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Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy

OBJECTIVE: Prostate cancer (PC) is one of the most common cancer and an important reason of cancer specific death. The incidence of patients who diagnosed at low stage increased because of widespread using Prostate Specific Antigen (PSA) testing. We evaluated the patients who were diagnosed single m...

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Autores principales: Çalışkan, Selahattin, Koca, Orhan, Akyüz, Mehmet, Öztürk, Metin, Karaman, Muhammet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asian Pacific Prostate Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685238/
https://www.ncbi.nlm.nih.gov/pubmed/26779460
http://dx.doi.org/10.1016/j.prnil.2015.09.003
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author Çalışkan, Selahattin
Koca, Orhan
Akyüz, Mehmet
Öztürk, Metin
Karaman, Muhammet
author_facet Çalışkan, Selahattin
Koca, Orhan
Akyüz, Mehmet
Öztürk, Metin
Karaman, Muhammet
author_sort Çalışkan, Selahattin
collection PubMed
description OBJECTIVE: Prostate cancer (PC) is one of the most common cancer and an important reason of cancer specific death. The incidence of patients who diagnosed at low stage increased because of widespread using Prostate Specific Antigen (PSA) testing. We evaluated the patients who were diagnosed single microscopic focus of adenocarcinoma and treated radical prostatectomy at final pathology. METHODS: The patients who underwent transrectal ultrasound guided prostate biopsy between January 2004 and January 2012 were enrolled retrospectively. We extracted the patients who were diagnosed single microscopic focus of adenocarcinoma and treated with RP. Single microscopic adenocarcinoma was defined as one single focus measuring 3 mm or less, well differentiated (Gleason ≤6) adenocarcinoma. 37 patients were included at the study. Clinical data; including age, serum PSA levels, PSA density and prior biopsy and prostatectomy specimen results were recorded. In pathological examination; high molecular weight cytokeratin (HMW-CK), p63, and alpha-methylacyl-CoA racemase (AMACR) were used for differential diagnosis. RESULTS: The patients' ages were between 42 and 77 with a mean age of 64.9 ± 7.57 years. Mean PSA levels and prostate volumes were 8.03 ± 5.21 ng/ml and 54 ± 25.51 cc. T0, T2a, T2c and T3a were reported in 2 patients, 17 patients, 17 patients and 1 patient after pathological evaluation. According to the Gleason grading system; 6 patients were 7 (3 + 4), one patient was 7 (4 + 3), one patient was 5 (3 + 2) and 27 patients were 6 (3 + 3). CONCLUSION: Small volume of cancer at prostate biopsy is not necessarily small cancer in radical prostatectomy. The treatment choice may be over or under treatment for some patients, so the patients must be informed when choosing the treatment.
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spelling pubmed-46852382016-01-15 Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy Çalışkan, Selahattin Koca, Orhan Akyüz, Mehmet Öztürk, Metin Karaman, Muhammet Prostate Int Original Article OBJECTIVE: Prostate cancer (PC) is one of the most common cancer and an important reason of cancer specific death. The incidence of patients who diagnosed at low stage increased because of widespread using Prostate Specific Antigen (PSA) testing. We evaluated the patients who were diagnosed single microscopic focus of adenocarcinoma and treated radical prostatectomy at final pathology. METHODS: The patients who underwent transrectal ultrasound guided prostate biopsy between January 2004 and January 2012 were enrolled retrospectively. We extracted the patients who were diagnosed single microscopic focus of adenocarcinoma and treated with RP. Single microscopic adenocarcinoma was defined as one single focus measuring 3 mm or less, well differentiated (Gleason ≤6) adenocarcinoma. 37 patients were included at the study. Clinical data; including age, serum PSA levels, PSA density and prior biopsy and prostatectomy specimen results were recorded. In pathological examination; high molecular weight cytokeratin (HMW-CK), p63, and alpha-methylacyl-CoA racemase (AMACR) were used for differential diagnosis. RESULTS: The patients' ages were between 42 and 77 with a mean age of 64.9 ± 7.57 years. Mean PSA levels and prostate volumes were 8.03 ± 5.21 ng/ml and 54 ± 25.51 cc. T0, T2a, T2c and T3a were reported in 2 patients, 17 patients, 17 patients and 1 patient after pathological evaluation. According to the Gleason grading system; 6 patients were 7 (3 + 4), one patient was 7 (4 + 3), one patient was 5 (3 + 2) and 27 patients were 6 (3 + 3). CONCLUSION: Small volume of cancer at prostate biopsy is not necessarily small cancer in radical prostatectomy. The treatment choice may be over or under treatment for some patients, so the patients must be informed when choosing the treatment. Asian Pacific Prostate Society 2015-12 2015-10-08 /pmc/articles/PMC4685238/ /pubmed/26779460 http://dx.doi.org/10.1016/j.prnil.2015.09.003 Text en Copyright © 2015 Asian Pacific Prostate Society, Published by Elsevier. All rights reserved. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Çalışkan, Selahattin
Koca, Orhan
Akyüz, Mehmet
Öztürk, Metin
Karaman, Muhammet
Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title_full Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title_fullStr Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title_full_unstemmed Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title_short Clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
title_sort clinical significance of single microscopic focus of adenocarcinoma at prostate biopsy
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685238/
https://www.ncbi.nlm.nih.gov/pubmed/26779460
http://dx.doi.org/10.1016/j.prnil.2015.09.003
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