A Shortfall of EUS in the Staging of Rectal Cancer Following Polypectomy

Theresa M. Smith, M.D.
John C. Deutsch, M.D.

 

Keywords

Rectal Cancer, Rectal Polyp, HNPCC, Rectal Ulcer

Introduction

A 50 year old man was referred for EUS evaluation of a rectal cancer following endoscopic polypectomy.

Methods for EUS Capture

EUS was done with a Pentax solid state radial solid probe at 6.5 mHz using water filled technique. Images were captured to SVHS tape and digitized using Adobe Premiere Software.

Case Summary

Figure 1

A 50-year-old male was referred for screening colonoscopy. His only complaint was rectal discharge that required him to return to the bathroom ten to fifteen minutes after a bowel movement. He denied any rectal bleeding or pain. The patient's past medical history was notable for a transitional cell carcinoma of the bladder which presented with gross hematuria at age 46. He had undergone cystoscopic resection and was being followed with cystoscopic exams every six months and had no evidence of recurrence. His family history was negative for colorectal cancer, uterine/ovarian cancer and genitourinary cancers.

Figure 2A

Figure 2B: Video clip of EUS showing tumor and additional hypoechoic area, probably representing an abnormal lymph node.

High Resolution Version
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His colonoscopy revealed the presence of a 2 cm polyp near the first valve of Houston, and smaller polyps at 70, 60, 45, 35 and 20 cm. The rectal polyp, as partially removed with a snare, and the pathology revealed a well to moderately differentiated adenocarcinoma arising in a tubulovillous adenoma (Figure 1). No lymphatic or vascular invasion was seen but the tumor extended in multiple fields to the cauterized polypectomy margins. The smaller polyps were all tubular adenomas.

Rectal EUS was performed two days after the rectal polypectomy. The EUS suggested this was a T2 lesion that measured 6 mm in thickness and 2.5 to 3.0 cm in width. There was no clear space between layer four and the tumor (Figure 2A,B). Just adjacent to the tumor there was a 5 mm hypodense area consistent with a small lymph node (Figure 2B). There was approximately 5 cm between the tumor and the anal verge. A representative corresponding visible human image is shown in Figure 3, and the approximate location of the tumor in the interactive visible human database is shown in Figure 4.

Figure 3

The rectal tumor was evaluated for microsatellite instability by immunohistochemistry and by PCR. The immunohistochemistry analysis demonstrated normal hMLH1, hMSH2 and hMSH6 protein expression. The PCR based assay showed MSI in 6 of 9 markers tested. Further testing for a mutation in hMSH2 was done on blood with a conformation sensitive gel electophoresis mutation scanning technique. Southern blot analysis was also performed and no mutations could be found in the hMSH2 gene.

After an extensive discussion with the patient and surgeon regarding his findings and the potential for a germ-line propensity for cancer, it was elected to proceed with a total coloectomy and formation of an ileostomy.

Pathology on the surgical specimen revealed the previous polypectomy site 3.7 cm from the pectinate line with no residual tumor found (Figure 5A). However, necrosis was found into the muscularis propria (Fig 5A-C, Muscularis Propria, Yellow "M"). Ten perirectal lymph nodes were all negative for metastatic disease. Two 4 mm tubular adenomas were also found in the resected specimen, one in the transverse colon the other in the descending colon. The patient had an uneventful postoperative course.


Discussion

Figure 5A

Figure 5B

Figure 5C

EUS is a valuable tool in the staging of rectal malignancies (1,2). A rather large literature body exists showing the utility of EUS in directing therapy of rectal cancer, particularly in determining whether or not trans anal local resection can be utilized for small tumors, or whether more aggressive neoadjuvant therapy is needed for advanced lesions (1-4).

Studies on the accuracy of EUS have focused primarily on the T and N staging of tumors at the time of diagnosis. The depth of invasion (T stage) is generally felt to be about 90% accurate for EUS, and for nodal status about 80% accurate (5).

Pitfalls regarding EUS staging involve many technical issues, such as position of the probe, endoluminal artifacts, peritumoral inflammation, desmoplastic changes, and post biopsy changes (6,7)

Inflammation, as occurs after polypectomy, can disrupt the echolayers of the bowel wall, and negatively impact EUS staging. To address the effect of polypectomy on staging, Kruskal et al. evaluated 18 patients who had malignant polyps and who were then staged by EUS for residual tumor (8). The accuracy of EUS was much less than what was seen in previous studies evaluating T-stage (5). Although Kruskal et al reported a sensitivity of 100% for finding residual disease, their specificity was only 44%. They still conclude that EUS is useful in staging surgery.

Our case visually demonstrates inflammatory artifact than mimics tumor. Had the EUS abnormalities been confined to the submucosa, one could have considered a trans anal approach to managing the positive margins of this endoscopically resected tumor. However, this case was somewhat complicated by the presence of a probable genetic cancer syndrome and patient wishes for an aggressive surgical approach.

This case illustrates a potential pitfall in staging rectal tumors following polypectomy. We recommend EUS staging be performed prior to polypectomy for potentially malignant rectal polyps for more accurate staging and to assess the feasability of endoscopic management. For polyps which have been removed and in which cancer has been found, one should consider marking the area with india ink and performing EUS after healing of the polypectomy ulcer.

References

1. Saitoh N, Okui K, Sarashina H, Suzuki M, Arai T, Nunomura M Evaluation of echographic diagnosis of rectal cancer using intrarectal ultrasonic examination Dis Colon Rectum 1986 Apr;29(4):234-42

2. Lindmark G, Elvin A, Pahlman L, Glimelius B. The value of endosonography in preoperative staging of rectal cancer Int J Colorectal Dis 1992 Sep;7(3):162-6

3. Marone P, Petrulio F, de Bellis M, Battista Rossi G, Tempesta A Role of endoscopic ultrasonography in the staging of rectal cancer: a retrospective study of 63 patients J Clin Gastroenterol 2000 Jun;30(4):420-4

4. Hildebrandt U, Feifel G Importance of endoscopic ultrasonography staging for treatment of rectal cancer Gastrointest Endosc Clin N Am 1995 Oct;5(4):843-9

5. Herzog U, von Flue M, Tondelli P, Schuppisser JP How accurate is endorectal ultrasound in the preoperative staging of rectal cancer Dis Colon Rectum 1993 Feb;36(2):127-34

6. Kruskal JB, Kane RA, Sentovich SM, Longmaid HE Pitfalls and sources of error in staging rectal cancer with endorectal us Radiographics 1997 May-Jun;17(3):609-26

7. Akasu T, Sugihara K, Moriya Y, Fujita S Limitations and pitfalls of transrectal ultrasonography for staging of rectal cancer Dis Colon Rectum 1997 Oct;40(10 Suppl):S10-5

8. Kruskal JB, Sentovich SM, Kane RA Staging of rectal cancer after polypectomy: usefulness of endorectal US Radiology 1999 Apr;211(1):31-5





Editorial Board:
Manoop S. Bhutani, M.D.
Galveston, TX
William R. Brugge, M.D.
Boston, MA
Peter R. McNally, D.O.
Denver, CO
Iqbal S. Sandhu, M.D.
Salt Lake City, UT
Thomas J. Savides, M.D.
San Diego, CA

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