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妊娠合并双侧嗜铬细胞瘤1例报告 |
任翔1, 尚吉文2, 张华俊2, 马丁2, 姚雪2 |
1山西医科大学附属白求恩医院泌尿外科 030032 太原;
2山西白求恩医院泌尿外科 |
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Bilateral pheochromocytoma in pregnancy: One case report and review of literatures |
REN Xiang1, SHANG Jiwen2, ZHANG Huajun2, MA Ding2, YAO Xue2 |
1Department of Urology, Bethune Hospital, Shanxi Medical University, Taiyuan 030032, China;
2Department of Urology, Shanxi Bethune Hospital |
引用本文: |
任翔, 尚吉文, 张华俊, 马丁, 姚雪. 妊娠合并双侧嗜铬细胞瘤1例报告[J]. 微创泌尿外科杂志, 2021, 10(2): 133-136.
REN Xiang, SHANG Jiwen, ZHANG Huajun, MA Ding, YAO Xue. Bilateral pheochromocytoma in pregnancy: One case report and review of literatures. JOURNAL OF MINIMALLY INVASIVE UROLOGY, 2021, 10(2): 133-136.
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链接本文: |
http://journal20.magtechjournal.com/Jwk_zgmnwk/CN/abstract/abstract1669.shtml 或 http://journal20.magtechjournal.com/Jwk_zgmnwk/CN/Y2021/V10/I2/133 |
[1] LENDERS JW, EISENHOFER G, MANNELLI M, et al.Phaeochromocytoma. Lancet, 2005,366(9486):665-675.
[2] VAN DER WEERD K, VAN NOORD C, LOEVE M, et al. ENDOCRINOLOGY IN PREGNANCY: Pheochromocytoma in pregnancy: case series and review of literature. Eur J Endocrinol, 2017,177(2):R49-R58.
[3] SARATHI V, LILA AR, BANDGAR TR, et al.Pheochromocytoma and pregnancy: a rare but dangerous combination. Endocr Pract, 2010,16(2):300-309.
[4] PHUPONG V, WITOONPANICH P, SNABBOON T, et al.Bilateral pheochromocytoma during pregnancy. Arch Gynecol Obstet, 2005,271(3):276-279.
[5] MOHAMED ISMAIL NA, ABD RAHMAN R, ABD WAHAB N, et al.Pheochromocytoma and pregnancy: a difficult and dangerous ordeal. Malays J Med Sci, 2012,19(1):65-68.
[6] SCHREINEMAKERS JM, ZONNENBERG BA, HÖPPENER JW, et al. A patient with bilateral pheochromocytoma as part of a Von Hippel-Lindau (VHL) syndrome type 2C. World J Surg Oncol, 2007,5(1):112.
[7] GÓMEZ AM, SOARES DC, COSTA AAB, et al. Pheochromocytoma and paraganglioma: implications of germline mutation investigation for treatment, screening, and surveillance. Arch Endocrinol Metab, 2019,63(4):369-375.
[8] SNABBOON T, PLENGPANICH W, HOUNGNGAM N, et al.Concurrent bilateral pheochromocytoma and thoracic paraganglioma during pregnancy. Endocrine, 2010,37(2):261-264.
[9] WATTANACHANYA L, BUNWORASATE U, PLENGPANICH W, et al.Bilateral pheochromocytoma during the postpartum period. Arch Gynecol Obstet, 2009,280(6):1055-1058.
[10] KITAYAMA K, KASHIWAGI S, AMANO R, et al.A case of bilateral pheochromocytoma during pregnancy. BMC Surg, 2015,15(1):55.
[11] CHMIELEWSKI G, WALCZYK A, KOWALSKA A.Two cases of pheochromocytoma in pregnancy: a multidisciplinary challenge. Endokrynol Pol, 2020,71(1):98-99.
[12] 张创标,卢筱华,冯烈.妊娠并双侧肾上腺嗜铬细胞瘤误诊探讨.临床误诊误治,2016,29(6):56-58.
[13] GOLSHEVSKY JR, KAREL K, TEALE G.Phaeochromocytoma causing acute pulmonary oedema during emergency caesarean section. Anaesth Intensive Care, 2007,35(3):423-427.
[14] GRIFFIN JB, NORMAN PF, DOUVAS SG, et al.Pheochromocytoma in pregnancy: diagnosis and collaborative management. South Med J, 1984,77(10):1325-1327.
[15] KALRA JK, JAIN V, BAGGA R, et al.Pheochromocytoma associated with pregnancy. J Obstet Gynaecol Res, 2003,29(5):305-308.
[16] PODOLSKY ER, FEO L, BROOKS AD, et al.Robotic resection of pheochromocytoma in the second trimester of pregnancy. JSLS, 2010,14(2):303-308.
[17] WERBEL SS, OBER KP.Pheochromocytoma. Update on diagnosis, localization, and management. Med Clin North Am, 1995,79(1):131-153.
[18] FISHBEIN L, MERRILL S, FRAKER DL, et al.Inherited mutations in pheochromocytoma and paraganglioma: why all patients should be offered genetic testing. Ann Surg Oncol, 2013,20(5):1444-1450.
[19] PANDIT R, KHADILKAR K, SARATHI V, et al.Germline mutations and genotype-phenotype correlation in Asian Indian patients with pheochromocytoma and paraganglioma. Eur J Endocrinol, 2016,175(4):311-323.
[20] ERLIC Z, RYBICKI L, PECZKOWSKA M, et al.Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients. Clin Cancer Res, 2009,15(20):6378-6385.
[21] LENDERS JW, DUH QY, EISENHOFER G, et al.Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. J Clin Endocrinol Metab, 2014,99(6):1915-1942.
[22] OPOCHER G, SCHIAVI F.Genetics of pheochromoeytomas and paragangliomas. Best Pract Res Clin Endocrinol Metab, 2010,24(6):943-956.
[23] CUI Q, LU J, ZHANG C, et al.Diagnostic challenges and good treatment outcomes in pediatric paraganglioma of the abdomen: A case report. Medicine (Baltimore), 2018,97(47):e13268-e13268.
[24] NEUMANN HP, YOUNG WF JR, KRAUSS T, et al.65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma. Endocr Relat Cancer, 2018,25(8):T201-T219.
[25] BURNICHON N, MAZZELLA JM, DRUI D, et al.Risk assessment of maternally inherited SDHD paraganglioma and phaeochromocytoma. J Med Genet, 2017,54(2):125-133. |
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