Two rare cases of the Pentalogy of Cantrell or its variants.

Acta medica Austriaca Pub Date : 2004-08-01
Adnan Aslan, Güngör Karagüzel, Ilke Unal, Nazif Aksoy, Mustafa Melikoglu
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Abstract

The Pentalogy of Cantrell (PC) is a rare association of defects involving the lower sternum, abdominal wall, diaphragm, pericardium and heart. We report two rare cases of the PC (variant form), showing fatal progression. Case 1 only survived two hours because of severe cardio-respiratory failure. Physical examination showed midline abdominal and thoracic defects, ectopic heart, pericardial defect, diaphragmatic defect, bilateral undescended testis, scoliosis, and adherence between left upper limb and trunk. In addition, the autopsy revealed diaphragmatic agenesia, intraabdominal testis, bilateral lung hypoplasia and lymphocytic meningitis. Case 2 only survived 15 minutes. In addition to the physical findings, including lower sternal defect, ectopic heart, epigastric omphalocele and scoliosis, the autopsy showed left diaphragmatic agenesia, pericardial agenesia, bilateral lung hypoplasia, deformed rib cage, anterior thoracic myeloschisis, adreno-hepatic fusion, left renal agenesia, meckel diverticulum and multiple accessory spleens. When comparing with other cases of PC, the concurrence of bilateral intraabdominal testis and lymphocytic meningitis in case 1, and adreno-hepatic fusion, anterior myeloschisis, meckel diverticulum, multiple accessory spleens, and renal agenesia in case 2 have not been described previously.

两例罕见的坎特雷尔五联症或其变种。
Cantrell五联症(PC)是一种罕见的胸骨下、腹壁、横膈膜、心包和心脏的病变。我们报告两例罕见的PC(变体形式),显示致命的进展。病例1因为严重的心肺衰竭只存活了两个小时。体格检查显示腹部和胸部中线缺损,异位心脏,心包缺损,膈缺损,双侧睾丸隐睾,脊柱侧凸,左上肢与躯干粘连。此外,尸检显示膈肌萎缩,腹内睾丸,双侧肺发育不全和淋巴细胞性脑膜炎。病例2只存活了15分钟。尸检除胸骨下段缺损、心异位、腹上脐膨出、脊柱侧凸等物理表现外,还表现为左膈肌萎缩、心包萎缩、双侧肺发育不全、胸腔畸形、胸前段髓裂、肾上腺肝融合、左肾萎缩、梅克尔憩室及多发副脾。与其他PC病例相比,病例1并发双侧腹内睾丸和淋巴细胞性脑膜炎,病例2并发肾上腺肝融合、前髓裂、梅克尔憩室、多发副脾和肾功能不全,均未见文献报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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