国际肿瘤学杂志››2021,Vol. 48››Issue (10): 635-637.doi:10.3760/cma.j.cn371439-20201228-00125
收稿日期:
2020-12-28修回日期:
2021-03-18出版日期:
2021-10-08发布日期:
2021-11-24通讯作者:
王澜 E-mail:wlan2006@sina.com
Received:
2020-12-28Revised:
2021-03-18Online:
2021-10-08Published:
2021-11-24摘要:
睾丸恶性孤立性纤维性肿瘤临床报道非常少见,关于其生物学行为特点、适宜的治疗措施亦无成熟经验可借鉴,现就河北医科大学第四医院收治的1例术后放疗睾丸恶性孤立性纤维性肿瘤患者进行总结。
陈晓希, 丁妍, 王磊, 韩春, 王澜. 术后放疗睾丸恶性孤立性纤维性肿瘤一例[J]. 国际肿瘤学杂志, 2021, 48(10): 635-637.
[1] | Cerdá-Nicolás M, Löpez-Gines C, Gil-Benso R, et al. Solitary fibrous tumor of the orbit: morphological, cytogenetic and molecular features[J]. Neuropathology, 2006, 26(6):557-563. DOI: 10.1111/j.1440-1789.2006.00726.x. doi:10.1111/j.1440-1789.2006.00726.xpmid:17203593 |
[2] | 王坚, 朱雄增. 软组织肿瘤病理学(第2版)[M]. 北京: 人民卫生出版社, 2017: 318-330. |
[3] | Guillou L, Fletcher JA, Fletcher CDM, et al. Extrapleural solitary fibrous tumour and haemangiopericytoma[M]//Fletcher CDM, Unni KK, Mertens F, eds. World Health Organization classification of tumours. Pathology and genetics of tumours of soft tissue and bone. Lyon, France: IARC Press, 2002: 86-90. |
[4] | Vimi S, Punnya VA, Kaveri H, et al. An aggressive solitary fibrous tumor with evidence of malignancy: a rare case report[J]. Head Neck Pathol, 2008, 2(3):236-241. DOI: 10.1007/s12105-008-0073-2. doi:10.1007/s12105-008-0073-2pmid:20614322 |
[5] | 陈卉娇, 张红英, 李响, 等. 26例孤立性纤维性肿瘤临床病理及免疫组化特征[J]. 四川大学学报(医学版), 2004, 35(5):675-679. DOI: 10.3969/j.issn.1672-173X.2004.05.021 doi:10.3969/j.issn.1672-173X.2004.05.021 |
[6] | Kalebi AY, Hale MJ, Wong ML, et al. Surgically cured hypoglyce-mia secondary to pleural solitary fibrous tumour: case report and update review on the Doege-Potter syndrome[J]. J Cardiothorac Surg, 2009, 4:45. DOI: 10.1186/1749-8090-4-45. doi:10.1186/1749-8090-4-45pmid:19689813 |
[7] | Ruppe MD, Huang SA, Jan de Beur SM. Consumptive hypothyroi-dism caused by paraneoplastic production of type 3 iodothyronine deiodinase[J]. Thyroid, 2005, 15(12):1369-1372. DOI: 10.1089/thy.2005.15.1369. doi:10.1089/thy.2005.15.1369pmid:16405410 |
[8] | Han G, Zhang Z, Shen X, et al. Doege-Potter syndrome: a review of the literature including a new case report[J]. Medicine (Baltimore), 2017, 96(27):e7417. DOI: 10.1097/MD.0000000000007417. doi:10.1097/MD.0000000000007417 |
[9] | Geng H, Ye Y, Jin Y, et al. Malignant solitary fibrous tumor of the pancreas with systemic metastasis: a case report and review of the literature[J]. World J Clin Cases, 2020, 8(2):343-352. DOI: 10.12998/wjcc.v8.i2.343. doi:10.12998/wjcc.v8.i2.343pmid:32047784 |
[10] | 刘毅, 刘剑羽, 王宏磊, 等. 孤立性纤维性肿瘤的影像表现[J]. 中华放射学杂志, 2012, 46(5):441-444. DOI: 10.3760/cma.j.issn.1005-1201.2012.05.014. doi:10.3760/cma.j.issn.1005-1201.2012.05.014 |
[11] | 黄海建, 曲利娟, 郑智勇, 等. 恶性孤立性纤维性肿瘤4例临床病理分析[J]. 临床与实验病理学杂志, 2010, 26(6):724-727. DOI: 10.3969/j.issn.1001-7399.2010.06.023. doi:10.3969/j.issn.1001-7399.2010.06.023 |
[12] | Huang SC, Huang HY. Solitary fibrous tumor: an evolving and unifying entity with unsettled issues[J]. Histol Histopathol, 2019, 34(4):313-334. DOI: 10.14670/HH-18-064. doi:10.14670/HH-18-064 |
[13] | 黄海建, 曲利娟, 郑智勇. 孤立性纤维性肿瘤研究进展[J]. 现代肿瘤医学, 2011, 19(6):1255-1258. DOI: 10.3969/j.issn.1672-4992.2011.06.71. doi:10.3969/j.issn.1672-4992.2011.06.71 |
[14] | Weiss SW, Goldblum JR. Soft tissue tumors[M]. St Louis: Mosby Elsevier Press, 2008: 412, 949, 1121, 1129-1131. |
[15] | Mosquera JM, Fletcher CD. Expanding the spectrum of malignant progression in solitary fibrous tumors: a study of 8 cases with a discrete anaplastic component—is this dedifferentiated SFT?[J]. Am J Surg Pathol, 2009, 33(9):1314-1321. DOI: 10.1097/pas.0b013e3181a6cd33. doi:10.1097/pas.0b013e3181a6cd33 |
[16] | Sun Y, Naito Z, Ishiwata T, et al. Basic FGF and Ki-67 proteins useful for immunohistological diagnostic evaluations in malignant solitary fibrous tumor[J]. Pathol Int, 2003, 53(5):284-290. DOI: 10.1046/j.1440-1827.2003.01474.x. doi:10.1046/j.1440-1827.2003.01474.x |
[17] | Schweizer L, Koelsche C, Sahm F, et al. Meningeal hemangiopericytoma and solitary fibrous tumors carry the NAB2-STAT6 fusion and can be diagnosed by nuclear expression of STAT6 protein[J]. Acta Neuropathol, 2013, 125(5):651-658. DOI: 10.1007/s00401-013-1117-6. doi:10.1007/s00401-013-1117-6pmid:23575898 |
[18] | Akaike K, Kurisaki-Arakawa A, Hara K, et al. Distinct clinicopa-thological features of NAB2-STAT6 fusion gene variants in solitary fibrous tumor with emphasis on the acquisition of highly malignant potential[J]. Hum Pathol, 2015, 46(3):347-356. DOI: 10.1016/j.humpath.2014.11.018. doi:10.1016/j.humpath.2014.11.018 |
[19] | Nakada S, Minato H, Nojima T. Clinicopathological differences between variants of the NAB2-STAT6 fusion gene in solitary fibrous tumors of the meninges and extra-central nervous system[J]. Brain Tumor Pathol, 2016, 33(3):169-174. DOI: 10.1007/s10014-016-0264-6. doi:10.1007/s10014-016-0264-6 |
[20] | Chuang IC, Liao KC, Huang HY, et al. NAB2-STAT6 gene fusion and STAT6 immunoexpression in extrathoracic solitary fibrous tumors: the association between fusion variants and locations[J]. Pathol Int, 2016, 66(5):288-296. DOI: 10.1111/pin.12408. doi:10.1111/pin.12408pmid:27039712 |
[21] | 丁志燕, 王艳芬, 王璇, 等. 信号转导及转录激活因子6在孤立性纤维性肿瘤中的表达和意义[J]. 中华病理学杂志, 2017, 46(4):235-239. DOI: 10.3760/cma.j.issn.0529-5807.2017.04.004. doi:10.3760/cma.j.issn.0529-5807.2017.04.004 |
[22] | Barthelmeß S, Geddert H, Boltze C, et al. Solitary fibrous tumors/hemangiopericytomas with different variants of the NAB2-STAT6 gene fusion are characterized by specific histomorphology and distinct clinicopathological features[J]. Am J Pathol, 2014, 184(4):1209-1218. DOI: 10.1016/j.ajpath.2013.12.016. doi:S0002-9440(14)00021-2pmid:24513261 |
[23] | Nielsen GP, O'Connell JX, Dickersin GR, et al. Solitary fibrous tumor of soft tissue: a report of 15 cases, including 5 malignant examples with light microscopic, immunohistochemical, and ultrastructural data[J]. Mod Pathol, 1997, 10(10):1028-1037. |
[24] | Lahon B, Mercier O, Fadel E, et al. Solitary fibrous tumor of the pleura: outcomes of 157 complete resections in a single center[J]. Ann Thorac Surg, 2012, 94(2):394-400. DOI: 10.1016/j.athoracsur.2012.04.028. doi:10.1016/j.athoracsur.2012.04.028 |
[25] | Ito H, Arai T, Niino H, et al. Malignant recurrence of solitary fibrous tumor of the pleura developed 20 years after the surgery: a case report of re-extirpation[J]. Kyobu Geka, 1998, 51(6):504-507. |
[26] | England DM, Hochholzer L, McCarthy MJ. Localized benign and malignant fibrous tumors of the pleura. A clinicopathologic review of 223 cases[J]. Am J Surg Pathol, 1989, 13(8):640-658. DOI: 10.1097/00000478-198908000-00003. doi:10.1097/00000478-198908000-00003pmid:2665534 |
[27] | Magdeleinat P, Alifano M, Petino A, et al. Solitary fibrous tumors of the pleura: clinical characteristics, surgical treatment and outcome[J]. Eur J Cardiothorac Surg, 2002, 21(6):1087-1093. DOI: 10.1016/s1010-7940(02)00099-4. doi:10.1016/s1010-7940(02)00099-4 |
[28] | Lang N, Zhang E, Xing X, et al. Solitary fibrous tumour of the spine: imaging features of a commonly misdiagnosed entity[J]. Eur Radiol, 2018, 28(9):3986-3995. DOI: 10.1007/s00330-018-5349-7. doi:10.1007/s00330-018-5349-7 |
[29] | Murata K, Endo K, Aihara T, et al. Salvage carbon ion radiotherapy for recurrent solitary fibrous tumor: a case report and literature review[J]. J Orthop Surg (Hong Kong), 2020, 28(1):2309499019896099. DOI: 10.1177/2309499019896099. doi:10.1177/2309499019896099 |
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