Villous adenoma: Difference between revisions
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*[[APC gene]] | *[[APC gene]] | ||
*[[TP53|TP53 gene]] | *[[TP53|TP53 gene]] | ||
*[[ | *[[KRAS]] gene | ||
*BAT-26 gene | *BAT-26 gene | ||
Revision as of 22:42, 17 August 2016
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]; Tarek Nafee, M.D. [3]
Synonyms and keywords: Adenomatous polyps; VA; TVA
Overview
Villous adenoma (also known as adenomatous polyp) is a type of polyp that grows in the colon and other places in the gastrointestinal tract and may have a malignant (cancerous) transformation.[1] Villous adenoma was first discovered by Helwig in 1946.[2] According to the World Health Organization, villous adenoma can be classified into 3 groups: tubular, tubulovillous, and villous (most common). Villous adenoma arises from epithelial tissue, which is normally part of the lining of the colon. The estimated risk of malignancy among villous adenomas is between 15 and 25%. Genes associated in the development of villous adenoma, include: APC gene, TP53 gene, K-ras gene, and BAT-26 gene. The prevalence of villous adenoma is approximately 3.5 per 100,000 individuals worldwide. The most important risk factor in the development of villous adenoma is familiar syndromes (e.g. Turcot syndrome, juvenile polyposis syndrome, and Cowden disease). Surgical removal is the mainstay of therapy for villous adenoma. Cautery snare in conjunction with exploratory colonoscopy is the most common approach to the treatment of villous adenoma. Effective measures for the primary prevention of villous adenoma include periodical screening for patients with family history of familial adenomatous polyposis. According to the guidelines established by the American Cancer Society, individuals who reach the age of 50 should perform an occult blood test yearly.
Historical Perspective
Villous adenoma was first discovered by Helwig in 1946.[2]
Classification
Villous adenoma may be classified according to the World Health Organization into 3 groups:[3]
- Tubular
- Tubulovillous
- Villous (most common)
Pathophysiology
Pathogenesis
The pathogenesis of villous adenoma is characterized by:[3] Villous adenoma arises from overgrowth of epithelial tissue with glandular characteristics.
Genetics
Genes associated with the development of villous adenoma include:[3]
Gross Pathology
On gross pathology, characteristic findings of villous adenoma include:[3]
- Polypoid or sessile mass
- Cauliflower-like in appearance
Microscopic Pathology
On microscopic histopathological analysis, characteristic findings of villous adenoma include:
- Nuclear changes at the surface of the mucosa
- Cigar-shaped (elongated) nucleus (length:width > 3:1) with nuclear hyperchromasia
- Large round nuclei
- Nuclear crowding
- Positive Ki-67
Causes
The most important cause of villous adenoma is familial adenomatous polyposis.
Differentiating Villous Adenoma from Other Diseases
- Villous adenoma must be differentiated from other diseases that cause abnormal growth of tissue projecting from a mucous membrane such as:
- Colorectal cancer
- Inflammatory fibroid polyp
Epidemiology and Demographics
Prevalence
The prevalence of villous adenoma is approximately 3.5 per 100,000 individuals worldwide. The prevalence of adenomas increases with age.
Age
Patients of all age groups may develop villous adenoma.
Gender
Males are more commonly affected with villous adenoma than females.
Race
Villous adenoma more commonly affects individuals of the Caucasian race.
Risk Factors
Common risk factors in the development of villous adenoma, include:
- Familial adenomatous polyposis
- Peutz–Jeghers syndrome
- Turcot syndrome
- Juvenile polyposis syndrome
- Cowden disease
- Bannayan–Riley–Ruvalcaba syndrome (Bannayan-Zonana syndrome)
- Gardner's syndrome
Natural History, Complications and Prognosis
Natural History
The majority of patients with villous adenoma remain asymptomatic for years. Early clinical features may include flatulence, bloating, and abdominal pain. If left untreated, patients with villous adenoma may progress to develop colorectal cancer.[3]
Complications
Common complications of villous adenoma include:
- Bleeding
- Obstruction
- Bowel torsion
Prognosis
Prognosis is generally good and the 5-year mortality of patients with villous adenoma is approximately 89%. Prognosis becomes poorer with malignant transformation of the lesion. The estimated risk of malignant transformation of villous adenoma is from 15% to 20%.
Diagnosis
Symptoms
Villous adenoma is usually asymptomatic. Villous adenoma symptoms are often non-specific. Symptoms of villous adenoma may include:
- Flatulence
- Abdominal pain
- Constipation
- Diarrhea
- Cramping
Physical Examination
Patients with villous adenoma usually are well-appearing. Physical examination findings are often non-specific. Physical examination may demonstrate:
- Rectal bleeding
- Rectal mass
- Pencil-thin stools
Laboratory Findings
There are no specific laboratory findings associated with villous adenoma. In some cases, patients with villous adenoma may demonstrate hypokalemia.[4]
Imaging and Diagnostic Findings
Colonoscopy is the diagnostic modality of choice for villous adenoma. On colonoscopy, characteristic findings of villous adenoma include:[3]
- A sessile polyp
- Size can range from 0.5 cm to 5 cm
Other imaging studies include:
- Computed tomographic colonography
- Video capsule endoscopy (less specific)
Treatment
Medical Therapy
There is no treatment for villous adenoma; the mainstay of therapy is surgical removal.
Surgery
Surgical removal is the mainstay of therapy for villous adenoma. Colonoscopy is both diagnostic and therapeutic. Cautery snare in conjunction with exploratory colonoscopy is the most common approach to both the diagnosis and treatment of villous adenoma.[3]
Prevention
Effective measures for the primary prevention of villous adenoma include periodic screening for patients with family history of familial adenomatous polyposis. According to the guidelines established by the American Cancer Society, individuals who reach the age of 50 should perform an occult blood test yearly, a colonoscopy every 10 years, or a flexible sigmoidoscopy every 3 to 5 years. Once diagnosed and successfully treated, patients with villous adenoma are followed-up every 12 to 24 months.
References
- ↑ Villous adenoma
- ↑ 2.0 2.1 Helwig E.B. Adenoma of the large bowel in children. . American Journal of Diseases in Children. 1946;72:289–95
- ↑ 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Osifo OD, Akhiwu W, Efobi CA (2009). "Small intestinal tubulovillous adenoma--case report and literature review". Niger J Clin Pract. 12 (2): 205–7. PMID 19764676.
- ↑ Villous adenoma. Wikipedia. https://en.wikipedia.org/wiki/Villous_adenoma Accessed on May 3, 2016