Congenital rib absence with liver herniation: A case report

Yirgalem Teklebirhan Gebreziher , Feven Mekonen Tadesse , Hadush Tesfay Negash , Berihu Tadish Gebre
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Abstract

Introduction

Congenital rib absence with liver herniation is an extremely rare condition. Only a few cases have been reported, and most of them have been associated with Poland syndrome.

Case presentation

A full-term female newborn, born at 38 weeks of gestation with a birth weight of 3100 g, delivered vaginally following a normal pregnancy was brought to our clinic at 11 days of life for a right lower thoracic bulge. There was no relevant family history. The physical exam was completely normal except for a 4 × 5 cm round protrusion in the right lower anterolateral chest. The ribs in the area were clearly absent. The skin, the subcutaneous tissue and the muscles appeared normal. He had normal vital signs and breath sounds. The abdominal exam was normal. A plain chest X-ray showed normal lung fields, absence of the right lower ribs, a right diaphragmatic eventration, and a soft tissue herniation. A three-dimensional computed tomography (3D-CT) reconstruction confirmed the diagnosis of congenital hypoplastic 6th and 7th right ribs, absent 8th and 9th right ribs, and a foramen in the right 10th rib. It also showed that the visible bulge was the liver protruding through the weakened chest wall. The only other anatomical anomaly was 6th to 9th thoracic butterfly vertebrae. The patient is being managed conservatively and is doing well.

Conclusion

Congenital intercostal liver herniation with absent ribs is an extremely rare condition and can be managed conservatively in asymptomatic cases. We recommend 3D-CT reconstruction as an effective way to confirm the diagnosis and rule out associated malformations.
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先天性肋骨缺失伴肝疝:病例报告
导言先天性肋骨缺失伴肝疝是一种极为罕见的疾病。病例介绍 一名足月女婴,妊娠 38 周,出生体重 3100 克,正常妊娠后经阴道分娩,出生 11 天时因右胸下段隆起被送至我院就诊。没有相关的家族病史。体格检查完全正常,只是右胸前下侧有一个 4 × 5 厘米的圆形突起。该区域的肋骨明显缺失。皮肤、皮下组织和肌肉均正常。生命体征和呼吸音正常。腹部检查正常。胸部 X 光片显示肺野正常,右下侧肋骨缺失,右侧膈肌分离,软组织疝。三维计算机断层扫描(3D-CT)重建确诊为先天性右第 6 和第 7 肋骨发育不良,右第 8 和第 9 肋骨缺失,右第 10 肋骨有一个孔。它还显示,可见的隆起是肝脏穿过薄弱的胸壁突出。唯一的其他解剖异常是第 6 至第 9 胸椎。结论先天性肋间肝疝伴肋骨缺失是一种极为罕见的疾病,对于无症状的病例可以采取保守治疗。我们建议将三维 CT 重建作为确诊和排除相关畸形的有效方法。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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