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Ulcerative colitis: patterns of involvement in colorectal biopsies
and changes with time.Am
J Surg Pathol. 1998 Aug;22(8):983-9.
Chronic
inflammation, both endoscopic and histologic, in a contiguous and
symmetric distribution is said to be important in distinguishing
ulcerative colitis (UC) from Crohn's disease. Little is known
whether this rule holds during the course of the disease and whether
endoscopic/histologic correlation persists. In this study, we
analyzed histologic patterns of UC in sequential sets of biopsy
specimens to assess whether endoscopic and histologic findings
correlate with time and treatment and to see whether distribution
changes. Two hundred seventeen sets of colorectal biopsy specimens
from 797 sites from 41 patients with clinical UC were studied and
correlated with endoscopic findings. Each biopsy specimen was
classified as definite or suspicious for chronic colitis or normal.
Two histologic patterns of disease were identified: (1) diffuse,
when all areas in all pieces from a biopsy segment had clear-cut
colitis and (2) nondiffuse, when not all pieces were involved or
single pieces had disease and normal mucosa both. Of 41 patients,
the maximal extent of histologic disease was pancolitis in 30; 25
had less extensive disease at some point in the course. The maximal
extent was left-sided in eight patients, seven of whom had less
extent at some point. Of the three patients in whom the maximal
extent was proctosigmoiditis, in one the inflammation disappeared.
Seventy percent of the biopsy sites had diffuse patterns and 30% had
nondiffuse. Histologic and endoscopic disease reverted to normal in
22 and 24 of 41 patients, respectively. Endoscopic and histologic
findings were similar in 65% of the biopsy sites. Our results
indicate that in long-standing UC (1) histologic disease may revert
to normal mucosa, (2) because endoscopy alone may be insufficient to
identify the mucosa as normal, biopsies should also be performed on
the endoscopically normal mucosa, (3) the full extent of UC often is
not established by a single set of biopsies, and (4) nondiffuse
chronic inflammation and rectal sparing occurs in UC and are not
necessarily markers of Crohn's disease.
Endoscopic and histological patchiness in treated ulcerative
colitis.
Am J Gastroenterol. 1999 Nov;94(11):3258-62.
OBJECTIVE: Traditionally, contiguous distribution of inflammation (endoscopic
and histological) with rectal involvement is thought to be important in
distinguishing ulcerative colitis (UC) from Crohn's disease of the colon.
Little long-term data are available that prove whether this rule holds
during the course of disease as it is modified by time and treatment. The
aim of this study was to investigate the prevalence of endoscopic and
histological patchiness and rectal sparing in treated UC over time and to
correlate these findings with treatment at the time of endoscopy. METHODS:
Patients with well-established UC who underwent sequential colonoscopy or
flexible sigmoidoscopy with biopsies were included in this study.
Patients' medical records including endoscopy/biopsy reports and clinical
status/symptoms/treatment at the time of endoscopy were reviewed
retrospectively. RESULTS: A total of 32 patients (14 men, 18 women; median
age, 45 yr; median UC duration, 15 yr) underwent 175 sequential
endoscopies with biopsies (161 colonoscopies, 14 sigmoidoscopies; median,
five endoscopies per patient; range, 3-10). Endoscopic and/or histological
patchiness was present in 20 of 175 (11%) sequential endoscopies with
biopsies over time from 12 of 32 (38%) patients. Endoscopic and/or
histological rectal sparing was present in 27 of 175 (15%) of sequential
endoscopies with biopsies over time from 14 of 32 (44%) patients. Seven
patients had both patchiness and rectal sparing. Therefore, in 47 (27%)
follow-up endoscopies in 19 (59%) patients, there was either patchy
disease, rectal sparing, or both sometime during the course of disease
with treatment. There was no significant difference in treatment,
including steroid use and rectal therapy, between those with patchiness
and/or rectal sparing and those without. CONCLUSIONS: Contrary to
traditional teaching, endoscopic and histological patchiness of
inflammation and rectal sparing are common during the course of disease in
treated UC and seem to be unrelated to specific therapy.
Atypical rectosigmoid histology in children with newly diagnosed
ulcerative colitis.Am
J Gastroenterol. 1993 Dec;88(12):2034-7.
BACKGROUND: In the untreated patient with inflammatory colitis, rectal
sparing or patchy rectal inflammation is generally considered a sign of
Crohn's disease (CD), rather than ulcerative colitis (UC). METHODS: The
initial endoscopic rectosigmoid mucosal biopsies obtained at disease onset
from 12 untreated children with UC who ultimately required surgery were
blindly reviewed (randomly mixed with another 62 specimens obtained from
children with CD or treated UC). Biopsies were classified as typical UC if
there was diffuse, active inflammation and severe crypt destruction or
distortion. Those with patchy, active inflammation and only mild crypt
changes were classified as CD. Because all 12 subjects had ultimately been
proven to have UC by examination of a subtotal colectomy specimen, for the
purposes of this report biopsies read as either normal or CD were both
considered evidence of atypical UC with rectal sparing. RESULTS: Five of
12 subjects (seven biopsies) had atypical histology. Mild, patchy
inflammation was seen in six rectal or sigmoid biopsies, whereas one
rectal biopsy was normal. The remaining seven subjects (10 biopsies) had
diffuse inflammation. Two of five subjects with atypical biopsies had an
endoscopically normal rectosigmoid, one had patchy inflammation, and the
remaining two had diffuse endoscopic changes. All seven subjects with
typical UC histology had diffuse endoscopic changes. Subjects with
atypical findings could not be differentiated by age, duration, or types
of symptoms at presentation, years of disease at colectomy, or indications
for colectomy. CONCLUSIONS: Patchy or absent inflammation of the rectum
and sigmoid can be present in untreated children with UC at disease onset.
Because such children may be mistakenly diagnosed as having CD, these data
must be considered when treatments or clinical research protocols are
designed to include children with colitis. |