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S5098 Cronkhite-Canada Syndrome: A Rare Presentation for Weight Loss, Diarrhea and Protein-Losing Enteropathy

2024· article· en· W4403719309 on OpenAlexaboutno aff
Swetha Tummala, Sanjeev Tummala

Bibliographic record

VenueThe American Journal of Gastroenterology · 2024
Typearticle
Languageen
FieldMedicine
TopicGenetic factors in colorectal cancer
Canadian institutionsnot available
Fundersnot available
KeywordsMedicineProtein losing enteropathyEnteropathyDiarrheaPresentation (obstetrics)Weight lossIntestinal malabsorptionPediatricsGastroenterologyDermatologyInternal medicineSurgeryDiseaseCoeliac diseaseObesity

Abstract

fetched live from OpenAlex

Introduction: Cronkhite-Canada syndrome (CCS) is a rare, nonhereditary polyposis syndrome that causes protein-losing enteropathy, weight loss, diarrhea, and skin changes. Around 500 cases have been documented worldwide in 50 years. CCS is difficult to diagnose and many patients fail therapy and have high morbidity and mortality. We report CCS in a 62-year-old Asian man. Case Description/Methods: A 62-year-old healthy man presented with several weeks of bloating, loss of smell and taste, decreased appetite, diarrhea, darkened hands, and fingernail splitting (Figure) following a screening colonoscopy, which showed 3 small benign polyps. He also endorsed 50 pounds of weight loss over 3 months. Extensive investigation of infectious, neoplastic, and inflammatory causes was negative. Stool was positive for occult blood. He developed hypoproteinemia and markedly elevated calprotectin level to 4,260 μg/g. Endoscopy and repeat colonoscopy was performed with endoscopic ultrasound. This showed thickened polypoid folds in the stomach (Figure), duodenum, and colon. Pathology revealed edematous lamina propria and cystically dilated glands throughout the gastrointestinal tract (Figure 1). A diagnosis of CCS was made. The patient was started on prednisone plus mesalamine and a high-calorie, high-protein diet. In 3 months, he gained 20 pounds, and all of his symptoms improved. He continues to be followed by gastroenterology. Discussion: CCS is rare. Most reported cases are from Asia. The etiology is unknown, but an autoimmune etiology has been purported due to positive responses to immunosuppression. Diagnosis combines clinical features of chronic diarrhea, weight loss, malnutrition, and skin changes with multiple hamartomatous polyps in the gastrointestinal tract. Management is primarily immunosuppression with glucocorticoids with or without 5-aminosalicylates. CCS can lead to complications, including infections and blood clots, and increased risk of gastrointestinal cancers. Nutritional support is crucial. Regular upper and lower endoscopies are important to monitor malignant complications. CCS is progressive with a poor prognosis. Given its rarity, prospective data on management is limited, and there are no guidelines for monitoring. This case shows how prompt diagnosis and multifaceted management for this rare syndrome can improve symptoms and disease control and encourages further studies to improve management.Figure 1.: A-Darkened hands and fingernail splitting. B-Image of the stomach obtained during endoscopy shows thickened polypoid folds with edema and inflammation. C-On hematoxylin and eosin staining, the stomach shows polypoid architecture, cystically dilated glands, and edematous lamina propria.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Case report · Consensus signal: Case report
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.010
Threshold uncertainty score0.021

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0020.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0020.001
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0030.001
Insufficient payload (model declined to judge)0.0060.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.251
Teacher spread0.244 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designCase report
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

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Citations0
Published2024
Admission routes1
Has abstractyes

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