期刊文献+

前列腺副神经节瘤1例报道并文献复习 被引量:2

Paraganglioma of the prostate:A case report and review of the literature
下载PDF
导出
摘要 目的:探讨前列腺副神经节瘤的临床表现、病理特征、治疗和预后。方法:报道前列腺副神经节瘤1例,患者男,39岁,主因"反复血精1年余"入院,误诊为前列腺癌后,行耻骨上前列腺根治性切除术,完整切除肿瘤。结果:术后病理确诊为前列腺副神经节瘤,本例前列腺副神经节瘤为无功能性,免疫组化:NSE(+)、CGA(+)、S100(+)、CK(-)、Desmin(-)。术后血压平稳,2周后拔尿管出院。随访48个月至今未复发。结论:前列腺副神经节瘤缺乏特异的临床特征表现,易误诊,只有靠切除术后病理和免疫组化才能确诊。由于其非常罕见,相关治疗缺乏成熟的经验,故需要进一步研究。 Objective: To investigate the clinical presentation, pathologic features, treatment and prognosis of prostatic para- ganglioma. Methods : We retrospectively studied a case of prostatic paraganglioma and reviewed relevant literature. The patient was a 39-year-old man, admitted for repeated hemaspermia for over 12 months. After misdiagnosed as having prostate cancer, he underwent suprapubic prostatectomy, with the tumor completely removed. Results: Postoperative pathological examination confirmed the tumor to be prostatic paraganglioma, which was non-functional, with the immunohistochemical results of NSE ( + ), CGA ( + ), S100 ( + ), CK ( - ) and Desmin ( - ). Postoperative blood pressure was stable. Two weeks after surgery, the urethral catheter was removed and the patient discharged. No recurrence was found during 48 months of follow-up. Conclusion: Lacking specific clinical characteristics, paraganglioma of the prostate is easily misdiagnosed, and can be confirmed only by postoperative pathology and immunohistochemistry. For the treatment of this rare tumor, little experience has been accumulated, and further studies are needed.
出处 《中华男科学杂志》 CAS CSCD 2012年第8期715-718,共4页 National Journal of Andrology
关键词 前列腺肿瘤 副神经节瘤 手术切除 病理 免疫组化 prostate cancer paraganglioma surgery pathology immunohistochemistry
  • 相关文献

参考文献21

  • 1Mehta M, Nadel N S, Lonni Y, et al. Malignant paraganglonma of the prostate and retroperitoneum. J Urol, 1979, 121 (3): 376 -378.
  • 2Boyle M, Gaffney EF, Thurston A. Paraganglioma of the prostatic urethra. A report of three cases and a review of the literature. Br J Urol, 1996, 77(3) : 445-448.
  • 3Hasselager T, Horn T, Rasmussen F. Paraganglioma of the pros- tate. A case report and review of the literature. Scand J Urol Nephrol, 1997, 31(5): 501-503.
  • 4Denford A, Vaughan M, Mayall. Paraganglioma as an unusual mim- ic of carcinoma in the prostate. Br J Urol, 1997, 30(4) : 677- 678.
  • 5Shapiro B, Gonzalez E, Weissman A, et al. Malignant paragan- glinma of the prostate: Case report, depiction by meta-iodo- benzylguanidine scintigraphy and review of the literature. Q J Nu- cl Med, 1997, 41 ( 1 ) : 36-41.
  • 6Jimenez RE, Tiguert R, Harb JF. Prostatic paraganglioma: 5- year follow-up. J Urol, 1999, 161(6): 1909-1910.
  • 7Campodonico F, Bandelloni R, Maffezzini M. Paraganglioma of the prostate in a young adult. Urology, 2005, 66 (3) : 657.
  • 8Li QK, MacLennan GT. Paraganglioma of the prostate. J Urol,2006, 175(1) : 314.
  • 9陈朝晖,杨郁,肖亚军,杜茂信,肖传国.前列腺副神经节瘤(附二例报告)[J].中华泌尿外科杂志,2003,24(5):331-333. 被引量:6
  • 10杨长滨,韩艳茹.前列腺恶性嗜铬细胞瘤1例[J].实用肿瘤学杂志,2004,18(4):274-274. 被引量:4

二级参考文献23

  • 1冀强,蒋力生,陈鹏.腹膜后副神经节瘤的组织学和临床研究(附10例报告)[J].四川解剖学杂志,2004,12(4):272-273. 被引量:6
  • 2Somasundar P, Krouse R, Hostetter R, et al. Paraganglioma-a decade of clinical experience. J Surg Oncol, 2000, 74: 286-290.
  • 3陈创奇,李穗生,刘唐彬.膀胱恶性化学感受器瘤1例[J].中华小儿外科杂志,1997,18(1):44-44. 被引量:4
  • 4Boyle M, Gaffney EF,Thurston A. Paraganglioma of the prostatic urethra. A report of three cases and a review of the literature. Br J Urol,1996.77:445 -448.
  • 5Jimenez RE, Tiguert R, Harb JF. Prostatic paraganglioma:5-year followuo. J Urol. 1999.161 : 1909-1910.
  • 6Grignon DJ, Ro JY, Mackay B, et al. Paraganglioma of the urinary bladder: immunohistochemical, uhrastructural, and DNA flow cytometric studies. Hum Pathol, 1991,22 : 1162-1169.
  • 7Cheng L, Leibovich BC, Cheville JC, et al. Paraganglioma of the urinary bladder:can biologic potential be predicted? Cancer, 2000,88:844-852.
  • 8Landas SK, Leigh C, Bonsib SM, et al. Occurrence of melanin in pheochromocytoma. Mod Pathol, 1993,6:175-178.
  • 9Lamovec J, Frkovic-Grazio S, Bracko M. Nonsporadic cases and unusual morphological features in pheochromocytoma and paraganglioma. Arch Pathol Lab Med, 1998,122:63-68.
  • 10Thompson LD. Pheochromocytoma of the Adrenal gland Scaled Score( PASS ) to separate benign from malignant neoplasms: a clinicopathologic and immunophenotypic study of 100 cases. Am J Surg Pathol, 2002,26:551-566.

共引文献55

同被引文献33

  • 1黄裕,邹冬玲,姜青明,王冬.阴道副神经节瘤1例报告并文献复习[J].肿瘤防治研究,2014,41(5):513-514. 被引量:1
  • 2Ahmad S, Cathy D, Sheikh M, et al. Retroperitoneal extra adrenal paraganglioma: a rare hut important diagnosis[J]. Ir J Med Sci,2009,178(2) :211- 214.
  • 3Disick GI, Palese MA. Extra-adrenal pheochromocytoma., di- agnosis and management[J]. Curt Urol Rep,2007,8(1) : 83- 88.
  • 4Baez JC, Jagannathan JP, Krajewski K, et al. Pheochromo- cytoma and paraganglioma: imaging characteristics[J]. Canc- er Imaging, 2012,12 : 153-162.
  • 5Nieto Palacios A, Martinez Alvarez R, del Barco Morillo E. Other therapeutic alternatives: radiotherapy and chemothera- py[J]. Acta Otorrinolaringol Esp, 2009,60 Suppl 1 : 130-136.
  • 6Strauss DC, Hayes AJ, Thomas JM. Retroperitoneal tumours: re- view of management[J]. Ann R Coil Surg Engl,2011,93(4) 275-280.
  • 7Wachtel H, Cerullo I, Bartlett EK, et al. Clinicopathologic characteristics of incidentally identified pheochromocytoma [J]. Ann Surg Oncol,2015,22(1):132-138.
  • 8Warner KI, Poole-Ward RL, Martinez A, et al. Postpartum transabdominal laparoscopic adrenalectomy for pheochromo- cytoma presenting with abruption and hypertensive emergen-cy[J]. Am Surg,2015,81(1) :E34 -35.
  • 9Misra MC, Bhattacharjee HK, Hemal AK, et al. Laparo- scopic management of rare retroperitoneal tumors[J]. Surg Laparosc Endosc Percutan Tech, 2010,20(3) : e117-122.
  • 10Joynt KE, Moslehi JJ, Baughman KL. Paragangliomas: eti- ology, presentation, and management[J]. Cardiol Rev, 2009, 17(4) : 159-164.

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部