Department of Radiology, Qingdao Women and Children's Hospital, Qingdao, Shandong, 266000, China; Shandong Key Laboratory of Digital Medicine and Computer Assisted Surgery, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.
Department of Abdominal Ultrasound, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.
Clin Imaging. 2021 Apr;72:91-96. doi: 10.1016/j.clinimag.2020.10.040. Epub 2020 Nov 4.
Congenital mesoblastic nephroma (CMN) is a rare renal tumor mainly observed in infants and young children. This study aims to analyze the imaging manifestations of CMN to improve the understanding of the disease.
The imaging manifestations and clinical records of all pediatric patients with CMN admitted to our hospital over the last 7 years were retrospectively analyzed. The diagnosis of CMN was confirmed by postoperative pathology. All patients underwent computed tomography (CT) scans; 2 patients additionally underwent magnetic resonance imaging (MRI) scans (including one prenatal MRI scan).
We evaluated 10 pediatric patients (6 males and 4 females) aged 7 days to 12 months (median age: 4 months) with CMN located on the left kidney in six cases and the right kidney in four cases. The CT imaging manifested as solid lesions (5 cases), solid-cystic lesions with solid predominance (4 cases), or solid-multicystic lesions with cystic predominance (1 case). Enhanced CT showed moderately and heterogeneously enhanced solid component and intracystic septations at the corticomedullary phase that were further enhanced at the nephrographic phase, although their CT values were still lower than those of the renal parenchyma. The "double-layer sign" were seen in 4 cases of classic type of CMN, and the "intratumor pelvis sign" were seen in 9 cases that include 5 classic, 3 cellular and 1 mixed type of CMN. In the 2 patients who underwent MRI, the scans showed solitary masses. The lesions had hypointense signals on the T1WI sequence and isointensity or slightly lower-intensity signals than the surrounding renal parenchyma on the fluid-sensitive sequences, whereas the lesions showed hyperintense signals on the diffusion-weighted imaging (DWI) sequence.
The imaging manifestations of CMN are closely correlated with the pathological subtype and have certain characteristics. The "double-layer sign" was seen with most classic type CMN, and "intratumor pelvis sign" was seen in 90% cases.
先天性中胚层肾瘤(CMN)是一种主要发生于婴儿和幼儿的罕见肾肿瘤。本研究旨在分析 CMN 的影像学表现,以提高对该疾病的认识。
回顾性分析了过去 7 年来我院收治的所有小儿 CMN 患者的影像学表现和临床记录。CMN 的诊断通过术后病理证实。所有患者均行 CT 扫描;2 例患者另外行 MRI 扫描(包括 1 例产前 MRI 扫描)。
我们评估了 10 例小儿患者(6 男 4 女),年龄 7 天至 12 个月(中位年龄:4 个月),CMN 位于左肾 6 例,右肾 4 例。CT 影像学表现为实性病变(5 例)、实性为主的囊实性病变(4 例)或囊性为主的多房实性病变(1 例)。增强 CT 显示皮质髓质期实质部分中度和不均匀强化,囊内分隔进一步强化,虽然其 CT 值仍低于肾实质。4 例经典型 CMN 可见“双层征”,9 例可见“瘤内肾盂征”,其中包括 5 例经典型、3 例细胞型和 1 例混合型 CMN。在 2 例行 MRI 的患者中,扫描显示为单发肿块。病变在 T1WI 序列上呈低信号,在液体敏感序列上与周围肾实质等信号或稍低信号,而在弥散加权成像(DWI)序列上呈高信号。
CMN 的影像学表现与病理亚型密切相关,具有一定特征。大多数经典型 CMN 可见“双层征”,90%的病例可见“瘤内肾盂征”。