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A systematic review of Bannayan - Riley - Ruvalcaba syndrome.
Kapacinskaite, Medeine; Stratica, Natalia; Adomaitiene, Irina; Rascon, Jelena; Vaisnyte, Birute.
Afiliación
  • Kapacinskaite M; Faculty of Medicine, Vilnius University, M.K. Ciurlionio g. 21, 03101, Vilnius, Lithuania. medeine.kapac@gmail.com.
  • Stratica N; University of Medicine and Pharmacy "Grigore T. Popa", Strada Universitații 16, 700115, Iași, Romania.
  • Adomaitiene I; Center for Pediatric Oncology and Hematology, Vilnius University Hospital Santaros Klinikos, Santariskiu 24, 08406, Vilnius, Lithuania.
  • Rascon J; Clinic of Pediatrics, Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania.
  • Vaisnyte B; Faculty of Medicine, Vilnius University, M.K. Ciurlionio g. 21, 03101, Vilnius, Lithuania.
Sci Rep ; 14(1): 21119, 2024 09 10.
Article en En | MEDLINE | ID: mdl-39256443
ABSTRACT
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare overgrowth condition caused by a pathogenic variant in the phosphatase and tensin homolog (PTEN) gene and belongs to a group of disorders called PTEN hamartoma tumor syndrome (PHTS). The diagnosis is often complicated by great phenotypic diversity. Furthermore, to this date treatment options are limited. Here we performed a systematic review using PubMed, Cochrane, and Scopus databases to identify cases of pediatric patients diagnosed with BRRS and summarized information about the clinical presentation, treatment, and long-term patient care. A total of 83 pediatric patients with BRRS were identified. The most common clinical findings were macrocephaly (77%) and developmental disorders (63%). Surgical interventions were the treatment of choice, described in 19 articles. Patient surveillance was proposed in 15 case reports and mostly aimed at periodic cancer screening. Recognition of BRRS clinical symptoms and early referral to a geneticist is important for better disease control and overall prognosis. As targeted treatment is still lacking, symptom relief and long-term surveillance remain the main management strategies.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Fosfohidrolasa PTEN Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Lituania Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Hamartoma Múltiple / Fosfohidrolasa PTEN Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Lituania Pais de publicación: Reino Unido