Evidence map›Paper›PMID 39546055›Full record

ReviewFamilial cancer2024

Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature.

Maria Laura Gonzalez, Carolina Vazquez, Maria J Argüero, Juan P Santino, Ana Braslavsky, Marcelo M Serra

Abstract readReview
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In one paragraph

Review in Familial cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Maria Laura GonzalezGastroenterology Department, Hospital Italiano de Buenos Aires, J. D. Perón 4190, Ciudad Autónoma de Buenos Aires, C1181ACH, Argentina. marialaura.gonzalez@hospitalitaliano.org.ar.ORCID 0000-0003-0469-7469
Carolina VazquezA.R.G. (Argentine Rendu Study Group), Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0003-2834-9047
Maria J ArgüeroGastroenterology Department, Hospital Italiano de Buenos Aires, J. D. Perón 4190, Ciudad Autónoma de Buenos Aires, C1181ACH, Argentina.ORCID 0000-0002-7947-270X
Juan P SantinoPathology Department, Hospital Italiano de Buenos Aires, J. D. Perón 4190, Ciudad Autónoma de Buenos Aires, C1181ACH, Argentina.ORCID 0000-0001-9927-4965
Ana BraslavskyA.R.G. (Argentine Rendu Study Group), Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0001-8169-171X
Marcelo M SerraA.R.G. (Argentine Rendu Study Group), Ciudad Autónoma de Buenos Aires, Argentina.ORCID 0000-0002-9912-9503

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary Hemorrhagic Telangiectasia (HHT) is an autosomal vascular dysplasia characterized by the presence of mucocutaneous telangiectasia and arteriovenous malformations in solid organs. The Curaçao criteria and/or detection of ALK1, ENG, and SMAD4 gene mutations are used for diagnosis. Juvenile Polyposis Syndrome (JPS) is diagnosed according to the number and localization of juvenile polyps, and family history of JPS. Both entities have a low prevalence. Mutation of SMAD4 leads to a combined syndrome of these two conditions called HHT-JPS Overlap Syndrome. We aim to describe the clinical characteristics associated with this condition focusing on long term follow up and review of the literature. A cross-sectional descriptive study of HHT-JPS cases from an HHT Institutional Registry was designed. Patients were eligible for this case series if they fulfilled both HHT and JPS diagnostic criteria and/or mutation on SMAD4. A comprehensive review was conducted on the clinical phenotype associated with HHT and its gastrointestinal involvement. Fourteen patients from eleven families in 788 previously HHT-diagnosed patients met the inclusion criteria. The ages ranged between 25 and 70 years old and 12 were females. In addition to the typical signs/symptoms of HHT, two distinct phenotypes were observed. Nine patients predominantly exhibited initially upper, while five showed predominantly initially lower gastrointestinal involvement. Numerous musculoskeletal and cardiovascular anomalies were also identified. The observed phenotypic diversity, particularly in gastrointestinal involvement, underscores the need for tailored clinical approaches. Comprehensive assessments identified associated musculoskeletal and cardiovascular anomalies, emphasizing the systemic nature of HHT-JPS.

Indexed as

Intestinal PolyposisNeoplastic Syndromes, HereditarySmad4 ProteinTelangiectasia, Hereditary HemorrhagicAdultAgedCross-Sectional StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedMutationPhenotypeSmad4 ProteinSMAD4 protein, humanColectomyDigestive cancerGastrectomyGastrointestinal cancerOsler weber renduPolypsSMAD4 mutation

Identifiers

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.