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前列腺基底细胞癌:一种极其罕见的肿瘤。

Basaloid carcinoma of the prostate: an extremely rare tumor.

作者信息

Rodriguez-Carlin Arquimedes, Arellano Leonardo, López-Fontana Gaston, Bolufer Eduardo, Castillo Octavio A

机构信息

Service of Urology, Clinica Indisa, Faculty of Medicine, Universidad Andrés Bello, Chile.

出版信息

Arch Esp Urol. 2013 May;66(4):380-4.

Abstract

OBJECTIVE

The basaloid carcinoma of the prostate (BC) is a rare malignant neoplasm arising from the basal cells of prostatic ducts and acini. We report a case and review the literature.

METHODS

A 76-year-old man presented with symptoms of lower obstructive uropathy, the IPSS score was 29 and prostate specific antigen (PSA)of 0,924 ng /ml. Transurethral resection of prostate (TURP) was performed in September 2008, histopathological diagnosis was BC. In February 2009 laparoscopic radical prostatectomy was performed.

RESULTS

Histopathological examination revealed a BC with adenoid cystic growth pattern, perineural infiltration and focal involvement of the left seminal vesicle. Immunohistochemically, the cells were negative for PSA, stained and were strongly positive for specific monoclonal antibodies anti-cytokeratin 34βE12, p63 and BCL-2. The patient has 23 months of follow-up, with complete continence and no evidence of tumor recurrence.

CONCLUSIONS

The BC is an extremely rare subtype of malignant tumors of the prostate, where immunohistochemistry plays a fundamental role in diagnosis.

摘要

目的

前列腺基底细胞癌(BC)是一种起源于前列腺导管和腺泡基底细胞的罕见恶性肿瘤。我们报告一例病例并复习相关文献。

方法

一名76岁男性出现下尿路梗阻症状,国际前列腺症状评分(IPSS)为29分,前列腺特异性抗原(PSA)为0.924 ng/ml。2008年9月行经尿道前列腺切除术(TURP),组织病理学诊断为BC。2009年2月行腹腔镜前列腺癌根治术。

结果

组织病理学检查显示为具有腺样囊性生长模式、神经周围浸润及左侧精囊局部受累的BC。免疫组化显示,细胞PSA阴性,抗细胞角蛋白34βE12、p63和BCL-2特异性单克隆抗体染色呈强阳性。该患者随访23个月,尿控完全,无肿瘤复发迹象。

结论

BC是前列腺恶性肿瘤中极其罕见的亚型,免疫组化在其诊断中起重要作用。

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