic diagn
ostic features may be variably expressed in different parts of the col
on.