Kabakus Ismail Mikdat, Atceken Zeynep, Ariyurek Orhan Macit
Department of Radiology, Erzurum Regional Training and Research Hospital, Erzurum, Turkey.
Department of Radiology, Koç University School of Medicine, İstanbul, Turkey.
Eurasian J Med. 2017 Feb;49(1):64-65. doi: 10.5152/eurasianjmed.2017.17004.
Intrathoracic ribs are very rare congenital anomalies. Approximately 50 cases have been reported in the literature till date. They are usually present on the right side, between the third and eighth ribs without sex predominance. They may originate from a vertebral body or the proximal or distal part of a rib. In most cases, they are asymptomatic, but they may be associated with developmental abnormalities of ribs and vertebrae. The diagnosis is important to prevent further investigation or intervention. Here we present two rare cases with supernumerary intrathoracic rib and describe a novel sign, namely expansion of the rib head. To the best of our knowledge, this is the shortest supernumerary intrathoracic rib, reported in the literature, on the left side originating from the head of the second rib, which could have been misdiagnosed as osteochondroma due to its atypical features.
胸内肋骨是非常罕见的先天性异常。迄今为止,文献中报道了约50例。它们通常出现在右侧,位于第三至第八肋骨之间,无性别差异。它们可能起源于椎体或肋骨的近端或远端。在大多数情况下,它们是无症状的,但可能与肋骨和椎骨的发育异常有关。该诊断对于避免进一步的检查或干预很重要。在此,我们报告两例罕见的胸内多余肋骨病例,并描述一种新体征,即肋骨头扩大。据我们所知,这是文献中报道的最短的左侧胸内多余肋骨,起源于第二肋骨头,因其非典型特征可能被误诊为骨软骨瘤。