婴儿饼脏:一个案例报告与文献综述
Rawa Bapir1,2,3, Wriya N Sabr1, Soran H Tahir1,4
1Scientific Affairs Department, Smart Health Tower, Madam Mitterrand Street, Sulaymaniyah 46001, Iraq.
Radiology case reports
|December 1, 2025
概括
饼脏 (PK) 是一种罕见的化脏异常. 这个案例突出了一个患有盆腔PK的婴儿,尿管盆腔结口阻塞,以及未下降的丸,这是一个非常罕见的组合.
科学领域:
- 儿科泌尿外科 儿科泌尿外科
- 遗传异常是一种先天性异常.
- 腎臟病學 (nephrology) 是一種醫學專業.
背景情况:
- 蛋 (PK) 是一种罕见的合异常 (2%的合),具有独特的解剖特征.
- 胰腺瘤可能与其他生殖尿路和全身异常有关.
- 这份报告详细介绍了一名婴儿,患有罕见的骨盆瘤结合,尿管骨盆结阻塞和未下降的丸.
研究的目的:
- 报告一个极为罕见的婴儿骨盆饼脏病例.
- 为了记录相关的异常,包括尿管皮层结口阻塞和未下降的丸.
- 审查现有的关于饼脏共同发生的文献.
主要方法:
- 一个2个月大的男婴的案例介绍.
- 诊断成像包括超声波和逆行热图.
- 在过去十年中对10例蛋糕脏病例的文献综述.
主要成果:
- 婴儿呈现出一个未下降的右丸和盆腔脏与恶性旋转.
- 诊断出左尿管盆结口阻塞,并用JJ支架进行治疗.
- 文献审查显示,在PK病例中男性占主导地位 (70%),并与UPJ阻塞和未下降的丸有共同的关联.
结论:
- 饼脏可以在婴儿中呈现一种罕见的异常星座.
- 早期诊断和管理对于UPJ阻塞和未下降的丸等相关疾病至关重要.
- 保守的管理与监测是无症状PK的一个选择.
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