Choi Paul J, Iwanaga Joe, Tubbs R Shane
Clinical Anatomy, Seattle Science Foundation.
Seattle Science Foundation.
Cureus. 2017 Dec 8;9(12):e1929. doi: 10.7759/cureus.1929.
A sternal foramen (SF), which arises from the incomplete fusion of the cartilaginous neonatal sternum, is a relatively common anatomical variation found in 2.5% to 13.8 % of all individuals. SFs are usually located at the lower third of the sternal body and their average diameter is 6.5 mm. An SF is subclinical; however, its close proximity to the thoracic organs, i.e., the heart and lungs, entails a risk of serious complications from blinded sternal interventions. Moreover, its presence can lead to misinterpretation of radiological and postmortem findings. The SF is ignored by many physicians and non-physician healthcare providers who must understand its clinical significance in order to optimize patient care. Our aim in this review is to highlight the potential clinical consequences for SF patients, discuss recommendations for performing sternal procedures safely when this anatomical variation is present, and preclude radiological and pathological misinterpretations so that patient care can be improved.
胸骨孔(SF)源于新生儿软骨胸骨的不完全融合,是一种相对常见的解剖变异,在所有个体中的发生率为2.5%至13.8%。胸骨孔通常位于胸骨体的下三分之一处,其平均直径为6.5毫米。胸骨孔是亚临床的;然而,它与胸部器官(即心脏和肺)距离很近,这意味着盲目进行胸骨干预会有严重并发症的风险。此外,它的存在可能导致对影像学和尸检结果的误解。许多医生和非医生医疗服务提供者都忽略了胸骨孔,而他们必须了解其临床意义才能优化患者护理。本综述的目的是强调胸骨孔患者潜在的临床后果,讨论存在这种解剖变异时安全进行胸骨手术的建议,并避免影像学和病理学的误解,从而改善患者护理。