Miftari Rame, Bicaj Xhavit, Nura Adem, Gerqari Antigona, Fejza Ferki, Bajrami Ismet
Univrsity Clinical Center of Kosova, Deparment of Nuclear Medicine, Prishtina, Kosovo.
Med Arh. 2011;65(6):365-7. doi: 10.5455/medarh.2011.65.365-367.
Renal agenesis is a fairly common congenital anomaly with an unknown definite etiology. Unilateral renal agenesis is much more common than bilateral renal agenesis, but it usually does not carry any major health consequence, as long as the other kidney is healthy. In some cases, renal agenesis may by associated with other congenital anomalies. We report a neonatal female patient born with unilateral renal agenesis associated with malrotation of ipsilateral kidney, anal atresia and pulmonary artery failure.
One month old female child was referred to Nuclear Medicine Department for dynamic renal scintigraphy which performed after intravenously injection of 0.5 mCi(99m) TcDTPA. Scintigraphy was carried out on a Dual Head-Siemens gamma camera using a high resolution collimator. During the dynamic scintigraphy patient was positioned in a supine position. Furosemide, as diuretic stimulator was administered intravenously at 18th minute of the study.
The female patient, eight months old, with cough, short breath (dispnea), fatigue, nausea, vomiting and diarrhea was referred to DTPA renal scintigraphy. Symptoms were manifested ten days before patient had undergone the renal scintigraphy. During this time the patient was under pediatrics' control. A patient has undergone the biochemistry, ultrasound and radiologic examinations. Samples were isolated from the urine culture Pseudomonas aureginosa. The patient received antibiotics (Amikacin) for seven days, whereas last five days she received salbutamole and bisolvon. During physical examination we noticed a left abdominal stoma without palpation sensibility associated with an imperforate anus. From DTPA renal scintigraphy we found the absence of a right kidney, malrotation of a left kidney associated with seriously problems during the elimination of urine.
Unilateral renal agenesis usually is without any major health consequences, but in cases where it is associated with other congenital malformations, such as malrotation of existing kidney, anal atresia and cardiopulmonary anomalies can be very serious problem for life.
Dynamic renal scintigraphy is very highly sensitive and helpful method for detection of renal congenital malformations and function abnormalities.
肾缺如是一种较为常见的先天性异常,确切病因不明。单侧肾缺如比双侧肾缺如更为常见,但只要对侧肾脏健康,通常不会产生任何重大健康问题。在某些情况下,肾缺如可能与其他先天性异常相关。我们报告一例新生儿女性患者,出生时患有单侧肾缺如,并伴有同侧肾脏旋转不良、肛门闭锁和肺动脉发育不全。
一名1个月大的女童被转诊至核医学科进行动态肾闪烁显像,在静脉注射0.5毫居里(99m)锝-二乙三胺五醋酸(TcDTPA)后进行该检查。使用双头西门子γ相机和高分辨率准直器进行闪烁显像。在动态闪烁显像过程中,患者取仰卧位。在检查的第18分钟静脉注射速尿作为利尿剂刺激剂。
一名8个月大的女性患者因咳嗽、呼吸急促(呼吸困难)、疲劳、恶心、呕吐和腹泻被转诊进行DTPA肾闪烁显像。这些症状在患者进行肾闪烁显像前十天出现。在此期间,患者一直在儿科接受治疗。患者接受了生化、超声和放射学检查。从尿培养中分离出铜绿假单胞菌。患者接受了七天的抗生素(阿米卡星)治疗,而在最后五天接受了沙丁胺醇和必嗽平治疗。体格检查时,我们发现左下腹有一个无触痛的造口,伴有肛门闭锁。通过DTPA肾闪烁显像,我们发现右肾缺如,左肾旋转不良,且排尿过程中存在严重问题。
单侧肾缺如通常不会产生任何重大健康问题,但在与其他先天性畸形相关的情况下,如现存肾脏旋转不良、肛门闭锁和心肺异常,可能会对生命造成非常严重的问题。
动态肾闪烁显像对于检测肾脏先天性畸形和功能异常是一种非常敏感且有用的方法。