Familial Adenomatous Polyposis P022
Current RMA Instruments
| Reasonable Hypothesis SOP | 77 of 2021 |
| Balance of Probabilities SOP | 78 of 2021 |
Changes from previous Instruments
ICD Coding
- ICD-9-CM Codes: 211.31
- ICD-10-AM Codes: D12.6
Brief description
Familial adenomatous polyposis is an inherited autosomal dominant syndrome, characterised by the formation of numerous (typically > 100) colorectal adenomas.
Confirming the diagnosisIs
This diagnosis is based on the finding of a very large number of adenomatous polyps on colonoscopy or sigmoidoscopy, plus a positive gene study.
The relevant medical specialist is a gastroenterologist or colorectal surgeon.
Additional diagnoses covered by SOP
- Familial polyposis coli
- Gardner syndrome
Conditions not covered by SOP
- Malignant neoplasm of the colorectum*
- Benign neoplasms of the colon or rectum - may be covered by the colorectal adenoma SOP or may be non-SOP
- Neoplasms including polyps of the anal canal - non SOP
* another SOP applies
Clinical onset
The condition may be detected by screeening (genetic & colonoscopic) at an early age, based on a positive family history. In others the condition may become clinically apparent, with development of gastrointestinal symptoms (bleeding, diarrhoea, abdominal pain, obstructive symptoms). These symptoms may be from the polyps, or due to the development of colorectal cancer (for which there is a very, very high risk if the polyposis is untreated). In such cases diagnosis is usually between ages 20 and 40. There may be manifestations outside the colorectum that can also point to the diagnosis (e.g. polyps and other benign tumours at other sites).
Clinical worsening
The only SOP factor is for inability to obtain appropriate clinical management. Management comprises either annual screening colonoscopy with polyp excisions, or a colectomy (removal of colon), because of the inevitability of colorectal cancer and the unmanageably high number of polyps. Elective colectomy is typically performed in the late teens or early 20s.
Source URL: https://clik.dva.gov.au/ccps-medical-research-library/sops-grouped-icd-body-system/e-g/familial-adenomatous-polyposis-p022-d126
Rulebase for familial adenomatous polyposis
<h5><strong>Current RMA Instruments</strong></h5><table border="1" cellspacing="1" cellpadding="1"><tbody><tr><td><a href="http://www.rma.gov.au/assets/SOP/2021/bf84ed1581/077.pdf" target="_blank"><em><u>Reasonable Hypothesis SOP</u></em></a></td><td><span>77 of 2021</span></td></tr><tr><td><a href="http://www.rma.gov.au/assets/SOP/2021/12966f5bc3/078.pdf" target="_blank"><em><u>Balance of Probabilities SOP </u></em></a></td><td><span>78 of 2021</span></td></tr></tbody></table><h5>Changes from previous Instruments</h5><p><drupal-media data-entity-type="media" data-entity-uuid="876402fd-7f5d-4a67-8784-01380ed70d76" data-view-mode="wysiwyg"></drupal-media></p><h5>ICD Coding</h5><ul><li>ICD-9-CM Codes: 211.31</li><li>ICD-10-AM Codes: D12.6</li></ul><h5><strong>Brief description</strong></h5><p>Familial adenomatous polyposis is an inherited autosomal dominant syndrome, characterised by the formation of numerous (typically > 100) colorectal adenomas.</p><h5><strong>Confirming the diagnosisIs</strong></h5><p>This diagnosis is based on the finding of a very large number of adenomatous polyps on colonoscopy or sigmoidoscopy, plus a positive gene study.</p><p>The relevant medical specialist is a gastroenterologist or colorectal surgeon.</p><h5><strong>Additional diagnoses covered by SOP</strong></h5><ul><li>Familial polyposis coli</li><li>Gardner syndrome</li></ul><h5><strong>Conditions not covered by SOP</strong></h5><ul><li>Malignant neoplasm of the colorectum*</li><li>Benign neoplasms of the colon or rectum - may be covered by the colorectal adenoma SOP or may be non-SOP</li><li>Neoplasms including polyps of the anal canal - non SOP</li></ul><p>* another SOP applies</p><h5>Clinical onset</h5><p>The condition may be detected by screeening (genetic & colonoscopic) at an early age, based on a positive family history. In others the condition may become clinically apparent, with development of gastrointestinal symptoms (bleeding, diarrhoea, abdominal pain, obstructive symptoms). These symptoms may be from the polyps, or due to the development of colorectal cancer (for which there is a very, very high risk if the polyposis is untreated). In such cases diagnosis is usually between ages 20 and 40. There may be manifestations outside the colorectum that can also point to the diagnosis (e.g. polyps and other benign tumours at other sites).</p><h5>Clinical worsening</h5><p>The only SOP factor is for inability to obtain appropriate clinical management. Management comprises either annual screening colonoscopy with polyp excisions, or a colectomy (removal of colon), because of the inevitability of colorectal cancer and the unmanageably high number of polyps. Elective colectomy is typically performed in the late teens or early 20s.</p><p> </p>
Source URL: https://clik.dva.gov.au/ccps-medical-research-library/statements-principles/e-g/familial-adenomatous-polyposis-p022-d126/rulebase-familial-adenomatous-polyposis
No appropriate clinical management for familial adenomatous polyposis
Current RMA Instruments
| Reasonable Hypothesis SOP | 77 of 2021 |
| Balance of Probabilities SOP | 78 of 2021 |
Changes from previous Instruments
ICD Coding
- ICD-9-CM Codes: 211.31
- ICD-10-AM Codes: D12.6
Brief description
Familial adenomatous polyposis is an inherited autosomal dominant syndrome, characterised by the formation of numerous (typically > 100) colorectal adenomas.
Confirming the diagnosisIs
This diagnosis is based on the finding of a very large number of adenomatous polyps on colonoscopy or sigmoidoscopy, plus a positive gene study.
The relevant medical specialist is a gastroenterologist or colorectal surgeon.
Additional diagnoses covered by SOP
- Familial polyposis coli
- Gardner syndrome
Conditions not covered by SOP
- Malignant neoplasm of the colorectum*
- Benign neoplasms of the colon or rectum - may be covered by the colorectal adenoma SOP or may be non-SOP
- Neoplasms including polyps of the anal canal - non SOP
* another SOP applies
Clinical onset
The condition may be detected by screeening (genetic & colonoscopic) at an early age, based on a positive family history. In others the condition may become clinically apparent, with development of gastrointestinal symptoms (bleeding, diarrhoea, abdominal pain, obstructive symptoms). These symptoms may be from the polyps, or due to the development of colorectal cancer (for which there is a very, very high risk if the polyposis is untreated). In such cases diagnosis is usually between ages 20 and 40. There may be manifestations outside the colorectum that can also point to the diagnosis (e.g. polyps and other benign tumours at other sites).
Clinical worsening
The only SOP factor is for inability to obtain appropriate clinical management. Management comprises either annual screening colonoscopy with polyp excisions, or a colectomy (removal of colon), because of the inevitability of colorectal cancer and the unmanageably high number of polyps. Elective colectomy is typically performed in the late teens or early 20s.
Source URL: https://clik.dva.gov.au/ccps-medical-research-library/statements-principles/e-g/familial-adenomatous-polyposis-p022-d126/rulebase-familial-adenomatous-polyposis/no-appropriate-clinical-management-familial-adenomatous-polyposis