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伴有MSMB-NCOA4融合及可能原位基底细胞癌的前列腺基底细胞癌:病例报告

Basal Cell Carcinoma of Prostate With MSMB-NCOA4 Fusion and a Probable Basal Cell Carcinoma In Situ: Case Report.

作者信息

Pedersen Vilde, Petersen Katrine S, Brasso Klaus, Østrup Olga, Loya Anand C

机构信息

Department of Pathology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark.

Department of Pathology, Zealand University Hospital, Roskilde, Denmark.

出版信息

Int J Surg Pathol. 2021 Dec;29(8):850-855. doi: 10.1177/10668969211017321. Epub 2021 May 12.

Abstract

Basal cell carcinomas of prostate (BCCP) are very rare. Most arise in the transition zone and thus are associated with lower urinary tract symptoms and rarely associated with elevated prostate-specific antigen (PSA). These features make diagnosis/early diagnosis difficult because of the routine protocols followed. Basal cell carcinomas have distinctive histopathological, immunohistochemical, and to some extent also different molecular characteristics. Basal cell carcinoma in situ (BCCIS) is a nonexistent histological lesion as per the current literature, but here is an attempt to describe it through this case.A 74-year-old man presented with hematuria and previous diagnosis of prostatic hyperplasia. Based on this history, he underwent a prostatectomy ad modum Freyer. Pathological examination surprisingly revealed a diffusely infiltrative tumor with nonacinar adenocarcinoma morphology and many glandular structures probably representing BCCIS. Tumor was diagnosed as BCCP. Patient presented with metastasis to the abdominal wall 8 months postprostatectomy.BCCP is an aggressive type of prostate cancer, which might be challenging to diagnose based on routine protocols. This results in delayed diagnosis and treatment and thus poor prognosis. Furthermore, patients with this subtype of prostate cancer need appropriately designed, and maybe a totally different follow-up regimen as PSA is of no use for BCCP patients. Finally, diagnosis of BCCIS, if agreed upon its existence needs to be studied in larger cohorts as a precursor lesion.

摘要

前列腺基底细胞癌(BCCP)非常罕见。大多数起源于移行带,因此与下尿路症状相关,很少与前列腺特异性抗原(PSA)升高相关。由于遵循常规方案,这些特征使得诊断/早期诊断变得困难。基底细胞癌具有独特的组织病理学、免疫组织化学特征,在一定程度上分子特征也有所不同。根据目前的文献,原位基底细胞癌(BCCIS)是不存在的组织学病变,但本文试图通过该病例对其进行描述。一名74岁男性因血尿就诊,既往诊断为前列腺增生。基于此病史,他接受了改良Freyer前列腺切除术。病理检查令人惊讶地发现了一种弥漫性浸润性肿瘤,具有非腺泡腺癌形态,许多腺管结构可能代表BCCIS。肿瘤被诊断为BCCP。患者在前列腺切除术后8个月出现腹壁转移。BCCP是一种侵袭性前列腺癌,基于常规方案可能难以诊断。这导致诊断和治疗延迟,预后不良。此外,这种前列腺癌亚型的患者需要设计适当的,可能完全不同的随访方案,因为PSA对BCCP患者无用。最后,如果认可BCCIS的存在,其诊断需要在更大的队列中作为前驱病变进行研究。

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