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急性肾盂肾炎和肾包膜下血肿提示肾母细胞瘤。

Acute pyelonephritis and subcapsular hematoma revealing a nephroblastoma.

作者信息

Benbrahim Fatima Zohra, Haddad Siham El, Belkouchi Lina, Faraj Chaymae, Jellal Sanae, Boutaleb Joud, Allali Nazik, Chat Latifa

机构信息

Department of Radiology, Children hospital of Rabat, Ibn Sina University Hospital, Mohammed V University, Rabat, Morocco.

出版信息

Radiol Case Rep. 2024 Nov 6;20(1):550-555. doi: 10.1016/j.radcr.2024.10.093. eCollection 2025 Jan.

DOI:10.1016/j.radcr.2024.10.093
PMID:39559506
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11570898/
Abstract

Nephroblastoma tumor is the most common renal tumor in children aged 1 to 5 years, typically presenting as an abdominal mass. However, other nonspecific signs may also reveal the disease. An unusual presentation, such as acute pyelonephritis or a subcapsular renal hematoma, is rarely an initial warning sign and should prompt investigation of an underlying cause, especially in the absence of trauma history. We report here a particular case of Wilms tumor, revealed by acute pyelonephritis and complicated by a subcapsular hematoma in a 6-year-old girl. We emphasize the importance of considering the diagnosis of Wilms tumor in any child presenting with renal hemorrhage, to improve prognosis and initiate therapeutic management as early as possible.

摘要

肾母细胞瘤是1至5岁儿童最常见的肾脏肿瘤,通常表现为腹部肿块。然而,其他非特异性体征也可能提示该病。不寻常的表现,如急性肾盂肾炎或肾包膜下血肿,很少是最初的警示信号,应促使对潜在病因进行调查,尤其是在没有外伤史的情况下。我们在此报告一例特殊的威尔姆斯瘤病例,该病例由急性肾盂肾炎发现,并伴有一名6岁女孩的肾包膜下血肿。我们强调,对于任何出现肾出血的儿童,考虑威尔姆斯瘤的诊断非常重要,以改善预后并尽早开始治疗管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/03e93bc995d7/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/e883459c40be/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/417ef25ee12c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/ab59da4b14af/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/03e93bc995d7/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/e883459c40be/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/417ef25ee12c/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/ab59da4b14af/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d777/11570898/03e93bc995d7/gr4.jpg

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引用本文的文献

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本文引用的文献

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Pedunculated and obstructive Wilms' tumor: A rare presentation in a 2 year-old male.带蒂梗阻性肾母细胞瘤:一名2岁男性患儿的罕见病例。
Urol Case Rep. 2018 Jun 7;20:38-40. doi: 10.1016/j.eucr.2018.06.004. eCollection 2018 Sep.
2
Bilateral Wilms tumour: a review of clinical and molecular features.双侧肾母细胞瘤:临床与分子特征综述
Expert Rev Mol Med. 2017 Jul 18;19:e8. doi: 10.1017/erm.2017.8.
3
Spontaneous rupture of adult Wilms' tumor: A case report and review of the literature.成人肾母细胞瘤自发性破裂:一例报告并文献复习
Can Urol Assoc J. 2015 Jul-Aug;9(7-8):E531-4. doi: 10.5489/cuaj.2539.
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Current surgical standards of care in Wilms tumor.肾母细胞瘤当前的外科护理标准。
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Detection of preoperative wilms tumor rupture with CT: a report from the Children's Oncology Group.CT 检测术前肾母细胞瘤破裂:来自儿童肿瘤协作组的报告。
Radiology. 2013 Feb;266(2):610-7. doi: 10.1148/radiol.12120670. Epub 2012 Nov 28.
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Urogenital tumours in childhood.儿童泌尿生殖系统肿瘤。
Cancer Imaging. 2011 Oct 3;11 Spec No A(1A):S48-64. doi: 10.1102/1470-7330.2011.9009.
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Preoperative Wilms tumor rupture: a retrospective study of 57 patients.术前肾母细胞瘤破裂:57例患者的回顾性研究
Cancer. 2008 Jul 1;113(1):202-13. doi: 10.1002/cncr.23535.
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Coagulopathy as a presenting feature of Wilms tumour.凝血功能障碍作为肾母细胞瘤的一种表现特征。
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