Villous adenoma

WikiDoc Resources for Villous adenoma
Articles
Most recent articles on Villous adenoma Most cited articles on Villous adenoma Review articles on Villous adenoma Articles on Villous adenoma in N Eng J Med, Lancet, BMJ
Media
Powerpoint slides on Villous adenoma Images of Villous adenoma Photos of Villous adenoma Podcasts & MP3s on Villous adenoma Videos on Villous adenoma
Evidence Based Medicine
Cochrane Collaboration on Villous adenoma Bandolier on Villous adenoma TRIP on Villous adenoma
Clinical Trials
Ongoing Trials on Villous adenoma at Clinical Trials.gov Trial results on Villous adenoma Clinical Trials on Villous adenoma at Google
Guidelines / Policies / Govt
US National Guidelines Clearinghouse on Villous adenoma NICE Guidance on Villous adenoma NHS PRODIGY Guidance FDA on Villous adenoma CDC on Villous adenoma
Books
Books on Villous adenoma
News
Villous adenoma in the news Be alerted to news on Villous adenoma News trends on Villous adenoma
Commentary
Blogs on Villous adenoma
Definitions
Definitions of Villous adenoma
Patient Resources / Community
Patient resources on Villous adenoma Discussion groups on Villous adenoma Patient Handouts on Villous adenoma Directions to Hospitals Treating Villous adenoma Risk calculators and risk factors for Villous adenoma
Healthcare Provider Resources
Symptoms of Villous adenoma Causes & Risk Factors for Villous adenoma Diagnostic studies for Villous adenoma Treatment of Villous adenoma
Continuing Medical Education (CME)
CME Programs on Villous adenoma
International
Villous adenoma en Espanol Villous adenoma en Francais
Business
Villous adenoma in the Marketplace Patents on Villous adenoma
Experimental / Informatics
List of terms related to Villous adenoma

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Maria Fernanda Villarreal, M.D. [2]

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; it occurs most commonly in the colon. Villous adenoma may result in malignant (cancerous) transformation. Villous adenoma was first discovered by Helwig in 1946. 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, TP53, K-ras, and BAT-26. The prevalence of villous adenoma is approximately 3.5 per 100,000 individuals worldwide. The most potent risk factors in the development of villous adenoma include 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. Secondary prevention strategies include annual occult blood test and colonoscopy every ten years for patients above the age of 50.

Historical Perspective

Villous adenoma was first discovered by Helwig in 1946.

Classification

Gastrointestinal adenomas may be classified into 3 subtypes according to their histological appearance:

• Tubular
• Tubulovillous
• Villous

Villous adenoma can be classified into 4 types according to the gross appearance:

• Flat
• Sessile
• Pedunculated
• Depressed

Villous adenoma is classified into 2 types according to dysplasia:

• Low grade dysplasia
• High grade dysplasia

Pathophysiology

Pathogenesis

• Villous adenoma is a type of colonic poylp.
• The pathogenesis of villous adenoma is characterized by overgrowth of epithelial tissue with glandular characteristics.
• Dysplastic changes are present in the adenomas.
• Multiple genetic mutations result in the transition from normal mucosa to adenoma to severe dysplasia and finally to carcinoma
• Low grade or high-grade dysplasia, which indicates the level of maturation of the epithelium determine the progression of the adenoma.
• Features of low grade dysplasia are:
  • The cytological features include crowded, pseudo-stratification to early stratification of spindled or elongated nuclei which occupy the basal half of the cytoplasm.
  • Pleomorphism and atypical mitoses are absent.
  • The crypts maintain a resemblance to normal colon, without significant crowding, cribriform, or complex forms.The lesions are confined to the epithelial layer of crypts and lack invasion through the basement membrane into the lamina propria.
  • As there are no lymphatic vessels in the lamina propria, lesions with low grade dysplasia are not associated with metastasis.
• Features of high grade dysplasia are:
  • The cytological features include increased nucleus to cytoplasm ratio, more significant loss of polarity and nuclei with increasingly prominent nucleoli.
  • Significant pleomorphism, rounded nuclei, atypical mitoses, and significant loss of polarity.
  • The crypts are cribriform and crowded with back-to-back glandular tissue .
  • These adenomas have a significant risk of metasstasis as the lesions can invade into the lamina propria through basement membrane destruction.
• Villous adenoma can lead to adenocarcinoma of the colon.
• The progression of adenoma-to-carcinoma is dependent on the activation of oncogenes and inactivation of tumor suppresor genes.
• Multiple genetic mutations result in the transition from normal mucosa to adenoma to severe dysplasia and finally to carcinoma.
• The genes involved in adenoma formation are:
  • K-ras oncogene
  • Tumor suppresor p53 gene
  • APC gene on 5 chromosome associated with familial automatosis polyposis syndrome and Gardner syndome
  • STK11 (LBK1) gene, located on chromosome 19 associated with Peutz-Jeghers syndrome.
  • SMAD4 on chromosome 8 associated with juvenile polyposis syndrome.
• Villous adenomas may cause secretory diarrhea characterized by hypokalemia, chloride-rich stool, and metabolic alkalosis. Increased numbers of goblet cells and increased prostaglandin E2 are responsible for the diarrhea.

Colon adenoma By No machine-readable author provided. KGH assumed (based on copyright claims). - No machine-readable source provided. Own work assumed (based on copyright claims)., CC BY-SA 3.0, https://commons.wikimedia.org/w/index.php?curid=444694

Causes

The cause of villous adneoma is not yet identified.

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.

Age

• Patients of all age groups may develop villous adenoma but the risk increases with age.

Gender

• Males are more commonly affected with villous adenoma than females.

Race

• African Americans are more prone to develop villous adneoma.

Region

• Villous adenomas are common worldwide.

Risk Factors

Common risk factors in the development of villous adenoma include:

• Age more than 50 years.
• African American race
• Male sex
• Inflammatory bowel disease
• Alcohol abuse
• Obesity
• Lack of exercise
• Diet high in red meats and processed meats
• Low fiber intake
• Low calcium intake
• Low folate intake
• Type 2 diabetes mellitus
• 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.
• They are usually found accidentally on routine colonoscopic surveillance.
• Early clinical features may include flatulence, bloating, and abdominal pain.
• If left untreated, patients with villous adenoma may progress to develop colorectal cancer.
• The patients may have a previous history of colonic poylps.
• Family history of colon cancer or colon polyps.
• History of smoking.

Complications

Common complications of villous adenoma include:

• Gatsrointestinal Bleeding
• Intestinal obstruction
• Bowel torsion
• Progression to colorectal cancer.

Prognosis

• The prognosis of villous adenoma is generally good and the 5-year mortality is approximately 89%.
• Prognosis becomes poor with malignant transformation of the lesion.
• Multiple villous adenomas may suggest genetic disorders and prognosis is poor in these cases.

Diagnosis

Diagnostic study of choice

• Biopsy of the lesion is the diagnostic study of choice.
• Villous adenoma is detected on colonoscopy or sigmoidoscopy.

Symptoms

Villous adenoma is commonly asymptomatic but sometimes patients may present with the following symptoms:

• Flatulence
• Abdominal pain
• Constipation
• Diarrhea
• Cramping
• Blood in stools
• Weight loss
• Change in bowel habits
• Fatigue

Physical Examination

Patients with villous adenoma usually appear well but may have the following signs on exmaination.

• Pallor due to occult bleeding
• Abdominal tenderness
• Bright red blood on digital rectal examination
• Rectal mass on digital rectal examination

Laboratory Findings

Laboratory findings associated with villous adenoma are:

• Positive fecal occult blood test
• Hypokalemia.
• Anemia

Other diagnostic studies

On colonoscopy and sigmoidoscopy, villous adenoma is visualised as a polyp.

Alternative imaging studies include:

• CT colonography
• Video capsule endoscopy

Treatment

Medical Therapy

• There is no medical therapy for villous adenoma.
• Surgical removal of the adenoma is the mainstay of treatment.
• However, aspirin 75mg PO per day is recommended to prevent recurrence of the adenoma and progression to colorectal cancer.

Surgery

• Surgical removal is the mainstay of therapy for villous adenoma.
• The removal of adenoma is known as polypectomy and is done through colonoscopy.
• The removed adenoma is sent for biopsy.

{{#ev:youtube|ClgRkyhaJZw}}

Prevention

Primary Prevention

Effective measures for the primary prevention of villous adenoma include periodic screening for patients with family history of familial adenomatous polyposis.

Secondary Prevention

Secondary prevention strategies include annual occult blood test and colonoscopy every ten years for patients above the age of 50.