CC BY-NC-ND 4.0 · Endosc Int Open 2019; 07(11): E1549-E1562
DOI: 10.1055/a-0998-3958
Original article
Owner and Copyright © Georg Thieme Verlag KG 2019

Video anoscopy: results of routine anal examination during colonoscopies

Alexandre Gomes
Department of Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
,
Maurício Kazuyoshi Minata
Department of Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
,
José Jukemura
Department of Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
,
Eduardo Guimarães Hourneaux de Moura
Department of Gastroenterology, Faculdade de Medicina da Universidade de São Paulo, São Paulo, Brazil
› Institutsangaben
Weitere Informationen

Corresponding author

Alexandre Gomes, MD, MSc
Department of Gastroenterology
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Rua Dr. Luiz Garcia Duarte 125
18047-599 Sorocaba – São Paulo
Brasil   
Fax: +55-15-32113601   

Publikationsverlauf

submitted 18. März 2019

accepted after revision 22. Juli 2019

Publikationsdatum:
11. November 2019 (online)

 

Abstract

Background and study aims Anal examination and video anoscopy (VA) are rarely performed during colonoscopies. The aim of this study is to demonstrate that anal examination and VA provide important information in all routine colonoscopies.

Patients and methods A cross-sectional study was conducted on 12,151 patients screened by VA which were performed during routine outpatient colonoscopy between 2006 and 2018. The aspects studied were: normal examination; hemorrhoidal disease; thrombosed hemorrhoids; anal fissure; perianal Crohn’s Disease; perianal fistula; condyloma; polyps; neoplasms; stenosis; bleeding.

Results Of the colonoscopies performed on 12,151 patients, 9,364 cases (77.06 %) presented some alterations. Internal I degree hemorrhoids (5911 – 48.65 %); internal hemorrhoids of II, III and IV degrees (2362 – 19.44 %); thrombosed hemorrhoids (120 – 0.99 %); bleeding (56 – 0.46 %); fissure (415 – 3.42 %); perianal fistula (42 – 0.35 %); perianal Crohn’s Disease (34 – 0.28 %); condylomas (18 – 0.15 %); anal stenosis (30 – 0.25 %); other findings (310 – 2.55 %); polyps (62 – 0.51 %), one of which was adenomatous with high-grade dysplasia; four cases of anal canal neoplasia (0.03 %): two cases of squamous cell carcinoma and two cases of adenocarcinoma.

Conclusion The association of routine video anoscopy during colonoscopy improved diagnosis of neoplastic anal lesions, allowed correct classification of the degree of hemorrhoidal disease, helped to confirm the bleeding site and detected other anal pathologies. The main findings were hemorrhoidal diseases, fissures and perianal fistulas. The study suggests that VA should be used in all colonoscopies.


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Introduction

Assessment of the anal canal and perianal region is part of an adequate screening for neoplasias and evaluation of intestinal bleeding sources [1] [2]. Although colonoscopy is a recognized diagnostic and therapeutic method for investigation of colorectal diseases, it presents limited visualization and evaluation of the anal region. Some maneuvers may be used to improve evaluation of the lower rectum and anal canal by colonoscopy, such as rectal retroflexion [3] [4]. Even with use of this technique, lesions may go unnoticed and many disorders of the anal canal may not be detected [5] [6] [7] [8] [9] [10].

Anoscopy is the gold standard for anal canal evaluation, but is often neglected in medical practice [2] [9]. Standard anoscopy is the one performed with use of an anoscope and direct visualization of the anal region, usually without sedation and without bowel preparation [11]. However, sometimes anoscopy without sedation can become an embarrassing, uncomfortable and painful situation. It can be impossible if the patient has anal pain or improper preparation. In addition, it has a more limited and distant view, with the face of the operator exposed to the fecal spray.

In 1995 an examination technique called video anoscopy (VA) was described by Lazas et al. [9]. Examination of the anal canal was performed with an anoscope and visualized by video sigmoidoscope, without sedation. Performing VA during colonoscopy, with the patient under sedation and with bowel preparation, may improve visualization of normal and altered structures by way of high-quality images, thus increasing sensitivity in detection of anal disorders ([Fig. 1]).

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Fig. 1 Video anoscopy during colonoscopy.

Studies available in the literature on video anoscopy during colonoscopies in detection of diseases of the anal canal are scarce. The purpose of our study was to access the spectrum of diagnoses, prevalence of anal disorders, and importance of anal examination made by VA in colonoscopies in evaluation of anal diseases.


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Patients and methods

This is a single-center cross-sectional study of patients who were referred for routine colonoscopy and were systematically evaluated with inclusion of anal examination by video anoscopy. Data were retrospectively analyzed from consecutive patients who underwent routine colonoscopy from October 25, 2006 to September 10, 2018. The study was approved by the local Ethics Committee.

All patients in the study underwent bowel preparation. An admission record was filled in with patient data and history of previous surgeries. The equipment used was a Pentax standard videocoloscope (Pentax Corporation, Tokyo, Japan) or Fujinon (Fujifilm, Tokyo, Japan) and the transparent disposable plastic anoscope (Plastic Way or Kolplast).

Patients were monitored throughout the procedure, with heart rate, blood pressure, and oximetry parameters. After conscious sedation, they were submitted to VA and colonoscopy, by the same professional.

Patients underwent a digital rectal examination and the colonoscope was inserted into the rectum with aspiration of the liquid contents. An evaluation was performed with straight withdrawal of the colonoscope, visualizing the rectum, dentate line and anal canal. Afterwards, the anoscope was inserted, the anal canal and perianal region were evaluated using the videocolonoscope and the results recorded. Biopsies and polypectomies were performed if needed. After this evaluation, the colonoscopy was performed.

Reports of the exams and the images obtained were recorded and saved in a database (OCRAM, SP system). This system was used to record VA images and compose the respective reports during the study period. The colonoscopy report format with anal examination described in a separate item allowed the search for pre-established patterns. The results were grouped separately, dividing the male and female patients and classified by 10-year age groups. Reports that presented non-standardized descriptions were analyzed individually by the images, and then grouped.

Repeated exams on different dates on the same patient were excluded and thus remained the single most relevant report. The resulting patients who were analyzed and evaluated displayed the following diagnoses: normal examination; hemorrhoidal disease; thrombosed hemorrhoids; anal fissure; perianal Crohnʼs Disease (pCD); perianal fistula; condyloma; polyps; neoplasms; anal stenosis; bleeding ([Fig. 2]). The Goligher classification for hemorrhoids was used [12].

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Fig. 2 a Internal hemorrhoids grade II. b Thrombosed hemorrhoids. c hemorrhoids with active bleeding. d Anal ulceration in Crohnʼs Disease. e Fissure. f, g Perianal Crohn's disease. h External orifice in perianal fistula. i Purulent discharge in perianal fistula. j Squamous cell carcinoma of the anal canal. k Adenocarcinoma of the anal canal. l Condyloma acuminata (HPV). m, n, o Polyps.

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Results

We retrospectively analyzed findings from 16,132 exams in 12,151 consecutive patients. A total of 12,151 VAs were analyzed. The minimum age was 4 years and the maximum age was 94 years. The average age was 48.57 and the median was 49, being 7,196 female (59 %), and 4,955 male (41 %), divided into 10-year age groups ([Fig. 3a – p]). From this, 2787 video anoscopies were normal and 9364 cases presented some alterations ([Table 1]).

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Fig. 3 Graphs. Findings of the video anoscopies in female and male groups divided by gender and classified by 10-year age groups. a VA divided by gender.
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Fig. 3b Bar chart of the findings and number of cases of the video anoscopies.
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Fig. 3c Pie chart of the findings and number of cases of the video anoscopies.
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Fig. 3d Total of VA divided by gender and classified by 10-year age groups.
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Fig. 3e Normal VA divided by gender and classified by 10-year age groups.
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Fig. 3f Hemorrhoids divided by gender and classified by 10-year age groups.
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Fig. 3g Anal fissure divided by gender and classified by 10-year age groups.
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Fig. 3h Polyps divided by gender and classified by 10-year age groups.
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Fig. 3i Perianal fistula divided by gender and classified by 10-year age groups.
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Fig. 3j Thrombosed hemorrhois divided by gender and classified by 10-year age groups.
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Fig. 3k Anal stenosis divided by gender and classified by 10-year age groups.
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Fig. 3l Perianal Crohn’s Disease divided by gender and classified by 10-year age groups.
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Fig. 3m Condylomas divided by gender and classified by 10-year age groups.
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Fig. 3n Bleeding divided by gender and classified by 10-year age groups.
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Fig. 3o Neoplasm divided by gender and classified by 10-year age groups.
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Fig. 3p Other divided by gender and classified by 10-year age groups.
Table 1

Findings of the video anoscopies in female and male groups divided by gender and classified by 10-year age groups.

Min. Age

 4

Video anoscopies

Max. Age

94

2006 to 2018

Average

48,57

12151

Median

49

Mode

51

Male

Age group

[0 – 10]

[10 – 20]

[20 – 30]

[30 – 40]

[40 – 50]

[50 – 60]

[60 – 70]

 > 70

TOTAL

Anal examination

6

 92

463

 863

1138

1236

 775

382

4955

Normal

6

 60

215

 223

 178

 146

  85

 86

 999

Hemorrhoids internal/total

0

 13

165

 522

 843

 997

 635

273

3448

Hemorrhoids grade I

0

 12

139

 414

 585

 586

 324

140

2200

Hemorrhoids grade II

0

  1

 26

 104

 252

 403

 302

128

1216

Hemorrhoids grade III

0

  0

  0

   4

   6

   8

   9

  5

  32

Hemorrhoids grade IV

0

  0

  0

   0

   0

   0

   0

  0

   0

Anal fissure

0

  9

 38

  50

  37

  35

   9

  5

 183

Polyps

0

  0

  4

   7

   8

   5

   9

  4

  37

Perianal fistula

0

  0

  7

   9

   9

   6

   2

  0

  33

Thrombosed hemorrhoids

0

  5

  8

  20

  15

   8

   2

  1

  59

Anal stenosis

0

  0

  0

   1

   4

   2

   3

  1

  11

Perianal Crohnʼs disease

0

  1

  5

   8

   4

   1

   3

  0

  22

Condyloma

0

  1

  9

   1

   1

   0

   0

  0

  12

Bleeding

0

  2

  3

   9

   7

   8

   0

  2

  31

Neoplasm

0

  0

  0

   0

   0

   0

   3

  0

   3

Other

0

  1

 12

  16

  26

  29

  23

 10

 117

Female

Age group

[0 – 10]

[10 – 20]

[20 – 30]

[30 – 40]

[40 – 50]

[50 – 60]

[60 – 70]

 > 70

TOTAL

Anal examination

7

130

830

1329

1669

1722

1045

464

7196

Normal

5

 89

435

 441

 338

 248

 142

 90

1788

Hemorrhoids internal/total

0

 24

279

 753

1198

1366

 855

350

4825

Hemorrhoids grade I

0

 23

247

 656

 969

 997

 595

224

3711

Hemorrhoids grade II

0

  1

 31

  95

 216

 353

 250

117

1063

Hemorrhoids grade III

0

  0

  1

   2

  12

  16

  10

  6

  47

Hemorrhoids grade IV

0

  0

  0

   0

   1

   0

   0

  3

   4

Anal fissure

2

 10

 66

  58

  47

  35

  11

  3

 232

Polyps

0

  0

  3

   4

   6

   5

   6

  1

  25

Perianal fistula

0

  0

  2

   0

   4

   2

   0

  1

   9

Thrombosed hemorrhoids

0

  0

 10

  20

  15

  11

   4

  1

  61

Anal stenosis

0

  0

  2

   3

   1

   4

   4

  5

  19

Perianal Crohnʼs disease

0

  0

  6

   3

   0

   0

   1

  2

  12

Condyloma

0

  1

  2

   1

   2

   0

   0

  0

   6

Bleeding

0

  0

  4

   4

   7

   5

   4

  1

  25

Neoplasm

0

  0

  0

   0

   0

   0

   0

  1

   1

Other

0

  6

 23

  42

  43

  45

 23

 11

 193

Hemorrhoidal disease was found in 8,273 cases (68.08 %) and separated according to the findings of hemorrhoids of I, II, III and IV degrees. Hemorrhoidal bleeding at the time of examination was noticed in 56 cases (0.46 %) and thrombosed hemorrhoids in 120 cases (0.99 %).

A total of 415 patients (3.42 %) were found to have fissures. Perianal Crohn’s disease was noticed in 34 patients (0.28 % of 7.57 %), including fissures and ulcerated lesions in the anal canal.

Forty-two cases of perianal fistula (0.35 %) were identified by the external orifice and the mucus or purulent discharge at the time of video anoscopy. There was a predominance of males (33 cases – 78.57 %) over the female group (9 cases – 21.43 %).

Thirty cases (0.25 %) of symptomatic anal stenosis were observed, of which 36.66 % were male and 63.33 % were female.

We found 18 cases of condylomatous lesions (0,15 %). Males predominated with 12 cases (66.66 %) found, and in the female group six cases (33.33 %).

There were 310 cases (2.55 %) with small changes of little clinical importance and that were grouped as other perianal disorders. These findings correspond to cases of skin tags, perianal dermatitis, mucosal prolapses and anal sphincteric hypotonia in digital rectal examination.

In 62 patients, polyps were found in the anal canal, of which 58 were fibroepithelial, one telangiectatic granuloma, two cases were hyperplastic polyps, and one polyp was tubulovillous adenoma with high grade dysplasia. The rate of detection of neoplasms with the anal exam in the study was 0.03 % (4 cases), two cases of squamous cell carcinoma and two cases of adenocarcinoma.


#

Discussion

Many examiners evaluate the anal region by performing straight withdrawal (SW) of the colonoscope and rectal retroflexion (RR). However, evaluation of the degree of hemorrhoidal disease is facilitated with use of the anoscope. The SW does not accurately visualize the hemorrhoidal columns nor its prolapse. In the rectal retroflex maneuver there is a need for complete air insufflation and this leads to hemorrhoidal venous plexus collapse, impairing evaluation ([Video 1]). For visualization of anal fissures, it is also essential to use the anoscope, which sometimes becomes impossible without sedation. A prospective, multicenter, blinded study by Tellez-Ávilla et al. showed that RR during colonoscopy has limited effect and little impact on diagnosis and therapy [13]. Two prospective studies have shown that anoscopy was superior to RR in detection of hemorrhoids [1] [2] [14]. Kelly [2] showed that the SW had a disease detection rate of 54 %, RR of 78 % and VA 99 % [2]. Harish [1] showed that VA detected significantly more hemorrhoids than RR.

Video 1 Video anoscopy during colonoscopy.


Qualität:

Rectal bleeding is always a symptom of alarm and countless exams are done for fear of a serious condition going undetected [15]. Patients with hemorrhoids and painless bleeding are referred for colonoscopy to exclude other causes of bleeding such as neoplasia. Hemorrhoids are by far the commonest cause of rectal bleeding [16] [17]. An appropriate examination of the anal canal is mandatory in evaluation of each patient with a history of rectal bleeding to avoid misdiagnosis, unnecessary exams, and inadequate treatment [1]. Rectal retroflexion (RR) is often used to evaluate hemorrhoids, but this technique has little sensitivity [1] [5]. One study demonstrated that the gain related to the finding of lesions identified with RR was from 2 % to 8 % [13]. VA can determine the cause of bleeding if it is of anal origin. In this study, it was observed that in 56 cases, the origin of anal bleeding was identified at the time of colonoscopy, thanks to anal examination with VA and to visualization of the exact site of active bleeding. There were 123 cases (0.76 %) that included cases of internal and external thrombosed hemorrhoids.

Anal fissures are the most common causes of anal pain and typical symptoms include pain and bleeding [18]. Some patients may experience severe discomfort during the examination and anoscopies are not always well tolerated. The VA made during the colonoscopy, with the patient sedated, greatly facilitates diagnosis of anal fissure. [Video 1] shows the difference in anal fissure viewing by SW, RR and VA. If anal fissure develops in atypical sites, other diseases, such as Crohn's Disease (CD), ulcerative colitis, syphilis, tuberculosis, leukemia, HIV-associated lesions, and anal canal neoplasms should be considered. Visualization of the anal fissure is greatly facilitated by use of the transparent anoscope in conjunction with the colonoscope, as well as sedation with propofol, which allows adequate and painless examination, making the diagnosis possible in all cases. Patients with Crohn's disease have complex perianal lesions that need to be evaluated during colonoscopy because they require specific treatment. Primary lesions include Crohn’s fissures and cavitating perianal ulcers. Secondary lesions include deep abscesses fistulas and strictures [19]. The lowest 1 cm of rectal mucosa may be affected by localized caviting ulceration and stricture, both of which are very characteristic of pCD [20]. Presence of proctitis, ulceration, fistula or stricture of the anal canal is an important component to determine an optimal management strategy [21].

Anal abscesses and fistulas are, respectively, the acute and chronic manifestations of the same process [18]. Symptoms of the perianal fistula are drainage of secretion in the perianal region, pain, local swelling and presence of an orifice in the skin near the anal border, from where the secretion exits [15]. Perianal fistulas are the most common manifestation of fistulizing CD, developing in 20 % of Crohn’s patients and recurring in approximately 30 % of cases [21]. Exam under anesthesia remains the standard for diagnosis and classification of perianal fistula with an accuracy of up to 90 % when diagnosing pCD [22]. Visualization of the external orifice and the purulent secretion discharge is facilitated by use of the anoscope, which compresses the anal canal and promotes its drainage.

Malignant tumors of the anus and anal canal are rare, with carcinoma of the anal canal being three times more common than that of the perianal skin. Both are uncommon entities and represent less than 2 % of all colon, rectum, and anus carcinomas [23] [24] [25]. Although anal cancer is relatively uncommon, incidence rates are increasing in certain risk populations, such as those with human papillomavirus or AIDS (HIV) [26] [27]. The diagnosis of precursor lesion and anal cancer requires an adequate examination [25] [26].

It is important to identify tumors that grow in the anal canal of those of the perianal skin, due to the peculiar biological behaviors and different therapeutics [18]. Squamous cell carcinoma of the anal canal is usually an ulcerated or fissured lesion with raised or hardened edges. Proctological examination may reveal a hardened, ulcerated hemorrhagic mass in the anal canal and lower rectum [23] [28]. Any suspicious lesion around the anus should be biopsied. The concomitance of anal canal neoplasia with benign diseases is common and some lesions are easily confused with these conditions. Its clinical manifestations are uncharacteristic and often attributed to hemorrhoidal disease, thus delaying correct diagnosis.

Anal cancer usually presents pain, anal mass, and bleeding; however, in 20 % of cases there are no symptoms [29]. Careful anal examination allows these tumors to be diagnosed early, even with small dimensions, allowing better prognosis [30]. The most common aspect is the fissure or ulcerated lesion with raised edges, irregular, granular, hard, painful, and bleeding. Differential diagnosis with chronic anal fissure can be performed due to absence of post-evacuation pain (typical of the fissure) and the atypical location of the ulceration, since in 90 % of the cases the anal fissure is posterior and the neoplasm can occur in any position.

Although uncommon, undiagnosed anal canal cancers and the missed chance of an early diagnosis during a routine colonoscopy can be disastrous for the patient and could also bring a malpractice lawsuit to the practitioner who fails to diagnose an initial malignant lesion. The rate of detection of neoplasms with the anal exam in our study was 0.03 % (4 cases), two cases of squamous cell carcinoma and two cases of adenocarcinoma. In 62 patients, polyps were found in the anal canal , but only one polyp was neoplastic. We found 18 cases of condylomatous lesions (HPV), with male predominance of 12 cases (66.66 %), and in the female group six cases (33.33 %). The fragments for analysis were collected by biopsy or with application of local anesthetic and removal with surgical scissors.

During colonoscopy VA becomes easier, with high-quality images that improve visualization of normal and altered structures, resulting in improved sensitivity over the standard anoscopy in detection of anal disorders. In addition, it is a practice that interferes little in the dynamics of the examination, is performed in a few seconds, reduces exposure of fecal residues to the operator, and has a low cost. With the increased number of colonoscopies performed due to the routine indication for prevention of colorectal cancer, patients with few or even no complaints could have earlier diagnoses of anal lesions.

An analysis with this significant number of cases may help to understand the importance of anal canal evaluation during colonoscopy and correct identification of the anal diseases and then referral of cases for appropriate specialized treatment. With proper training, it is possible to make a good evaluation of the anal region and to include this information in the reports.


#

Conclusion

The association of routine video anoscopy during colonoscopy improved the diagnosis of the neoplastic anal lesions, allowed correct classification of the degree of hemorrhoidal disease, helped to confirm the bleeding site and detected other anal pathologies. The main findings were hemorrhoidal diseases, fissures and perianal fistulas. The study suggests that VA should be used in all colonoscopies.


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Competing interests

None

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  • 22 Kelley KA, Kaur T, Tsikitis VL. Perianal Crohn’s disease: challenges and solutions. Clin Exp Gastroenterol 2017; 10: 39-46
  • 23 Albuquerque A. High-resolution anoscopy: Unchartered territory for gastroenterologists?. World J Gastrointest Endosc 2015; 7: 1083-1087
  • 24 Uronis HE, Bendell JC. Anal cancer: an overview. Oncologist 2007; 12: 524-534
  • 25 Magalhães M. Anal canal squamous carcinoma. J Coloproctol 2017; 37: 72-79
  • 26 Grulich AE, Poynten IM, Machalek DA. et al. The epidemiology of anal cancer. Sex Health 2012; 9: 504-508
  • 27 Ryan DP, Compton CC, Mayer RJ. Carcinoma of the anal canal. N Engl J Med 2000; 342: 792-800
  • 28 Tanaka A, Sadahiro S, Suzuki T. et al. Comparisons of rigid proctoscopy, flexible colonoscopy, and digital rectal examination for determining the localization of rectal cancers. Dis Colon Rectum 2018; 61: 202-206
  • 29 Abunassar M, Reinders J, Jonker DJ. et al. Review of anal cancer patients at the Ottawa hospital. Eur J Surg Oncol 2015; 41: 653-658
  • 30 Wells JS, Holstad MM, Thomas T. et al. An integrative review of guidelines for anal cancer screening in HIV-infected persons. AIDS Patient Care STDS 2014; 28: 350-357

Corresponding author

Alexandre Gomes, MD, MSc
Department of Gastroenterology
Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo
Rua Dr. Luiz Garcia Duarte 125
18047-599 Sorocaba – São Paulo
Brasil   
Fax: +55-15-32113601   

  • References

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  • 21 Gecse KB, Bemelman W, Kamm MA. et al. A global consensus on the classification, diagnosis and multidisciplinary treatment of perianal fistulising Crohnʼs disease. Gut 2014; 63: 1381-1392
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  • 24 Uronis HE, Bendell JC. Anal cancer: an overview. Oncologist 2007; 12: 524-534
  • 25 Magalhães M. Anal canal squamous carcinoma. J Coloproctol 2017; 37: 72-79
  • 26 Grulich AE, Poynten IM, Machalek DA. et al. The epidemiology of anal cancer. Sex Health 2012; 9: 504-508
  • 27 Ryan DP, Compton CC, Mayer RJ. Carcinoma of the anal canal. N Engl J Med 2000; 342: 792-800
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Fig. 1 Video anoscopy during colonoscopy.
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Fig. 2 a Internal hemorrhoids grade II. b Thrombosed hemorrhoids. c hemorrhoids with active bleeding. d Anal ulceration in Crohnʼs Disease. e Fissure. f, g Perianal Crohn's disease. h External orifice in perianal fistula. i Purulent discharge in perianal fistula. j Squamous cell carcinoma of the anal canal. k Adenocarcinoma of the anal canal. l Condyloma acuminata (HPV). m, n, o Polyps.
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Fig. 3 Graphs. Findings of the video anoscopies in female and male groups divided by gender and classified by 10-year age groups. a VA divided by gender.
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Fig. 3b Bar chart of the findings and number of cases of the video anoscopies.
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Fig. 3c Pie chart of the findings and number of cases of the video anoscopies.
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Fig. 3d Total of VA divided by gender and classified by 10-year age groups.
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Fig. 3e Normal VA divided by gender and classified by 10-year age groups.
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Fig. 3f Hemorrhoids divided by gender and classified by 10-year age groups.
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Fig. 3g Anal fissure divided by gender and classified by 10-year age groups.
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Fig. 3h Polyps divided by gender and classified by 10-year age groups.
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Fig. 3i Perianal fistula divided by gender and classified by 10-year age groups.
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Fig. 3j Thrombosed hemorrhois divided by gender and classified by 10-year age groups.
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Fig. 3k Anal stenosis divided by gender and classified by 10-year age groups.
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Fig. 3l Perianal Crohn’s Disease divided by gender and classified by 10-year age groups.
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Fig. 3m Condylomas divided by gender and classified by 10-year age groups.
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Fig. 3n Bleeding divided by gender and classified by 10-year age groups.
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Fig. 3o Neoplasm divided by gender and classified by 10-year age groups.
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Fig. 3p Other divided by gender and classified by 10-year age groups.