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偶然发现的盘状肾:一例报告。

Incidentally detected pancake kidney: a case report.

作者信息

Bakshi Sabyasachi

机构信息

Department of General surgery, BSMCH, Bankura, West Bengal, PIN-722102, India.

, Kathghara Lane,Sonatuli, Hooghly, 712103, West Bengal, India.

出版信息

J Med Case Rep. 2020 Aug 14;14(1):129. doi: 10.1186/s13256-020-02455-0.

Abstract

BACKGROUND

Congenital anomalies of the urinary system are very common and have extremely varied presentation. Among them, the most rarely found structural anomaly is the pancake kidney. When both kidneys are fused along their medial surfaces to form a round-shaped single renal mass, it is termed as pancake kidney. In this case report, a pancake kidney was incidentally detected in a girl. The majority of individuals who have pancake kidney are usually asymptomatic but surgeons should be aware of coexisting malformation of other organs and its potential risk of developing malignancy.

CASE PRESENTATION

A 12-year-old Bengali girl presented to our out-patient department with mild, dull aching, lower abdominal pain and dysuria. She had no history of fever, hematuria, menstrual abnormality, pelvic inflammatory disease, or trauma. Urine examination showed traces of albumin and 10-12 pus cells/high-power field. She had normal kidney function test but a digital X-ray of her kidney, ureter, and bladder region failed to demonstrate bilateral renal tissue shadows. Ultrasonography of her whole abdomen showed normal intra-abdominal organs except for empty bilateral renal fossa. A multi-detector computed tomography scan of her whole abdomen revealed one round-shaped mass measuring approximately 9 cm (vertical) × 10 cm (horizontal) in the pelvic cavity. That mass was finally identified as a pancake kidney. She was prescribed antibiotics based on urine culture and sensitivity test that cured her symptoms. She was advised to follow-up regularly in our out-patient department to evaluate her kidney function and to rule out any neoplastic change.

CONCLUSIONS

This condition can be managed conservatively, if the individual remains asymptomatic, by regular monitoring of renal function. Surgeons should remain alert for the development of infections, any obstructive manifestations leading to calculus formation, and any malignant changes. The individual should be careful in avoiding trauma to low-lying pelvic kidney. Extensive surgeries should be avoided and only selective procedures should be done so that the patient may lead a normal lifestyle.

摘要

背景

泌尿系统先天性异常非常常见,表现形式极为多样。其中,最罕见的结构异常是饼状肾。当双侧肾脏沿其内侧表面融合形成一个圆形的单一肾脏团块时,即称为饼状肾。在本病例报告中,一名女孩偶然被发现患有饼状肾。大多数患有饼状肾的个体通常无症状,但外科医生应注意其他器官是否存在合并畸形及其发生恶性肿瘤的潜在风险。

病例介绍

一名12岁的孟加拉女孩因下腹部轻度钝痛和排尿困难前来我院门诊就诊。她无发热、血尿、月经异常、盆腔炎或外伤史。尿液检查显示有微量白蛋白,每高倍视野有10 - 12个脓细胞。她的肾功能检查正常,但肾脏、输尿管和膀胱区域的数字X线检查未能显示双侧肾脏组织阴影。全腹部超声检查显示除双侧肾窝空虚外,腹内器官正常。全腹部多排螺旋CT扫描显示盆腔内有一个圆形团块,大小约为9厘米(垂直径)×10厘米(横径)。该团块最终被确定为饼状肾。根据尿培养和药敏试验结果给予她抗生素治疗,症状得以缓解。建议她定期来我院门诊随访,以评估肾功能并排除任何肿瘤性改变。

结论

如果个体无症状,这种情况可通过定期监测肾功能进行保守治疗。外科医生应警惕感染的发生、任何导致结石形成的梗阻性表现以及任何恶性变化。患者应注意避免对低位盆腔肾造成创伤。应避免进行广泛的手术,仅进行选择性手术,以便患者能够过上正常生活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/558d/7427080/f60e8acd55a5/13256_2020_2455_Fig1_HTML.jpg

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