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本文引用的文献

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Synchronous carotid body and thoracic paraganglioma associated with a germline SDHC mutation.与种系 SDHC 突变相关的颈动脉体和胸内副神经节瘤的同步发生。
J Vasc Surg. 2011 Mar;53(3):805-7. doi: 10.1016/j.jvs.2010.09.064. Epub 2010 Nov 23.
2
A case of large "silent" extra-adrenal retroperitoneal paraganglioma resected laparoscopically.1例经腹腔镜切除的巨大“无症状”肾上腺外腹膜后副神经节瘤
Chin Med Sci J. 2010 Mar;25(1):61-4. doi: 10.1016/s1001-9294(10)60023-5.
3
Bilateral pheochromocytoma associated with paraganglioma and papillary thyroid carcinoma: report of an unusual case.双侧嗜铬细胞瘤合并副神经节瘤及甲状腺乳头状癌:1例罕见病例报告
Endocr J. 2007 Apr;54(2):227-31. doi: 10.1507/endocrj.k06-068. Epub 2007 Jan 31.
4
Malignant pheochromocytomas and paragangliomas: a phase II study of therapy with high-dose 131I-metaiodobenzylguanidine (131I-MIBG).恶性嗜铬细胞瘤和副神经节瘤:高剂量131I-间碘苄胍(131I-MIBG)治疗的II期研究
Ann N Y Acad Sci. 2006 Aug;1073:465-90. doi: 10.1196/annals.1353.050.
5
[Paragangliomas: clinical and secretory profile. Result of 39 cases].[副神经节瘤:临床与分泌特征。39例病例结果]
Ann Chir. 2005 Mar;130(3):157-61. doi: 10.1016/j.anchir.2004.12.001. Epub 2004 Dec 23.
6
Preaortic paraganglioma mimicking a hypervascular tumor of the pancreas.酷似胰腺高血运肿瘤的主动脉前副神经节瘤。
Hepatogastroenterology. 2004 Jul-Aug;51(58):1198-201.
7
Case report: patient with multiple paragangliomas treated with long acting somatostatin analogue.病例报告:使用长效生长抑素类似物治疗的多发副神经节瘤患者。
Endocr J. 2003 Oct;50(5):507-13. doi: 10.1507/endocrj.50.507.
8
Neurogenic tumors in the abdomen: tumor types and imaging characteristics.腹部神经源性肿瘤:肿瘤类型及影像学特征
Radiographics. 2003 Jan-Feb;23(1):29-43. doi: 10.1148/rg.231025050.
9
[Retroperitoneal non-secreting paraganglioma].[腹膜后无分泌功能的副神经节瘤]
J Radiol. 1999 Feb;80(2):150-2.
10
Pheochromocytoma of urinary bladder: contemporary methods of diagnosis and treatment options.膀胱嗜铬细胞瘤:当代诊断方法与治疗选择
Urology. 1993 May;41(5):435-9. doi: 10.1016/0090-4295(93)90503-3.

表现为胰腺肿块并伴有膀胱副神经节瘤的腹膜后非功能性副神经节瘤:一种极其罕见的病例。

Non-functional paraganglioma of retroperitoneum mimicking pancreatic mass with concurrent urinary bladder paraganglioma: an extremely rare entity.

作者信息

Verma Ankur, Pandey Diwakar, Akhtar Azaz, Arsia Ashish, Singh Nain

机构信息

Senior Resident, Department of Surgery, Lady Harding Medical College and SSKH , New Delhi, India .

Post graduate Student, Department of Surgery, Lady Harding Medical College and SSKH , New Delhi, India .

出版信息

J Clin Diagn Res. 2015 Feb;9(2):XD09-XD11. doi: 10.7860/JCDR/2015/11156.5570. Epub 2015 Feb 1.

DOI:10.7860/JCDR/2015/11156.5570
PMID:25859512
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4378794/
Abstract

Paragangliomas are extra-adrenal tumours of the autonomic nervous system, which rarely present as primary retroperitoneal mass mimicking pancreatic malignancy (incidence 2-8 per million populations). Urinary Bladder Paraganglioma are also extremely rare (0.06% of all Bladder Tumour and 6% of Paragangliomas) with most being malignant and high grade tumours. Non-functional varieties of both tumours are usually incidentally diagnosed. The possibility for malignant transformation in them makes surgical excision the treatment of choice. A 45-year-old lady with abdominal pain was investigated to have a complex retroperitoneal mass behind head of pancreas and a urinary bladder mass. Complete excision of retroperitoneal and bladder lesion was done. Histopathological examinations of both specimens were suggestive of Paraganglioma with no abnormal mitotic activity and capsular/vascular invasion. Although concurrent non functional paragangliomas had been reported but the synchronous non-functional paragangliomas of retroperitoneum and urinary bladder reported in this case is extremely rare and is not reported so far in English literature.

摘要

副神经节瘤是自主神经系统的肾上腺外肿瘤,很少表现为模仿胰腺恶性肿瘤的原发性腹膜后肿块(发病率为每百万人口2 - 8例)。膀胱副神经节瘤也极为罕见(占所有膀胱肿瘤的0.06%,占副神经节瘤的6%),大多数为恶性和高级别肿瘤。这两种肿瘤的无功能型通常是偶然诊断出来的。它们发生恶性转化的可能性使得手术切除成为首选治疗方法。一名45岁腹痛女性接受检查,发现胰腺头部后方有一个复杂的腹膜后肿块以及一个膀胱肿块。对腹膜后和膀胱病变进行了完整切除。两个标本的组织病理学检查均提示为副神经节瘤,无异常有丝分裂活动及包膜/血管侵犯。虽然已有并发无功能副神经节瘤的报道,但本例中腹膜后和膀胱同时出现的无功能副神经节瘤极为罕见,英文文献中迄今尚未见报道。