成人多囊性发育不良肾脏:苏丹成年女性单侧发病的病例报告

IF 0.5 Q4 UROLOGY & NEPHROLOGY
Amer Abbo Hassan Abbo , Basil Amer Abbo Hassan , Amel Abdelrahman Omer Ibrahim
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引用次数: 0

摘要

多囊发育不良性肾脏是一种先天性畸形,通常在婴儿期确诊,在成人中罕见。我们的病例中,一名25岁的苏丹女性因左侧腹痛而就诊。影像学检查显示,左肾被囊肿和卵巢囊肿取代,符合多囊发育不良肾。她成功地接受了开放性单纯肾切除术;组织病理学证实为 MCDK。我们的病例凸显了成人 MCDK 在诊断和治疗方面的挑战。保守治疗的患者越来越多,尤其是无症状且对侧肾功能正常的患者。苏丹的医疗卫生障碍,包括认识不足和政治动荡,使及时诊断和治疗变得复杂。多学科护理和改善医疗服务至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multicystic dysplastic kidney in adults: A case report of unilateral presentation in an adult sudanese female

Multicystic dysplastic kidney is a congenital anomaly typically diagnosed in infancy, rare in adults, in our case of a 25-year-old Sudanese female presented with left flank pain. Imaging showed the left kidney replaced by cysts, consistent with MCDK, and ovarian cyst. She underwent a successful open simple nephrectomy; and histopathology confirmed MCDK. Our case highlights diagnostic and management challenges of MCDK in adults. Conservative management is increasing, especially for asymptomatic patients with normal contralateral kidney function. Healthcare barriers in Sudan, including limited awareness and political unrest, complicate timely diagnosis and treatment. Multidisciplinary care and improved healthcare access are essential.

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来源期刊
Urology Case Reports
Urology Case Reports Medicine-Urology
CiteScore
0.90
自引率
20.00%
发文量
325
审稿时长
37 days
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