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Record W2972784740 · doi:10.5489/cuaj.6254

Canadian Urological Association Best Practice Report on the long-term followup for patients with pheochromocytomas

2019· article· en· W2972784740 on OpenAlexaffvenueabout
Ravi Kumar, Philippe D. Violette, Christopher Tran, Eva Tomiak, Jason Izard, Varun Bathini, Neal Rowe

Bibliographic record

VenueCanadian Urological Association Journal · 2019
Typearticle
Languageen
FieldMedicine
TopicAdrenal and Paraganglionic Tumors
Canadian institutionsUniversity of SaskatchewanKingston Health Sciences CentreQueen's UniversityMcMaster UniversityChildren's Hospital of Eastern OntarioImpactOttawa HospitalHamilton Health SciencesUniversity of Ottawa
Fundersnot available
KeywordsPheochromocytomaMedicineMetanephrinesAsymptomaticMalignancyNormetanephrineAdrenalectomyDiseaseMetanephrineIncidentalomaRadiologyInternal medicine

Abstract

fetched live from OpenAlex

Background Pheochromocytoma is a tumor of the catecholamine-producing cells of the adrenal medulla. The incidence is estimated to be 1–2 cases per 100 000 individuals and they make up approximately 5% of incidental adrenal masses.1 Classical symptoms of pheochromocytomas include headache, episodic perspiration, tachycardia, flushing, nausea, and hypertension, although many tumors can be asymptomatic.1 These tumors can be sporadic or hereditary. 2 Familial cases account for up to 30% of tumors.3 Pheochromocytomas can also occur outside the adrenal gland, known as paragangliomas, in up to 25% of cases.4 About 10% of pheochromocytomas are malignant.5 Although there are several clinical and genetic factors associated with an increased risk of malignancy, at this time, there are no molecular, cellular, or histological criteria that can reliably differentiate benign from malignant disease.5 Therefore, malignancy is defined by the presence of clinical metastases. The most common sites for metastases are lymph nodes, bones, liver, and lungs.6 Evaluation of suspected pheochromocytoma begins with confirming a biochemical disturbance by measuring plasma-free metanephrines or urinary fractionated metanephrines, followed by computed tomography (CT) imaging. Once a pheochromocytoma is confirmed, complete surgical resection of the tumor is advised, preferably via laparoscopic or robot-assisted adrenalectomy. The full details regarding workup and treatment of pheochromocytomas is beyond the scope of this review, but there are recent published guidelines on this topic.7 Following surgery, patients are at risk for tumor persistence and recurrence. Despite an overall good prognosis, the disease can recur in up to 16% of patients within 10 years following surgery.8,9 Recurrences may be local or metastatic and have been reported up to 53 years post-initial resection, making long-term followup essential.10 Extra-adrenal disease, hereditary pheochromocytomas, right-sided tumors, bilateral tumors, and larger tumors are thought to be risk factors for recurrence. Currently, there is no consensus on the proper methodology for followup. There have been no randomized studies addressing optimal followup nor prospective registries to provide higher-quality evidence for this issue. Important clinical questions remain regarding duration of followup and which tests should be used to detect and monitor recurrences.

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)0.002
metaresearch head score (Gemma)0.006
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.070
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0020.006
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0010.000

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 head0.010
GPT teacher head0.240
Teacher spread0.230 · 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.

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

Citations8
Published2019
Admission routes3
Has abstractyes

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