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Record W2921769246 · doi:10.1093/jcag/gwz006.147

A148 SIROLIMUS FOR PRIMARY INTESTINAL LYMPHANGIECTASIA IN A PEDIATRIC PATIENT

2019· article· en· W2921769246 on OpenAlexaff
Jaclyn Strauss, Dominica Gidrewicz, L McKenzie

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2019
Typearticle
Languageen
FieldMedicine
TopicVascular Malformations and Hemangiomas
Canadian institutionsAlberta Children's HospitalUniversity of Calgary
Fundersnot available
KeywordsHypoalbuminemiaProtein losing enteropathyMedicineInternal medicineGastroenterologyLymphangiectasiaEnteropathyPathologyEndocrinologyLymphatic system

Abstract

fetched live from OpenAlex

Primary intestinal lymphangiectasia (PIL) is a rare digestive disorder characterized by morphologic abnormalities in the intestinal lymphatics resulting in protein losing enteropathy (PLE). PIL usually presents early in childhood with persistent diarrhea, peripheral edema and ascites. Diet is the cornerstone of medical management, along with iv albumin infusions. Octreotide has been used in more severe cases. Altered expression of lymphangiogenesis regulator genes has been demonstrated in PIL. Several reports have suggested that blocking expression of vascular endothelial growth factor (VEGF), a key regulator in lymphangiogenesis, via the mTOR signaling pathway, may have some clinical benefit in PIL. To describe a unique presentation of primary intestinal lymphangiectasia and share our experiences in clinical management, including a novel treatment with sirolimus. Case report and literature review. We present the case of a 12-year-old boy who initially presented at 8 years of age with tetany and hypocalcemia, along with a 4-month history of intermittent abdominal pain, fatigue and weight loss. Initial investigations revealed severe hypovitaminosis D, hypoalbuminemia, hypoglobulinemia and elevated fecal alpha-1-antitrypsin. Upper endoscopy revealed antral nodularity and ulceration and was positive for H.pylori. He was diagnosed with PLE secondary to H.pylori infection and pseudohypoparathyroidism. Due to persistent hypoalbuminemia and lymphopenia after triple therapy, repeat endoscopy was performed. Biopsies showed intestinal lymphangiectasia in the duodenum and video capsule endoscopy revealed jejunal involvement as well and he was diagnosed with PIL. He responded to a high protein, low fat diet with high medium-chain triglyceride (MCT) content and albumin infusions; serum albumin was 32 g/L at maximal response. Octreotide was later initiated due to increasing edema and fatigue, which resulted in clinical and biochemical improvement along with decreased dependence on albumin infusions. Unfortunately, his response waned over time and he presented 4 years later with severe fatigue, edema, frequent stooling, hypoalbuminemia and lymphopenia. Based on reports that mTOR inhibitors may be a promising treatment for PIL, we initiated treatment with sirolimus in July 2018. Despite no significant improvement in albumin levels as of yet, the patient has demonstrated improved energy and his albumin has remained stable despite no intercurrent albumin infusions. We are continuing to optimize dosing and monitor for clinical response to this novel treatment. To the best of our knowledge, this is the first reported case using sirolimus for treatment of PIL refractory to standard medical management. The patient’s prognosis and clinical course remain to be determined. None

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.027
Threshold uncertainty score0.991

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

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 head0.005
GPT teacher head0.207
Teacher spread0.202 · 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 teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
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".

Quick stats

Citations4
Published2019
Admission routes1
Has abstractyes

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