Benson Michael, Lee Sang, Bhattacharya Ratul, Vasy Valentino, Zuberi Jamshed, Yasmeen Sayeeda, Ahmed Mutahar, Hanna Moneer K
Division of Urology, Rutgers New Jersey Medical School, Newark, NJ.
Saint George's University, Grenada.
Urology. 2018 Oct;120:211-215. doi: 10.1016/j.urology.2018.06.042. Epub 2018 Jul 10.
To discuss the presenting features, imaging findings, and recommended management of patients with Metanephric adenoma (MA) focusing on the diagnostic challenges and indications for follow up.
In this case report, we present a case of a 10-year-old female with MA who eventually underwent nephron sparing surgery with a partial nephrectomy. We performed a literature review of previous cases of metanephric adenoma and their respective management and follow-up.
Renal ultrasound demonstrated a heterogeneous, echogenic mass measuring 3.8 cm at the upper pole of the right kidney. Further investigations consisted of computed tomography scan, magnetic resonance imaging, and magnetic resonance angiography. The patient underwent robotic-assisted partial nephrectomy. The immunohistochemical staining pattern, gross, and microscopic appearance of the lesion were consistent with the diagnosis of MA. The combination of CK7, EMA, and S-100 negativity and WT1 and CD57 positivity is considered characteristic of metanephric adenoma as described in the literature.
MA is a rare benign tumor and especially in the pediatric population can cause significant concern over a possible malignant lesion. Although, no follow-up recommendations currently exist in cases of completely resected MA, we standardly perform postoperative surveillance. Although Metanephric Adenoma is difficult to diagnose preoperatively, given the advances in nephron sparing surgery and the utilization of nonionizing radiation modalities for follow up, we can manage these patients safely and with lower morbidity by preserving renal parenchyma.
探讨后肾腺瘤(MA)患者的临床表现、影像学表现及推荐的治疗方法,重点关注诊断挑战和随访指征。
在本病例报告中,我们呈现了一例10岁患有MA的女性病例,该患者最终接受了保留肾单位的部分肾切除术。我们对既往后肾腺瘤病例及其各自的治疗和随访情况进行了文献综述。
肾脏超声显示右肾上极有一个大小为3.8 cm的不均匀回声团块。进一步检查包括计算机断层扫描、磁共振成像和磁共振血管造影。患者接受了机器人辅助部分肾切除术。病变的免疫组化染色模式、大体和显微镜下表现与MA的诊断一致。如文献所述,CK7、EMA和S-100阴性以及WT1和CD57阳性的组合被认为是后肾腺瘤的特征。
MA是一种罕见的良性肿瘤,尤其是在儿童人群中,可能会引起对可能的恶性病变的严重关注。尽管目前对于完全切除的MA病例尚无随访建议,但我们通常会进行术后监测。尽管后肾腺瘤术前难以诊断,但鉴于保留肾单位手术的进展以及使用非电离辐射方式进行随访,我们可以通过保留肾实质安全地管理这些患者,并降低发病率。