Abdollahifar Mohammad-Amin, Abdi Shabnam, Bayat Mohammad, Masteri Farahani Reza, Abbaszadeh Hojjat-Allah
Department of Anatomical Sciences and Biology, Shahid Beheshti University of Medical Science, Tehran, Iran.
Department of Anatomical Science, Tehran Medical Sciences Branch, Islamic Azad University, Tehran, Iran.
Anat Cell Biol. 2017 Mar;50(1):73-75. doi: 10.5115/acb.2017.50.1.73. Epub 2017 Mar 29.
One of the uncommon congenital variations is intrathoracic rib which a normal, a bifid, or an accessory rib lies within the thoracic cavity that is founded accidentally. Clinically, in most cases they are without symptoms; however, it may cause intrathoracic problems therefore it is important for radiologists and physicians to identify to prevent of excessive intervention and treatment during imaging diagnostic techniques of thoracic problems. In this report, we provide the case of a rare presentation of an intrathoracic rib in a 3-year-old boy arising from the inferior portion of a second rib based on findings from computed tomography. To our knowledge, this is only the second reported case of this type of intrathoracic rib that demonstrated with computed tomography.
一种罕见的先天性变异是胸腔内肋骨,即正常、分叉或副肋骨位于胸腔内,多为偶然发现。临床上,大多数情况下它们没有症状;然而,它可能会引起胸腔内问题,因此放射科医生和医生识别它很重要,以防止在胸部问题的影像诊断技术过程中过度干预和治疗。在本报告中,我们根据计算机断层扫描的结果,提供了一名3岁男孩罕见的胸腔内肋骨病例,该肋骨起源于第二肋骨的下部。据我们所知,这是第二例通过计算机断层扫描显示的此类胸腔内肋骨病例。