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DOI 10.1177/15579883221143182

Медицинская библиотека · American journal of men's health · 2022

Sclerosing Adenosis of the Prostate-A Benign Lesion Similar to Prostate Cancer: A Case Report and Literature Review.

Yao Huibao, Tang Gonglin, Cui Yuanshan, Wu Jitao

ОбзорКлинический случайСтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Sclerosing adenosis of the prostate (SAP) is a rare benign non-neoplastic small acinar hyperplasia. Like sclerosing adenosis of the breast, which is confused with breast cancer, SAP is a trap in the pathological differential diagnosis of benign and malignant lesions of the prostate. We report such a case to help colleagues better distinguish and diagnose such diseases. A 75-year-old patient with SAP had a prostate specific antigen (PSA) level of 11.0 ng/mL, and he had been suffering from progressive dysuria for 3 years. The central glandular area and the right periphery of the prostate were found to have nodular low signals on magnetic resonance imaging (MRI). Prostate biopsy showed that basal cells were positive for P63 and P504s, few basal cells were positive for S-100, and the positive rate of Ki67 was approximately 2%. We consider that the possibility of SAP is high. The patient was treated conservatively and was discharged in good health, free of dysuria and other problems. SAP is a rare benign lesion that is easily misdiagnosed as prostate cancer. The prostatic gland tube has a complete basal cell layer surrounding it, as well as myoepithelial cell metaplasia of basal cells, which is a key trait in distinguishing it from prostate cancer. Although the latest research indicates that SAP does not require treatment, the question of whether it is a risk factor for prostate cancer remains unanswered.

Для цитирования: Yao Huibao, Tang Gonglin, Cui Yuanshan, Wu Jitao. Sclerosing Adenosis of the Prostate-A Benign Lesion Similar to Prostate Cancer: A Case Report and Literature Review.. American journal of men's health. 2022. DOI: 10.1177/15579883221143182.

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