Cronkhite-Canada syndrome — acquired non-Mendelian polyposis- ectodermal syndrome. Rare (...
Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.
| ID | RF-CRONKHITE-CANADA-CONFIRMED |
|---|---|
| Type | Red flag |
| Status | reviewed 2026-05-20 | pending_clinical_signoff |
| Diseases | DIS-CRC DIS-GASTRIC |
| Sources | SRC-AGA-IBD-CRC-2024 SRC-NCCN-GENETIC-FAMILIAL-CRC-2025 |
Red Flag Origin
| Definition | Cronkhite-Canada syndrome — acquired non-Mendelian polyposis- ectodermal syndrome. Rare (~1000 reported cases globally; primarily middle-aged + elderly adults). Clinical presentation: gastrointestinal polyposis (juvenile-like, throughout stomach + small bowel + colon diffusely) + ectodermal changes (diffuse alopecia, nail dystrophy with onycholysis, skin hyperpigmentation) + protein-losing enteropathy (hypoalbuminemia, edema, weight loss, electrolyte derangement). Lifetime CRC risk ~12-25%; gastric cancer also elevated per IPCG case-series. Pathogenesis unclear — autoimmune-like; may respond to immunosuppression (prednisone, azathioprine) + nutritional support; untreated mortality high (~50% 5-year if uncontrolled). Diagnosis is clinical + supported by classic GI biopsy + ectodermal pattern. Patient has confirmed clinical diagnosis; no current personal cancer diagnosis. Prevention-perso... |
|---|---|
| Clinical direction | investigate |
| Category | other |
Trigger Logic
{
"any_of": [
{
"finding": "cronkhite_canada_clinical_diagnostic_criteria_met",
"value": true
},
{
"finding": "gastrointestinal_polyposis_with_ectodermal_changes",
"value": true
},
{
"finding": "protein_losing_enteropathy_with_diffuse_gi_polyposis",
"value": true
}
],
"type": "lab_value"
}
Notes
Prevention-persona RedFlag for Cronkhite-Canada syndrome. risk_category set to chronic_condition (not genetic) because etiology is acquired autoimmune-like + non-Mendelian. Surveillance: colonoscopy q1-2y from diagnosis; upper endoscopy q1-2y; small-bowel capsule q2y; treat active disease with immunosuppression (prednisone taper + azathioprine maintenance) + nutritional support (protein replacement, electrolyte correction). Mortality reduced markedly with immuno- suppression treatment. STUB pending two-Co-Lead signoff per CHARTER §6.1 dev-mode.
Used By
Indications
IND-CRONKHITE-CANADA-OBSERVATION- IND-CRONKHITE-CANADA-OBSERVATIONIND-CRONKHITE-CANADA-SURVEILLANCE- IND-CRONKHITE-CANADA-SURVEILLANCE