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侵袭肾脏的神经母细胞瘤。

Neuroblastoma invading the kidney.

作者信息

Albregts A E, Cohen M D, Galliani C A

机构信息

Department of Radiology, James Whitcomb Riley Hospital For Children, Indiana University Medical Center, Indianapolis 46202-5200.

出版信息

J Pediatr Surg. 1994 Jul;29(7):930-3. doi: 10.1016/0022-3468(94)90018-3.

Abstract

Renal invasion by neuroblastoma is probably more common than is generally recognized. In this study, the incidence of renal parenchymal tumor invasion was 20.4% (10 patients) among 49 cases of abdominal neuroblastoma. Generally, the renoinfiltrative neuroblastomas were extensive and had unfavorable histological features as well as lymph node involvement; they were either stage III or IV. Tumor invasion occurred by direct penetration through the renal capsule and/or lymphatic perivascular spread. Imaging studies had 100% sensitivity and 94.9% specificity for detecting renal invasion of neuroblastoma. Surgery/pathology was the standard of reference. Two instances of misdiagnoses of renal invasion were attributed to inadequate resolution of older computed tomography films, partial volume effects, and renal distortion by tumor compression.

摘要

神经母细胞瘤侵犯肾脏的情况可能比普遍认为的更为常见。在本研究中,49例腹部神经母细胞瘤患者中,肾实质肿瘤侵犯的发生率为20.4%(10例患者)。一般来说,浸润肾脏的神经母细胞瘤范围广泛,具有不良的组织学特征且伴有淋巴结受累;它们多为Ⅲ期或Ⅳ期。肿瘤侵犯是通过直接穿透肾包膜和/或淋巴管周围血管扩散发生的。影像学检查在检测神经母细胞瘤肾脏侵犯方面的敏感性为100%,特异性为94.9%。手术/病理检查是参考标准。两例肾脏侵犯的误诊归因于旧的计算机断层扫描胶片分辨率不足、部分容积效应以及肿瘤压迫导致的肾脏变形。

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