Incidental Finding of Dextrocardia with Situs Inversus in a 59-Year-Old Man.

Case Reports in Radiology Pub Date : 2019-12-01 eCollection Date: 2019-01-01 DOI:10.1155/2019/7107293
Emmanuel Kobina Mesi Edzie, Klenam Dzefi-Tettey, Obed Cudjoe, Philip Narteh Gorleku, Patrick Adu
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引用次数: 5

Abstract

Dextrocardia with situs inversus is a rare congenital anomaly, which is characterized by right-sided heart apex and inversely rotated visceral organs of the abdomen. We report an unusual case of dextrocardia with situs inversus in a 59-year-old man, referred for a pelvic ultrasound scan because of symptoms of lower urinary tract obstruction and after a fairly normal prostate specific antigen (PSA) value. A diagnosis of enlarged prostate gland with a prominent median lobe and significant residual urine volume was made, which necessitated the examination of the kidneys for hydronephrosis, resulting in the incidental finding of situs inversus. On further investigation, the diagnosis of dextrocardia with situs inversus was made. Physicians should look out for this anomaly primarily because it may be associated with other conditions like primary ciliary dyskinesia so appropriate interventions are offered to reduce morbidities and mortality.

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一个59岁男性偶然发现右位心性倒置。
右心逆位是一种罕见的先天性畸形,其特征是心尖位于右侧,腹部内脏器官反向旋转。我们报告一个不寻常的病例右心与位置反转在一个59岁的男子,转介盆腔超声扫描,因为下尿路阻塞的症状和相当正常的前列腺特异性抗原(PSA)值。诊断为前列腺肿大,中叶突出,尿量明显残留,需要检查肾脏是否有肾积水,导致偶然发现倒位。经进一步调查,诊断为右心逆位。医生应该注意这种异常,主要是因为它可能与其他疾病有关,如原发性纤毛运动障碍,因此提供适当的干预措施以降低发病率和死亡率。
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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