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儿童膀胱神经母细胞瘤的罕见表现:一例报告。

Unusual presentation of bladder neuroblastoma in a child: A case report.

作者信息

Cai Jia-Bin, Wang Jin-Hu, He Min, Wang Fa-Liang, Xiong Jie-Ni, Mao Jun-Qing, Li Min-Ju, Zhu Kun, Liang Jia-Wei

机构信息

Division of Surgical Oncology, Department of Pediatric Surgery, Children's Hospital, Zhejiang University School of Medicine; National Clinical Research Center for Child Health, Hangzhou 310053, Zhejiang Province, China.

Department of Pathology, Children's Hospital, Zhejiang University School of Medicine; National Clinical Research Center for Child Health, Hangzhou 310053, Zhejiang Province, China.

出版信息

World J Clin Cases. 2020 Jan 6;8(1):194-199. doi: 10.12998/wjcc.v8.i1.194.

Abstract

BACKGROUND

Neuroblastoma is an extracranial malignant tumor in children that is most often located in the adrenal gland and sympathetic ganglion. Here, we present a rare case of neuroblastoma originating from the urinary bladder.

CASE SUMMARY

A 3-year-old girl presented with lower abdominal pain with micturition. Ultrasound revealed a lower abdominal mass. Abdominal computed tomography scan displayed a solitary mass at the top of the urinary bladder. Blood levels of neuron-specific enolase and lactate dehydrogenase were elevated. We treated the child with partial cystectomy and six courses of chemotherapy, and the outcome at 4-year follow-up was unremarkable.

CONCLUSION

Neuroblastoma should be considered when tumors are located in the urinary bladder, especially in the dome; although this presentation is rare, the prognosis is very good.

摘要

背景

神经母细胞瘤是儿童期一种颅外恶性肿瘤,最常位于肾上腺和交感神经节。在此,我们报告一例罕见的起源于膀胱的神经母细胞瘤病例。

病例摘要

一名3岁女孩出现排尿时下腹部疼痛。超声检查发现下腹部有一肿块。腹部计算机断层扫描显示膀胱顶部有一个孤立性肿块。神经元特异性烯醇化酶和乳酸脱氢酶的血液水平升高。我们对该患儿进行了部分膀胱切除术和六个疗程的化疗,4年随访结果无异常。

结论

当肿瘤位于膀胱,尤其是膀胱顶部时,应考虑神经母细胞瘤;尽管这种表现罕见,但预后非常好。

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引用本文的文献

本文引用的文献

1
Pediatric bladder neuroblastoma: Case report and literature review.
Can Urol Assoc J. 2013 Sep-Oct;7(9-10):E609-11. doi: 10.5489/cuaj.183.
2
Infantile neuroblastoma of the urinary bladder detected by hematuria.
Pediatr Surg Int. 2013 Jul;29(7):753-7. doi: 10.1007/s00383-013-3305-9. Epub 2013 Mar 31.
3
The International Neuroblastoma Risk Group (INRG) classification system: an INRG Task Force report.
J Clin Oncol. 2009 Jan 10;27(2):289-97. doi: 10.1200/JCO.2008.16.6785. Epub 2008 Dec 1.
4
The urinary bladder: An extremely rare location of pediatric neuroblastoma.
J Pediatr Surg. 2003 Aug;38(8):E10-2. doi: 10.1016/s0022-3468(03)00291-4.
5
Neuroblastoma of the urinary bladder in an infant clinically detected by hematuria.
Med Pediatr Oncol. 2000 Nov;35(5):488-92. doi: 10.1002/1096-911x(20001101)35:5<488::aid-mpo8>3.0.co;2-e.
6
Urachal tumor: an unusual presentation of neuroblastoma.
Pediatr Hematol Oncol. 2000 Jul-Aug;17(5):435-7. doi: 10.1080/08880010050034418.
7
Urachal neuroblastoma: first case report.
Pediatr Radiol. 1999 May;29(5):320-1. doi: 10.1007/s002470050597.
8
Neuroblastoma of the urinary bladder, preclinically detected by mass screening.
Pediatrics. 1999 May;103(5):e67. doi: 10.1542/peds.103.5.e67.
9
Bladder origin neuroblastoma detected by mass screening.
Urology. 1998 Dec;52(6):1139-41. doi: 10.1016/s0090-4295(98)00294-5.
10
Revisions of the international criteria for neuroblastoma diagnosis, staging, and response to treatment.
J Clin Oncol. 1993 Aug;11(8):1466-77. doi: 10.1200/JCO.1993.11.8.1466.

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