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前列腺炎症性肌纤维母细胞瘤一例报道并文献复习 被引量:3

Inflammatory myofibroblastic tumor of the prostate: a case report and review of the literatures
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摘要 目的探讨前列腺炎症性肌纤维母细胞瘤(IMT)的诊治方案。方法前列腺IMT是一种罕见的交界性肿瘤,其临床特点、影像学特征无特异性,诊断困难,主要依靠病理诊断。回顾性分析1例前列腺IMT患者的临床资料并复习相关文献。患者,男性,62岁,间歇性尿频、尿痛、排尿困难4年,加重1个月。CT提示前列腺囊性占位,两次行经尿道前列腺电切术(TURP),术后病理证实为前列腺炎症性肌纤维母细胞瘤。结果首次TURP术后两月前列腺炎症性肌纤维母细胞瘤复发,行二次TURP术后随访14个月,患者排尿正常,无复发和转移。结论前列腺IMT的诊断主要依靠病理,有复发可能,手术切除肿瘤是首选方法,术后随访,复查极为重要。 Objective To investigate the diagnosis and treatment of inflammatory myofibroblastic tumor (IMT) of the prostate. Methods Prostate IMT is a rare borderline tumor, of which clinical features, imaging features are non-speclfic, its diagnosis is difficult, and rely mainly on the pathological diagnosis. The clinical data of a case of IMT of the prostate were analyzed retrospectively and relevant literatures were reviewed. The patient, male, 62 years old, complained for intermittent frequency, adyuria and dysuria for 4 years, aggravating in month. CT prompted prostate cystic space-occupying. Two sequential TURP surgeries, pathologically confirmed as inflammatory myofibroblastic tumor of the prostate. Results Two months after the first TURP, the inflammatory myofibroblastic tumor of the prostate recurrence. Followed up for 14 months, the patient sustained normal micturition, without recurrence or metastasis after the second TURP. Conclusions The diagnosis of IMT of prostate relies on the pathologic, and the recurrence, surgical resection is the preferred method, and postoperative follow-up is extremely important.
出处 《中华腔镜泌尿外科杂志(电子版)》 2013年第6期45-47,共3页 Chinese Journal of Endourology(Electronic Edition)
关键词 炎症性肌纤维母细胞瘤 前列腺 Inflammatory myofibroblastic tumor Prostate
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  • 1王坚,朱雄增.软组织肿瘤病理学[M].北京:人民卫生出版社.2008:81-84,124-126.
  • 2Emerson R E, Cheng L. Immunohistoehemical markers in the evaluation of tumors of the urinary bladder: a review[J]. Anal Quant Cytol Histol, 2005, 27: 301.
  • 3Elizabeth A, Montgomery M D. Inflammatory Myofibroblastic Tumors of the Urinary Tract: A Clinicopathologic Study of 46 Cases, Including a Malignant Example Inflammatory Fihmsarcoma and a Subset Associated With High - grade Urothelial Carcinoma [J ]. The Journal of Urology, 2008, 180: 1235.
  • 4Sirvent N, Hawkins A L, Moeglin D, et al. ALK probe rear - rangement in a t ( 2 ; 11 ; 2 ) ( p23 ; p15 ; q31 ) translocation found in a prenatal myofibroblastie fibrous lesion; toward a molecular defini-tion of an inflammatory myofibroblastic tumor family[J]. Genes Chromosomes Cancer, 2001, 31 ( 1 ) : 85.
  • 5Sirvent N, Hawkins A L, Moeglin D, et al. ALK probe rear - rangement in a t ( 2 ; 11 ; 2 ) ( p23 ; p15 ; q31 ) translocation found in a prenatal myofibroblastie fibrous lesion; toward a molecular defini--tion of an inflammatory myofibroblastic tumor family[J]. Genes Chromosomes Cancer, 2001, 31 ( 1 ) : 85.
  • 6Maruya S, Kurotaki H, Hashimoto T, et al. Inflammatory pseudotumour(plasma cell granuloma arising in the maxillary sinus[J]. Acta Otolaryngol, 2005, 125(3): 322.
  • 7Harik L R, Merino C, Coindre J M, et al. Pseudosarcomatous myofibroblastic proliferations of the bladder: a clinicopathologic study of 42 cases[J]. Am J Surg Pathol, 2006, 30 : 787.
  • 8Lawrence B, Perez-Atayde A, Hibbard M K, et al. TPM3 - ALK and TPM4 - ALK oncogenes in inflammatory myofibroblastic tumors[J]. Am J Pathol, 2000, 157(2) : 377.
  • 9Coffin C M, Fletcher J A. Inflammatory myofibroblastic tumour/Fleteher C D, Unni K K, Merten F. World health organization classification of tumors: pathology and genetics of tumours of soft tissue and bone[M]. Lyon: IARC Press, 2002: 91.
  • 10Montgomery E A, Shuster D D, Burkart A L, et al. Inflammatory myofibroblastic tumors of the urinary tract: a ctinicopathologic study of 46 cases, including a malignant example inflammatory fibrosarcoma and a subset associated with high -grade carcinoma[J]. Am J Surg Pathol, 2006, 30(12): 1502.

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