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A carcinoma that arises from the hepatocytes or intrahepatic bile ducts. The main subtypes are hepatocellular carcinoma (hepatoma) and cholangiocarcinoma.
APC-associated polyposis conditions include classic familial adenomatous polyposis (FAP), attenuated FAP, and gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS). FAP In individuals with classic FAP, colorectal adenomatous polyps begin to appear in the second and third decade; the average age of polyp diagnosis is 16 years (range 7-36 years) . By age 35 years, 95% of individuals with FAP have polyps. Once they appear, the polyps rapidly increase in number; when colonic expression is fully developed, hundreds to thousands of colonic adenomatous polyps are typically observed. Without colectomy, colorectal cancer (CRC) is essentially inevitable. The average age of CRC diagnosis in untreated individuals is 39 years (range 34-43 years); 7% of untreated individuals with FAP develop CRC by age 21 years, 87% by 45 years, and 93% by 50 years. Although rare, asymptomatic individuals in their 50s have been reported. Inter- and intrafamilial phenotypic variability are common . Attenuated FAP is characterized by fewer colonic polyps (average of 30 polyps) than classic FAP but a significant risk for CRC. According to the international collaborative study by , attenuated FAP was clinically defined as individuals with ≤100 colorectal adenomatous polyps at age ≥25 years. Polyps tend to occur more proximally in the colon than in classic FAP. The average age of CRC diagnosis in individuals with attenuated FAP is 50 to 55 years – ten to 15 years later than in classic FAP, but earlier than in those with sporadically occurring CRC . The cumulative risk for CRC by age 80 years in attenuated FAP is estimated at 70% . Other Features Variably Present in FAP Table 2. Lifetime Risk for Extracolonic Cancer in Familial Adenomatous Polyposis
Site | Type of Cancer | Lifetime Risk for Cancer |
|---|---|---|
Small bowel: duodenum (most often periampullary region) | Adenocarcinoma, carcinoma | 4%-12% |
Small bowel: distal to the duodenum | Carcinoma | Rare |
Pancreas | Adenocarcinoma | ~1% |
Thyroid | Papillary thyroid carcinoma | 1%-12% |
CNS | Usually medulloblastoma | ~1% |
Liver | Hepatoblastoma | 1.6% |
Bile ducts | Adenocarcinoma | Low, but |
Stomach | Adenocarcinoma | 1.3% in Western cultures since 2016 Small-bowel polyps and cancer. Adenomatous polyps of the duodenum, observed in 50%-90% of individuals with FAP, are commonly found in the second and third portions of the duodenum and to a variable degree in the jejunum or ileum . |
Source: GeneReviews — "APC-Associated Polyposis Conditions"
The National Comprehensive Cancer Network (NCCN) has published an algorithm for consideration of the diagnosis of both familial adenomatous polyposis (FAP) and attenuated FAP (full text). These guidelines include recommendations for genetic testing of APC. Consensus guidelines specific for gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) are not yet available. According to the NCCN guidelines, an APC-associated polyposis condition should be suspected in individuals with any of the following clinical features:
Source: GeneReviews — "APC-Associated Polyposis Conditions"
Hereditary Disorders to Consider in the Differential Diagnosis APC-associated polyposis conditions may be distinguished from other inherited colorectal cancer conditions and other gastrointestinal polyposis syndromes by molecular genetic testing, histopathologic findings, and phenotypic characteristics. Table 4. Selected Hereditary Polyposis and Colorectal Cancer Syndromes in the Differential Diagnosis of APC-Associated Polyposis Conditions
Gene(s) / Genetic Mechanism | Disorder | MOI | Comment |
|---|---|---|---|
15q15.3q22.1 duplication1BMPR1ASMAD4 | Hereditary mixed polyposis syndrome (HMPS) (OMIM 601228) | AD | Assoc w/ risk for CRC multiple different types of colorectal polyps. Characteristic lesions are mixed juvenile-adenomatous colon polyps. Adenomas, hyperplastic serrated adenomas, mixed hyperplastic-adenomatous polyps may also occur. |
Biomarker and diagnostic research for carcinoma of liver and intrahepatic biliary tract has been reported in the published literature.
No approved treatments are currently available for carcinoma of liver and intrahepatic biliary tract. The disease remains an area of unmet medical need.
Individuals who are diagnosed with classic familial adenomatous polyposis (FAP) or attenuated FAP should be counseled about age-appropriate recommendations for and , in addition to , as outlined in this section. Currently, consensus management guidelines for gastric adenocarcinoma and proximal polyposis of the stomach (GAPPS) are unavailable.
Practice parameters, including information on surgery, have been outlined by the following professional groups:
National Comprehensive Cancer Network (NCCN) (full text)
American Society for Gastrointestinal Endoscopy (full text)
American College of Gastroenterology (full text)
American Society of Colon and Rectal Surgeons (full text)
American Society of Clinical Oncology (full text)
British Society of Gastroenterology (full text)
Society of Surgical Oncology (full text)
(full text)
European Society of Gastrointestinal Endoscopy (full text)
Source: GeneReviews — "APC-Associated Polyposis Conditions"
Surgery and desmoid risk. There is evidence that the risk of developing desmoid tumors is increased following abdominal surgery and may be higher following surgical procedures that require two stages. Individuals at high risk for desmoids (e.g., women, those with APC pathogenic variants in codons 1395-1493, those with a family history of desmoids) should consider an operation that is likely to be a single stage to minimize the need for a second surgery. Surgery and fecundity. There is the likelihood of a lower rate of fecundity in women after a total colectomy with IPAA . Although most of the concern is related to results from surgeries performed for inflammatory bowel disease, this issue should be included as part of the discussion of surgical options with women with FAP .
Source: GeneReviews — "APC-Associated Polyposis Conditions"
In a single controlled trial, the omega-3 polyunsaturated fatty acid eicosapentaenoic acid (EPA) led to a 20%-30% decrease in FAP polyp size and number . A Phase III multicenter trial studying the effect of EPA on rectal polyp burden after total colectomy with IRA is currently under way (NCT03806426). There are also currently several multicenter trials on obeticholic acid, lorpucitinib (pan-janus kinase inhibitor), encapsulated sirolimus, and guselkumab (IL-23 inhibitor). Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions.
Source: GeneReviews — "APC-Associated Polyposis Conditions"
3 trials found
Multiple professional societies have published guidelines based on the available evidence to date as well as expert consensus . The following surveillance recommendations are based on these expert society guidelines. Table 6. Recommended Surveillance for Individuals with FAP
System/Concern | Evaluation | Frequency/Comment |
|---|---|---|
polyps | Colonoscopy | Every 1-2 yrs beginning: at age 10-15 yrs for classic FAP; in late adolescence for attenuated FAP In persons who have undergone subtotal colectomy w/ileorectal anastomosis: surveillance of remaining rectum |
polyps cancer | EGD w/complete visualization of ampulla of Vater (using duodenoscope or clear cap) | Every 6 mos-5 yrs depending on duodenal adenoma burden2 beginning at age 20-25 yrs or prior to colectomy Consider complete small bowel visualization by video capsule endoscopy or CT/MR enterography esp if duodenal polyposis is advanced (based on Spigelman scoring system). |
CNS tumors | Neurologic exam | Annually beginning at diagnosis Hepatoblastoma |
cancer | EGD | Every 6 mos-5 yrs (w/duodenal exam), beginning at age 20-25 yrs; If polyps are neoplastic or large consider annual exams. Non-malignant extraintestinal manifestations |
Source: GeneReviews — "APC-Associated Polyposis Conditions"
3 clinical trials registered, 1 recruiting. Interventions under study include other interventions, drug therapy, medical devices, and procedural interventions. Pipeline includes 1 PHASE2. Research is sponsored by a mix of industry and academic institutions.
150 publications have been identified in PubMed for carcinoma of liver and intrahepatic biliary tract. Research spans Review / Meta-Analysis (35%), Epidemiology / Natural History (19%), and Basic Science / Preclinical (15%).
Research Type | Count | % of Total |
|---|---|---|
Research summaries | 48 | 35% |
Disease patterns and progression | 26 | 19% |
Laboratory research | 21 | 15% |
Patient case studies | 17 | 12% |
Clinical study results | 17 | 12% |
Testing and diagnosis research | 8 | 6% |
Other research | 1 | 1% |
Zorigtbaatar A (2026). [PMID: 41776242](https://pubmed.ncbi.nlm.nih.gov/41776242/). *Nat Rev Clin Oncol*. [Review / Meta-Analysis]
Jang EJ (2026). [PMID: 41566127](https://pubmed.ncbi.nlm.nih.gov/41566127/). *Ann Surg Oncol*. [Case Report / Case Series]
Lin S (2026). [PMID: 42017899](https://pubmed.ncbi.nlm.nih.gov/42017899/). *Cancer Biomark*. [Epidemiology / Natural History]
Pang C (2026). [PMID: 41528222](https://pubmed.ncbi.nlm.nih.gov/41528222/). *Radiology*. [Epidemiology / Natural History]
Lang H (2026). [PMID: 41537967](https://pubmed.ncbi.nlm.nih.gov/41537967/). *Chirurgie (Heidelb)*. [Clinical Trial Publication]
Zheng Q (2026). [PMID: 40967375](https://pubmed.ncbi.nlm.nih.gov/40967375/). *Int J Radiat Oncol Biol Phys*. [Epidemiology / Natural History]
Jansson H (2026). [PMID: 41492113](https://pubmed.ncbi.nlm.nih.gov/41492113/). *Ann Surg Oncol*. [Epidemiology / Natural History]
Itano O (2026). [PMID: 41488837](https://pubmed.ncbi.nlm.nih.gov/41488837/). *Ann Gastroenterol Surg*. [Review / Meta-Analysis]
Choubey AP (2026). [PMID: 41872621](https://pubmed.ncbi.nlm.nih.gov/41872621/). *Ann Surg Oncol*. [Case Report / Case Series]
Nakanuma Y (2026). [PMID: 42122152](https://pubmed.ncbi.nlm.nih.gov/42122152/). *Cancers (Basel)*. [Review / Meta-Analysis]
Data assembled from 5 of 12 sources · Last updated Sep 20, 2026, 4:39 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
AXIN2 | AXIN2-assoc polyposis (oligodontia-CRC syndrome) (OMIM 608615) | AD | Ectodermal dysplasia BMPR1A |
SMAD4 | Juvenile polyposis syndrome (JPS) | AD | Characterized by predisposition for hamartomatous polyps, which is often the distinguishing feature between FAP JPS. Hamartomatous polyps occur in the GI tract – specifically stomach, small intestine, colon, rectum. Most persons w/JPS have some polyps by age 20 yrs. |
PMS2 | Lynch syndrome (hereditary non-polyposis colon cancer) | AD | It may be difficult to distinguish Lynch syndrome from attenuated FAP in persons w/early-onset CRC few adenomatous colonic polyps. Family history of extracolonic cancers manifestations, MSI testing, /or IHC testing on tumor tissue may be helpful in distinguishing the 2 disorders. MLH1 MSH2 MSH6 |
PMS2 | Constitutional mismatch repair deficiency (CMMRD) (See Lynch syndrome.) | AR | Affected persons frequently have brain tumors, hematologic malignancies, CRC, /or other Lynch syndrome cancers in childhood. Caf au lait macules /or axillary/inguinal freckling are seen in most persons; multiple colorectal adenomas mimicking attenuated FAP may also be present. |
MSH3 | MSH3-assoc polyposis (OMIM 617100) | AR | Colorectal duodenal adenomas, CRC, gastric cancer, early-onset astrocytoma |
MUTYH | MUTYH polyposis (MAP) | AR | Assoc w/predisposition to multiple adenomas or polyposis coli. The colonic phenotype of MAP can be similar to attenuated FAP. If an APC pathogenic variant is not identified in a person w/colonic polyposis, molecular genetic testing of MUTYH should be considered. |
NF1 | Neurofibromatosis type 1 (NF1) | AD | Persons w/NF1 may exhibit multiple intestinal polypoid neurofibromas or ganglioneuromas in small bowel, stomach, colon. |
NTHL1 | NTHL1 tumor syndrome (NTHL1-assoc polyposis) | AR | Characterized by lifetime risk for CRC, breast cancer, colorectal polyposis. |
Source: GeneReviews — "APC-Associated Polyposis Conditions"