DOI:10.2214/AJR.04.1363
AJR 2006; 187:90-98
© American Roentgen Ray Society
Transvaginal Sonography as an Adjunct to Endorectal Sonography in the Staging of Rectal Cancer in Women
Kavita P. Dhamanaskar1,2,
Wendy Thurston3 and
Stephanie R. Wilson1
1 Department of Medical Imaging, Toronto General Hospital, University of
Toronto, 585 University Ave., Toronto, ON M5G 2C4, Canada.
2 Present address: Diagnostic Imaging, Henderson General Hospital, Hamilton, ON
L8V 1C3, Canada.
3 Department of Medical Imaging, St. Joseph's Health Centre, University of
Toronto, Toronto, ON M6R 1B5, Canada.
Received August 30, 2004;
accepted after revision April 19, 2005.
Address correspondence to S. R. Wilson
(stephanie.wilson{at}uhn.on.ca).
Abstract
OBJECTIVE. The purpose of this study was to evaluate the
contribution of transvaginal sonography (TVS) in the staging of rectal cancer
in women.
MATERIALS AND METHODS. Sixty women with rectal tumors underwent TVS.
Forty-five of the 60 women also underwent endorectal sonography. Forty-nine of
the women had rectal carcinoma; nine, tubulovillous adenoma; and two,
gastrointestinal stromal tumor confirmed at surgical pathologic examination
(n = 41) and biopsy before chemoradiation therapy (n = 19).
Four of the 49 rectal carcinomas were T1; seven, T2; 35, T3; and three, T4.
Images from TVS and endorectal sonography were shown independently to two
blinded reviewers, who staged the tumors and assessed examination adequacy for
tumor presence, size, and depth and nodal status. Staging results with TVS
were compared with those obtained with endorectal sonography and
histopathologic examination.
RESULTS. All tumors were seen with TVS. In 30 of the 49 rectal
carcinomas confirmed at surgical pathologic examination TVS tumor staging was
accurate in 25 (83.3%) of the cases. Two (6.7%) of the 30 tumors were
understaged, and 3 (10%) were overstaged. All tumors selected for
chemoradiation (n = 19) were correctly staged T3. Endorectal
sonography was suboptimal for tumors that were stenotic (n = 3),
large (n = 2), high at the rectosigmoid junction (n = 4), or
low at the anal canal (n = 3). In these 12 cases, TVS successfully
depicted the lesion, and the images gave enough information for prediction of
stage. In interpretation of the images of 45 patients who underwent both TVS
and endorectal sonography, the blinded reviewers had good agreement and
comparable accuracy for staging in adequate examinations with each technique.
Four of the nine villous adenomas were overstaged as T1 on TVS.
Gastrointestinal stromal tumors manifested as intramural vascular masses.
CONCLUSION. TVS is an excellent adjunct to endorectal sonography in
the staging of rectal cancer in women. It helps resolve the findings after
endorectal sonography has been unsuccessful because the tumors are stenotic or
in a high or low position.
Keywords: cancer colon gastrointestinal radiology oncologic imaging rectum sonography
Introduction
Endorectal sonography is preferred to CT and conventional MRI in the
preoperative local staging of rectal tumors
[1-5].
The capability of sonography to resolve the layers of the rectal wall
facilitates assessment of depth of invasion and thereby of precise tumor stage
[6,
7]. Accurate tumor staging
affects patient care because adjuvant therapy has an important role in the
management of stage T3 and T4 disease, whereas local excision is preferred for
T1 tumors
[8-10].
Studies comparing CT with endorectal sonography have shown superior results
with endorectal sonography for the assessment of both depth of invasion and
lymph node involvement [2,
3]. The accuracy of endoluminal
sonography is 69-97%, whereas that of CT is 41-82%
[1-5,
11-15].
An important role of CT, however, is assessment of distant metastasis and
contiguous organ involvement in advanced cancers
[5,
16]. Therefore in many centers
the combination of endorectal sonography and abdominal and pelvic CT is an
accepted pretreatment strategy in the care of patients with rectal cancer.
Conventional MRI has proven to be inferior to endorectal sonography in the
definition of the layers of the rectal wall. The accuracy rate is similar to
that of CT
[17-19].
However, the superior spatial resolution and anatomic detail afforded by
endorectal surface coils have allowed equivalent efficacy, ranging from 70% to
90% in a number of small studies, to sonography in local staging of rectal
tumors
[20-22].
In the assessment of regional lymph nodes, endorectal MRI has not proven to be
superior to endorectal sonography
[23,
24]. Comparisons of endorectal
sonography with double-contrast MRI have shown similar accuracy rates
[25-27].

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Fig. 1A Advantages of sodium phosphate (Fleet Phospho-Soda, CB Fleet)
enema. Transverse transvaginal sonographic (TVS) image of normal rectum in
62-year-old woman. Fluid (F) in rectal lumen appears black. Rectum is evident
in its entirety as multilayered ring. All five layers of rectal wall are well
delineated.
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Fig. 1B Advantages of sodium phosphate (Fleet Phospho-Soda, CB Fleet)
enema. Transverse TVS image of rectum in 67-year-old woman shows large
polypoid rectal mass (M) outlined by enema solution (arrows).
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Although endorectal sonography for many years has been the chosen method
for assessing rectal tumors, the technique has limitations. The disadvantages
include limited ability or failure to depict stenotic tumors and anal
strictures and lack of or poor visualization of high rectal tumors and those
situated low in the rectum, just above or involving the anal canal
[28]. Perhaps most important,
however, are limitations of equipment and probe design. Rotating transducer
crystals for axial imaging traditionally available for endorectal sonography
have image quality and resolution inferior to those afforded by end-fired
transvaginal probes operating on state-of-the-art high-end sonographic
equipment. Because the resolution of a transducer is related to its aperture
size or footprint, the effective aperture of a curved array transducer, such
as that used in most transvaginal probes, is greater than that of a
mechanically steered transducer and allows superior image resolution
[29].
Transvaginal sonography (TVS) performed with a high-frequency end-fired
probe placed in the vagina provides excellent-resolution images of not only
the uterus and ovaries but also of the portions of the urinary and
gastrointestinal tracts close to the vaginal vault. TVS has been used with
variable success in the assessment of nongynecologic pathologic conditions
within reach of a vaginal probe
[30,
31]. The fixed position of the
rectum deep in the pelvis directly posterior to the vagina is a prime choice
for study by the transvaginal approach. Our objective was to assess the role
of TVS in the staging of rectal cancer in women, especially in instances in
which examination was difficult or considered a failure with traditional
endorectal sonography.
Materials and Methods
Patient Population
A retrospective study was conducted with the records of 60 women (age
range, 35-81 years) in two medical centers who underwent endoluminal
sonography for staging of rectal tumors between January 2000 and December
2003. Forty-five of the 60 patients underwent endorectal sonography that was
followed by TVS at the larger center. Fifteen patients underwent TVS alone at
the other institution. Selection of patients for both studies or one study was
related only to the center at which sonography was performed. Patients who
underwent only endorectal sonography in the time frame of the study were not
included in the study. We received ethics committee approval for chart
review.
Final pathologic results on the 60 tumors included 49 rectal carcinomas,
nine tubulovillous adenomas, and two cases of gastrointestinal stromal tumor
(GIST). Tumor size ranged from 1.0 to 8.0 cm. Surgical pathologic confirmation
was obtained for 30 of the 49 rectal carcinomas, all nine tubulovillous
adenomas, and both cases of GIST. Nineteen cases of locally invasive rectal
carcinoma were confirmed by biopsy before chemoradiation therapy. The final
tumor stage for the 49 rectal carcinomas was based on comprehensive clinical,
colonoscopic, radiologic, and pathologic correlation. Four of the 49 rectal
carcinomas were stage T1; seven, T2; 35, T3; and three, T4. Surgical
confirmation of locoregional metastatic lymphadenopathy was obtained in 10
cases.
Imaging Techniques
At the larger institution involved in this study, a physician experienced
in endorectal sonography and TVS obtained all the scans. Both examinations
were performed on the same day, and a single comprehensive report of tumor
stage was generated. The technical feasibility and effectiveness of TVS in
comparison with endorectal sonography were documented at the time of the
procedure. At the secondary institution, 15 cases of rectal carcinoma were
staged only with TVS by a physician initially trained at the larger
institution.
All patients received a sodium phosphate (Fleet Phospho-Soda, CB Fleet)
enema 1 hour before the examination (Figs.
1A and
1B). A digital rectal
examination was performed immediately before TVS. TVS was performed with an
HDI 5000 scanner (Philips Medical Systems) with conventional end-firing 9- to
5-MHz TVS probes (C9-5, Philips) with the patient in the supine position.
Color Doppler assessment was performed for all the tumors imaged with TVS.
Endorectal sonography was performed with rotating axial 10-MHz and side-firing
biplane 7-MHz probes (type 8537, Bruel and Kjaer). The probe head used for
endorectal sonography was covered with a condom filled with 50 mL of degassed
water. A sonolucent plastic cone (type WA 0453, Bruel and Kjaer) was used if
evaluation of the anal canal was included in the tumor staging. All endorectal
sonographic examinations were performed before TVS.
Analysis
Blind interpretationA neutral person who was neither an
investigator nor a reviewer selected separate TVS and endorectal sonographic
image files for the 45 patients who underwent both procedures and for the 15
patients who underwent only TVS. Image files were shown independently to two
blinded reviewers, both of whom were investigators in the study but had not
seen any of the images in at least 6 months. The TVS and the endorectal
sonography images were incorporated into a file and randomized so that the TVS
image for a given patient was not shown to the reviewers in association with
its corresponding endorectal sonography scan. The reviewers assessed each
image file as either adequate or inadequate to determine tumor presence, size,
and depth of penetration and nodal status. Then they determined a sonographic
stage using the TNM criteria (Table
1) [32]. In case
of disagreement between reviewers for a single technique, a consensus stage
was obtained at a separate meeting.
Technical comparison: endorectal sonography versus
TVSImages from endorectal sonography and TVS for each patient were
studied side by side to determine the image quality of a technique as
equivalent, superior, or inferior to that of the other.
Correlation of TVS staging with histopathologic findingsIn
the 30 cases in which surgical pathologic correlation was available, the
consensus sonographic stage from the blind interpretation of TVS images was
compared with the histopathologic stage to establish the accuracy of TVS for
comparison with published results in the staging of rectal cancer by
endorectal sonography and other techniques.
Results
Blind Interpretation
Assessment in the blind interpretation for adequacy of examination showed
that TVS was successful in all 60 cases and that endorectal sonography was
successful in 37 of 45 cases in which that technique also was used. Assessment
of adequacy on both examinations included visualization of wall layers as
depicted in Figure 2. The blind
interpretation showed good agreement between the two reviewers with regard to
adequacy of examination and tumor staging with endorectal sonography and TVS.
The kappa coefficient was 0.85, indicating significant interreviewer agreement
(p < 0.001). In three cases in which the reviewers gave different
results of staging with a single technique, a consensus stage was reached at a
separate meeting after the blind interpretation.

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Fig. 2 Schematic shows gut signature. Cross-sectional
(left) and longitudinal (right) representations of
histologic layers of gut wall that correspond to the five layers seen on a
sonogram. Blue layers are hypoechoic, yellow and pink layers are
hyperechoic.
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Among the 45 patients who underwent endorectal sonography, there were eight
failed examinations, in which imaging was not possible, and four suboptimal
scans, in which the part of the tumor visible on the scan was staged.
Endorectal sonography was technically suboptimal in assessment of stenotic
tumors (n =3), large tumors (n = 2), tumors high at the
rectosigmoid junction (n = 4), and tumors low involving the anal
canal (n = 3). In the 37 cases in which images with both techniques
were available, the blind interpretation of tumor stage showed good agreement
between the techniques (
=0.78; p < 0.001)
(Table 2). In five (11%) of the
45 cases, staging was discordant between endorectal sonography and TVS, but
the tumor stage classifications differed by only one level.
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TABLE 2: Tumor Stage Comparison of Transvaginal Sonography and Endorectal
Sonography (n = 45) on the Basis of Consensus Tumor Stage Between Two
Reviewers
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Technical Comparison of Endorectal Sonography Versus TVS
For all pathologic conditions, endorectal sonography and TVS were judged of
equivalent efficacy in determination of tumor size and depth of penetration
and nodal status in 30 (67%) of 45 patients. TVS was judged by the reviewers
to be adequate for tumor staging in all 45 patients. In three (6.6%) of the 45
cases, TVS scans were suboptimal. The lesions in these cases were small
posterior tumors, and gas and fluid in the rectal lumen interfered with
visualization. Nonetheless, all of these tumors were both measured and staged
with TVS. Endorectal sonography was suboptimal in 12 (27%) of the cases. Eight
of the 12 examinations were assessed as complete failures, in which the tumor
was not visualized. In four of the 12 examinations, tumor assessment was
incomplete because of an inability to determine the extent of the tumor, but
the part of the tumor seen was staged. In all 12 cases, TVS was successful in
depicting the lesion and its extent, and the stage was correctly
predicted.
Correlation of TVS Staging with Histopathologic Findings
TVS stage of the 49 rectal carcinomas determined by blind interpretation
consensus was compared with histopathologic stage in the cases of the 30
patients who underwent surgery (Table
3). TVS was accurate in staging 25 (83.3%) of 30 tumors (Figs.
2,
3A, and
3B). Two (6.7%) of the 30
tumors were understaged, one of these T3 instead of T4, a clinically
inconsequential event. The other tumor was staged T2 instead of T3. In the
latter case, surgical pathologic examination showed only focal invasion of the
perirectal fat, and post-operative chemoradiation therapy was considered
adequate management. Three (10%) of the 30 tumors were overstaged. Two were
staged T2 instead of T1 and one T3 instead of T2. The case diagnosed T3 and
found to be T2 at pathologic examination was considered for surgery because
the lesion was fairly mobile at colonoscopy and because the sonographic
finding of mild irregularity of the perirectal fat layer in focal areas
suggested early T3 disease. The two tumors staged T2 instead of T1 with TVS
were polypoid tumors successfully resected at colonoscopy.
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TABLE 3: Tumor Staging of Rectal Carcinoma (n = 30): Transvaginal
Sonographic Stage (uT) Versus Surgical Histopathologic Stage (pT)
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Fig. 3A 65-year-old woman with T2 N0 rectal carcinoma. Both scans
show submucosa is penetrated by tumor and tumor involvement of muscularis
propria. Arrows mark border of submucosa at margin of tumor. Endorectal
sonogram obtained with axial rotating probe shows eccentric mass (M) between
11:30- and 4-o'clock positions. Mass obliterates submucosa and bulges deep
border of wall but does not show extension into perirectal fat.
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Fig. 3B 65-year-old woman with T2 N0 rectal carcinoma. Both scans
show submucosa is penetrated by tumor and tumor involvement of muscularis
propria. Arrows mark border of submucosa at margin of tumor. Transvaginal
sonogram shows mass (M) of similar size and location to that in A.
Wall-layer definition is superior to and border of submucosa at margin of
tumor (arrows) is better delineated than in A. Disruption of
involved layers is evident.
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Sensitivity and specificity for staging of rectal cancer with TVS were
determined by comparison of sonographic stage with histopathologic results in
the 30 cases in which rectal carcinoma was surgically removed. Comparison of
tumor confined within the bowel wall (stages T1 and T2) and tumor that
extended beyond the bowel wall (stages T3 and T4) yielded a sensitivity of
94.7% and a specificity of 90.9% (Table
4).
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TABLE 4: Staging of Rectal Carcinoma (n = 30) Within Bowel Wall and
Tumor Extending Beyond Bowel Wall: Transvaginal Sonographic Stage Versus
Surgical Histopathologic Stage
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The 19 (39%) of 49 patients with biopsyproven rectal cancer who did not
undergo surgery had either advanced T3 or T4 disease and underwent neoadjuvant
chemoradiation therapy before consideration for surgery (Figs.
5A,
5B, and
5C). Because we did not have
gross anatomic pathologic results for these patients, their data were not
included in the calculation of sensitivity and specificity. In all 19 cases,
sonographic local staging showed clear T3 disease on the basis of destruction
of all wall layers by the tumor and extension into the perirectal fat. The
finding of T4 disease in two of the 19 patients was based on CT and MRI
findings.

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Fig. 5A 76-year-old woman with gross T3 rectal carcinoma seen on
transvaginal sonography (TVS) after failed endorectal sonography. Long-axis
(A) and transverse (B) TVS images show large hypoechoic
stenosing tumor with complete loss of wall-layer definition. Lumen (L) is
narrowed. Gross invasion of perirectal fat (arrows) is evident in
B.
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Fig. 5B 76-year-old woman with gross T3 rectal carcinoma seen on
transvaginal sonography (TVS) after failed endorectal sonography. Long-axis
(A) and transverse (B) TVS images show large hypoechoic
stenosing tumor with complete loss of wall-layer definition. Lumen (L) is
narrowed. Gross invasion of perirectal fat (arrows) is evident in
B.
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Fig. 5C 76-year-old woman with gross T3 rectal carcinoma seen on
transvaginal sonography (TVS) after failed endorectal sonography. Sagittal TVS
image through mesorectum shows three lymph nodes (arrows) in
perirectal fat. Patient underwent preoperative chemoradiation therapy.
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TVS staging of four of the nine tubulovillous adenomas was inaccurate
because the lesions were overstaged T1 instead of mucosal lesions (T0). Five
of the nine tumors were correctly staged (Figs.
6A,
6B, and
6C). Because the surgery for
both villous adenoma and T1 tumors is transanal excision, the overstaging did
not affect patient management. In this study population, three of five
tubulovillous adenomas overstaged T1 with endorectal sonography were correctly
predicted to be T0 with TVS (Table
2) and were confirmed at excision. The other four patients
underwent TVS but not endorectal sonography. The origin and pathologic
features of the two cases of GIST (Figs.
7A and
7B) were correctly predicted
with TVS.

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Fig. 6A 57-year-old woman with tubulovillous adenoma. Endorectal
sonogram obtained with rotating axial probe shows eccentric mass (m) in
anterior aspect between the 11-o'clock and 3-o'clock positions. Wall layering
is not well defined at base of tumor, but tumor does not extend into
perirectal fat. Polypoid intraluminal nature of mass is not evident because
inflated rectal balloon compresses soft tumor into rectal wall. Arrowheads
indicate submucosa.
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Fig. 6B 57-year-old woman with tubulovillous adenoma. Sagittal
transvaginal sonogram shows polypoid intraluminal mass (m) outlined by enema
fluid and clearly defined submucosa (arrowheads). Suggestion of wall
disruption (arrow) is evident at base of stalk.
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Fig. 6C 57-year-old woman with tubulovillous adenoma. Projection in
B with addition of color Doppler shows disruption is related to
vascular stalk of tumor rather than tumor invasion through rectal wall.
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Fig. 7A 46-year-old woman with asymptomatic gastrointestinal stromal
tumor. Sagittal transvaginal sonogram shows large hypoechoic mass (M) related
to anterior rectal wall and arising from outer hypoechoic layer, muscularis
propria. Submucosa is intact. Arrows outline two echogenic layers that
constitute submucosa of anterior and posterior rectal wall. Luminal surfaces
are in apposition and appear as gray line between two echogenic layers.
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Lymph nodes in the perirectal fat and mesorectum (Figs.
8A and
8B) were detected with TVS in
22 of 49 patients with rectal carcinoma. Lymph node size ranged from 3 to 20
mm on sonography, and all nodes were reported regardless of size. Surgical
confirmation of node-positive disease was obtained in 10 of these 22 patients.
The other 12 patients in whom nodes were depicted with TVS had gross T3
disease and were treated with chemoradiation therapy before surgery. Therefore
the histologic features of the nodes were not confirmed. In 4 of the 22
patients, TVS depicted nodes in the mesorectum well removed from the tumor
that were not visualized on endorectal sonography. In this small study
population, we did not find lymph nodes on sonography that had negative
results at pathologic examination.

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Fig. 8A 35-year-old woman with invasive rectal cancer and necrotic
lymphadenopathy. Transverse transvaginal sonogram of rectovaginal septum shows
two large nodes (arrows) with necrotic centers.
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Fig. 8B 35-year-old woman with invasive rectal cancer and necrotic
lymphadenopathy. Axial CT scan shows two large nodes (long arrows)
depicted in A and diffuse rectal wall thickening (short
arrows) not shown in A.
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Fig. 4A 70-year-old woman with T3 N0 rectal carcinoma confirmed at
surgery. Axial endorectal sonogram shows penetration of all rectal wall layers
with irregularity of deep border of mass (M) into perirectal fat
(arrows).
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Fig. 4B 70-year-old woman with T3 N0 rectal carcinoma confirmed at
surgery. Transverse transvaginal sonogram shows concordant information with
convincing evidence of irregular extension of tumor (M) into perirectal fat
(arrows).
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Discussion
Because of its proven efficacy in resolution of the layers of the rectal
wall, sonography continues to be the best imaging technique for local staging
of rectal tumors
[1-11].
Our initial experience with TVS for staging of rectal cancer was with patients
with rectal tumors who underwent inadequate endorectal sonography (n
= 12). TVS frequently resolves the limitations posed by endorectal sonography
in women with rectal cancer. In patients with stenotic tumors, the endorectal
probe may not be advanced into the rectum beyond the tumor and therefore is
limited in defining tumor extent. The TVS approach clearly defines the
superior and inferior tumor extent and helps determine the depth of invasion
(Figs. 9A and
9B). In the four patients with
tumors high in the rectum close to the rectosigmoid junction, the tumors were
visualized only on TVS. Endorectal sonography did not show the tumor because
of the limitations of probe length and the fixed direction of insonation of a
side-fired probe (Figs. 10A
and 10B). Use of an end-fired
transvaginal probe allowed a much more flexible and greater field of view.
Anal canal involvement was easily assessed with TVS in all patients, and TVS
caused less discomfort than did endorectal sonography (Figs.
11A,
11B, and
11C). Furthermore, TVS can be
performed with conventional probes used for routine pelvic examinations.

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Fig. 9A 56-year-old woman with large stenotic rectal tumor.
Endorectal sonographic examination failed. Transverse (A) and sagittal
(B) transvaginal sonograms show extensive circumferential rectal wall
tumor (T), destruction of wall layers, irregular residual lumen
(arrows, A), and perirectal lymphadenopathy (arrows,
B). Images show tumor only with no normal bowel wall. Lumen is
obliterated and visible as central irregular white line related to residual
luminal content, air, or both.
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Fig. 9B 56-year-old woman with large stenotic rectal tumor.
Endorectal sonographic examination failed. Transverse (A) and sagittal
(B) transvaginal sonograms show extensive circumferential rectal wall
tumor (T), destruction of wall layers, irregular residual lumen
(arrows, A), and perirectal lymphadenopathy (arrows,
B). Images show tumor only with no normal bowel wall. Lumen is
obliterated and visible as central irregular white line related to residual
luminal content, air, or both.
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Fig. 10A 51-year-old woman with T2 cancer of rectosigmoid junction not
seen on endorectal sonography. Transvaginal images show eccentric hypoechoic
mass (m) in bowel. Destruction of echogenic wall layer represents submucosa
with infiltration through hypoechoic muscularis propria. Perirectal fat is not
invaded. Transverse image.
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Fig. 10B 51-year-old woman with T2 cancer of rectosigmoid junction not
seen on endorectal sonography. Transvaginal images show eccentric hypoechoic
mass (m) in bowel. Destruction of echogenic wall layer represents submucosa
with infiltration through hypoechoic muscularis propria. Perirectal fat is not
invaded. Long-axis image shows rectal wall layers opposite tumor are
intact.
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Fig. 11A 62-year-old woman with cancer of anal canal. Transverse
(A) and long-axis (B) transvaginal sonograms show hypoechoic
mass (M) in anal canal close to anal verge. C, Color Doppler image
shows intense vascularity of mass.
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Definition of the rectal wall layers with TVS is comparable to that of
endorectal sonography. The layers are seen as five concentric rings consisting
of alternating hyperechoic and hypoechoic layers. The inner mucosa and outer
perirectal fat layer are bright, and the two hypoechoic layers contain the
muscle layers: muscularis mucosa and muscularis propria (Figs.
1A,
1B,
3A,
3B,
4A,
4B,
6A,
6B, and
6C). This arrangement allows
accurate assessment of depth of penetration. In our patient population that
had surgical pathologic correlation, TVS had 83.3% accuracy for correct
prediction of tumor stage with high sensitivity (95%) and specificity (91%)
for tumor invading through the bowel wall versus tumor limited to the bowel
wall (Table 4). These results
are comparable to the published data for endorectal sonography
[1-5].
Our findings are in agreement with published results of preliminary studies
that have shown the feasibility of TVS in staging rectal cancer with high
accuracy and technical competence
[33,
34]. Scialpi et al.
[35] described the use of a
water enema with TVS for local staging of advanced stenotic rectal tumors.
Fedyaev et al. [36] used TVS
with a waterfilled balloon in the rectal lumen for staging rectal cancer in
women. In our experience, Fleet enema was sufficient for both bowel
preparation and provision of the necessary amount of fluid to distend the
rectum. The luminal fluid served to enhance wall-layer definition and to
outline the intraluminal component of a polypoid mass (Figs.
1A and
1B). TVS was valuable for study
of all lesions regardless of size and stage. TVS was uniformly better at
delineating lymph nodes in the mesorectum because of the more compliant nature
of the vagina compared with the rectum and the enhanced field of view for
depth obtained with an end-fired probe.
TVS used alone has a limitation related to lack of a panoramic axial view
of the rectum such as that afforded by the rotating axial probe used with
endorectal sonography. Survey of the entire rectum therefore takes much longer
with TVS than with endorectal sonography. On endorectal sonography, the axial
scan performed with a rotating mechanical transducer crystal is excellent for
survey of the entire rectum and perirectal soft tissues. This capability is
most often beneficial when the tumor is not felt with digital rectal
examination before the procedure. Once it is localized with an axial probe,
the tumor can be studied in more detail with a biplane probe, which provides
better resolution than a mechanical rotating crystal.
The limitations of this study include its retrospective nature and the fact
that the same investigator performed both TVS and endorectal sonography at a
single visit. Nonetheless, the examinations were performed with separate
sonographic machines, making it possible to separate image files for each
technique on our PACS and facilitating retrieval and selection for blind
interpretation. Endorectal sonography was always performed before TVS, which
may have introduced a bias. However, the initial interpretation was not used
for the comparison of staging with histopathology. Furthermore, the person
performing the initial interpretation of the scans also participated in the
blind interpretation. We believe that this is not problematic because staging
a tumor on the basis of a sonogram is not highly subjective and reflects a
simple interpretation as to the degree of invasion of the rectal wall. In
addition, the number of patients was comparatively small, and our association
with a large oncology facility may have presented us with an unusually large
percentage of tumors at an advanced stage.
Perhaps the most important limitation of this study relates to the lack of
confirmatory surgical histopathologic results for the 19 patients with rectal
cancer who had advanced invasive T3 tumors on TVS, endorectal sonography, or
both and underwent chemoradiation therapy with biopsy before surgery was
considered. Before the start of this retrospective review, the standard of
practice at our institution had been to confirm clinically suspect T3 disease
by endorectal sonography and biopsy before administration of neoadjuvant
therapy. The treatment of the 19 patients with gross T3 disease therefore
complied with our institutional practices. Surgical pathologic results are
rarely available for this patient population. Our results showed excellent
agreement of endorectal sonographic and TVS findings in all stages of rectal
cancer (Table 2). Furthermore,
in the 17 patients with stage T3 disease for whom there was pathologic
correlation, TVS stage and pathologic stage were in complete agreement
(Table 3). We therefore believe
that inclusion of this group of patients is reasonable. All patients with T3
disease who received radiation therapy underwent clinical evaluation by an
experienced colorectal and oncology specialist. Having for many years
performed digital rectal examinations on all patients undergoing endorectal
sonography for staging of rectal tumors, we believe large, hard, fixed
invasive tumors are much different from other tumors at digital examination.
In fact, the requisitions that we receive on this group of patients usually
request confirmation of T3 disease whereas other requisitions request staging
of rectal tumors.
Another limitation of our study was that the investigators performed the
blind interpretation of image files organized by a neutral third person. This
procedure was necessary because we lacked staff trained in and capable of
interpreting images obtained with endorectal sonography and TVS. We believe
our method was reasonable because a minimum of 6 months, and in most instances
more than 6 months, had passed between sonographic examination and blind
interpretation. In addition, the reviewers were not providing a diagnosis;
they were staging the tumors and assessing the adequacy of examinations.
We learned a great deal about tubulovillous adenoma since the beginning of
the retrospective review. A TVS approach allowed us for the first time to see
the soft, pliable nature of these tumors, which are often very large.
Real-time evaluation with compression of the tumors with the vaginal probe
allowed us to better visualize the intraluminal portion of the tumors and
their hypervascular stalks and showed continuous submucosa at the level of the
tumor stalk. Use of TVS allowed us to avoid our previous tendency toward
overstaging these superficial tumors as T1 rather than T0 because of
compression of the soft tumor into the adjacent rectal wall with the axial
endorectal ultrasound probe covered by an inflated balloon (Figs.
5A,
5B, and
5C). Although using both TVS
and endorectal sonography we overstaged some tubulovillous adenomas in this
study, we overstaged three of five tumors with endorectal sonography but
correctly staged them with TVS (Table
2) as confirmed at pathologic examination of the excised lesion.
Differentiation of T0 and T1 disease remains a difficult task with any
sonographic examination.
No questionnaire either oral or written was given to our patients regarding
their preference of procedure. Nonetheless, at our institution and others, TVS
is routinely used for gynecologic examinations and is not considered invasive,
painful, or otherwise troublesome. In all of the cases of rectal cancer in our
study, there were no technical problems or instances of patient
dissatisfaction with TVS. Endorectal sonography, however, is often associated
with considerable patient anxiety and, in some patients, rectal and anal
discomfort. We have found that rectal discomfort is much more frequently
encountered in patients with large rectal tumors than in patients undergoing
endorectal sonography for other indications, such as prostate evaluation.
In conclusion, our study showed successful TVS evaluation of all rectal
tumors in which it was attempted, including stenotic tumors and those
involving both the anal canal and the rectosigmoid region. These sites are
well recognized as potential problem areas for endorectal sonography. We
consider TVS an excellent adjunct to endorectal sonography for staging rectal
cancer, and we believe that particular benefit is appreciated in difficult
cases.
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