Sternal cleft and pectus excavatum: an overlooked congenital association?
Pediatr Surg Int
; 40(1): 105, 2024 Apr 11.
Article
em En
| MEDLINE
| ID: mdl-38602580
ABSTRACT
BACKGROUND:
Sternal cleft (SC), a rare thoracic malformation, is associated with pectus excavatum (PE) in 2.6-5% of cases. It remains unclear if these conditions are congenitally linked or if SC repair triggers PE. To investigate the potential higher frequency of PE in SC cases, we conducted a retrospective study of our SC patients.METHODS:
We assessed PE incidence, progression, and management in SC patients treated at our institute from 2006 to 2022. When available, we collected pre-SC repair CT scan data, calculating the Haller Index (HI) and Correction Index (CI) and compared them to a selected control group.RESULTS:
Among 8 SC patients, 7 had concomitant PE (87.5%), varying in severity. PE management ranged from observation to thoracoplasty, depending on its degree. We observed a significant pre-operative CI difference between SC and control group patients (p < 0.00001). In the last two SC repair cases, we attempted concurrent PE prevention or treatment.CONCLUSION:
Our findings suggest an underestimated association between PE and SC in the existing literature. SC patients may exhibit a predisposition to PE from birth, which may become more apparent with growth after SC repair. Consequently, PE prevention or treatment should be considered during SC repair procedures.Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Esterno
/
Tórax em Funil
/
Anormalidades Musculoesqueléticas
Limite:
Humans
Idioma:
En
Revista:
Pediatr Surg Int
Ano de publicação:
2024
Tipo de documento:
Article