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Overlap syndrome of hereditary hemorrhagic telangiectasia and juvenile polyposis syndrome: ten years follow-up-case series and review of literature.
- Source :
-
Familial cancer [Fam Cancer] 2024 Nov 15; Vol. 24 (1), pp. 1. Date of Electronic Publication: 2024 Nov 15. - Publication Year :
- 2024
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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.<br />Competing Interests: Declarations Competing interests The authors declare no competing interests.<br /> (© 2024. The Author(s), under exclusive licence to Springer Nature B.V.)
- Subjects :
- Humans
Female
Adult
Male
Middle Aged
Follow-Up Studies
Aged
Cross-Sectional Studies
Mutation
Phenotype
Telangiectasia, Hereditary Hemorrhagic genetics
Telangiectasia, Hereditary Hemorrhagic complications
Smad4 Protein genetics
Neoplastic Syndromes, Hereditary genetics
Intestinal Polyposis genetics
Intestinal Polyposis congenital
Intestinal Polyposis complications
Subjects
Details
- Language :
- English
- ISSN :
- 1573-7292
- Volume :
- 24
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Familial cancer
- Publication Type :
- Academic Journal
- Accession number :
- 39546055
- Full Text :
- https://doi.org/10.1007/s10689-024-00425-9