Villous adenoma
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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 gastrointestinal tract and commonly in the colon. Villous adenoma may result in malignant (cancerous) transformation.[1] Villous adenoma was first discovered by Helwig in 1946.[2] According to the World Health Organization, villous adenoma may be classified into tubular, tubulovillous, and villous (most common) subtypes. Villous adenoma arises from epithelial tissue, which is normally part of the lining of the colon. The estimated risk of malignant transformation among villous adenomas is between 15% and 25%. Genes associated with 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 potent risk factor in the development of villous adenoma are familial syndromes such as Turcot syndrome, juvenile polyposis syndrome, and Cowden disease). Surgical removal is the mainstay of therapy for villous adenoma. Exploratory colonoscopy and cautery snare is the most common approach to the diagnosis and treatment of villous adenoma. Effective measures for the primary prevention of villous adenoma include periodic screening of 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 undergo 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 overgrowth of epithelial tissue with glandular characteristics.[3]
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
Villous adenomas are commonly idiopathic. The most common known 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 caucasians.
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
The prognosis of villous adenoma is generally good and the 5-year mortality 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:
Physical Examination
Patients with villous adenoma commonly appear well. 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 positive fecal occult blood test or 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:
- CT colonography
- Video capsule endoscopy (less specific)
Treatment
Medical Therapy
There is no medical 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