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1.
Int Braz J Urol ; 40(4): 454-9; discussion 460-2, 2014.
Article in English | MEDLINE | ID: mdl-25251950

ABSTRACT

INTRODUCTION: Brachytherapy is an option for treating low-risk prostate cancer (PC). Biochemical control of low-risk disease can reach 95 %. The practice advocated is that a review of prostate biopsies should be mandatory before choosing the best treatment for patients with PC. Our objective was to evaluate the change in PC risk after review of a prostate biopsy by an experienced uropathologist at a reference hospital. MATERIALS AND METHODS: Between December 2003 and August 2012, 182 men were referred to our institution for brachytherapy to treat PC. Their slides were reviewed by the same uropathologist. RESULTS AND DISCUSSION: Classification risk disagreement occurred in 71 (39 %) cases, including one in which no tumor was observed. The main cause of risk change was related to the Gleason score (GS), with 57 (81.4 %) cases upgraded to GS 7 or 8. Tumor volume was also compared, although only the number of fragments was reported in most original reports. The concordance of the number of cores affected by tumor was 43.9 %, and in 49 % of the cases, the number was decreased by the uropathologist. Perineural invasion (PNI) was reported in one quarter of original reports, and the agrement was 58 %. CONCLUSION: Slide review by an uropathologist remains essential at reference radiotherapy centers for the treatment of PC. The change in PC risk evaluation is mainly due to the GS, but tumor volume and PNI, which are important for the characterization of tumor aggressiveness, are also misinterpreted and could drive a change in the therapy choice.


Subject(s)
Prostatic Neoplasms/pathology , Prostatic Neoplasms/radiotherapy , Risk Assessment/methods , Aged , Biopsy, Needle , Brachytherapy/methods , Humans , Male , Middle Aged , Neoplasm Grading , Neoplasm Staging , Observer Variation , Predictive Value of Tests , Prostate/pathology , Prostate-Specific Antigen/blood , Reference Values , Risk Factors , Tertiary Care Centers , Tumor Burden
2.
Int. braz. j. urol ; 40(4): 454-462, Jul-Aug/2014. tab, graf
Article in English | LILACS | ID: lil-723967

ABSTRACT

Introduction Brachytherapy is an option for treating low-risk prostate cancer (PC). Biochemical control of low-risk disease can reach 95%. The practice advocated is that a review of prostate biopsies should be mandatory before choosing the best treatment for patients with PC. Our objective was to evaluate the change in PC risk after review of a prostate biopsy by an experienced uropathologist at a reference hospital. Materials and Methods Between December 2003 and August 2012, 182 men were referred to our institution for brachytherapy to treat PC. Their slides were reviewed by the same uropathologist. Results and Discussion Classification risk disagreement occurred in 71 (39%) cases, including one in which no tumor was observed. The main cause of risk change was related to the Gleason score (GS), with 57 (81.4%) cases upgraded to GS 7 or 8. Tumor volume was also compared, although only the number of fragments was reported in most original reports. The concordance of the number of cores affected by tumor was 43.9%, and in 49% of the cases, the number was decreased by the uropathologist. Perineural invasion (PNI) was reported in one quarter of original reports, and the agreement was 58%. Conclusion Slide review by an uropathologist remains essential at reference radiotherapy centers for the treatment of PC. The change in PC risk evaluation is mainly due to the GS, but tumor volume and PNI, which are important for the characterization of tumor aggressiveness, are also misinterpreted and could drive a change in the therapy choice. .


Subject(s)
Aged , Humans , Male , Middle Aged , Prostatic Neoplasms/pathology , Prostatic Neoplasms/radiotherapy , Risk Assessment/methods , Biopsy, Needle , Brachytherapy/methods , Neoplasm Grading , Neoplasm Staging , Observer Variation , Predictive Value of Tests , Prostate-Specific Antigen/blood , Prostate/pathology , Reference Values , Risk Factors , Tertiary Care Centers , Tumor Burden
3.
Acta Cytol ; 48(2): 199-206, 2004.
Article in English | MEDLINE | ID: mdl-15085752

ABSTRACT

OBJECTIVE: To assess the rate of HER2/neu overexpression in cytologic specimens by immunocytochemistry (ICC) and compare these results in matched surgical specimens by immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH), when available. STUDY DESIGN: All cytologic specimens processed for HER2/neu evaluation by ICC (72 cases) and available corresponding histologic specimens (16 cases) were retrieved from our files. ICC was applied to previously Papanicolaou stained, routine fine needle aspirations specimens (64 cases) and cytocentrifuged, alcohol-fixed, fluid specimens (8 cases). FISH was performed on 6 histologic specimens. RESULTS: Overexpression of HER2/neu was seen in 7/22 breast cancers (31.8%), 3/18 pulmonary adenocarcinomas (16.6%), 2/5 colorectal adenocarcinomas (40%), 1/2 adenocarcinomas of the biliary system (50%), 1/3 thyroid papillary carcinomas (33.3%) and 1/3 prostate adenocarcinomas (33.3%). Sixteen cases had IHC in matched histologic specimens: 14 (87.5%) cases were concordant (11 negative and 3 positive in both specimens), 1 case was negative in the cytologic specimen and positive in the histologic specimen (with no amplification by FISH), and 1 case was positive in the cytologic specimen and negative in the histologic specimen (not informative by FISH). CONCLUSION: Our data suggest that overexpression of HER2/neu oncoprotein can be successfully detected in routine cytologic specimens, providing a simple, fast and cost-effective method of selecting patients for specific treatment.


Subject(s)
Biomarkers, Tumor/biosynthesis , Neoplasms/metabolism , Neoplasms/pathology , Receptor, ErbB-2/biosynthesis , Adenocarcinoma/metabolism , Adenocarcinoma/pathology , Biomarkers, Tumor/analysis , Carcinoma, Papillary/metabolism , Carcinoma, Papillary/pathology , Diagnosis, Differential , Female , Humans , Immunohistochemistry , In Situ Hybridization, Fluorescence , Male , Predictive Value of Tests , Receptor, ErbB-2/analysis , Reproducibility of Results , Up-Regulation/physiology
4.
Braz J Med Biol Res ; 34(7): 861-5, 2001 Jul.
Article in English | MEDLINE | ID: mdl-11449303

ABSTRACT

In addition to the mutations that underlie most cases of the multiple endocrine neoplasia type 1 (MEN1) syndrome, somatic mutations of the MEN1 gene have also been described in sporadic tumors like gastrinomas, insulinomas and bronchial carcinoid neoplasm. We examined exon 2 of this gene, where most of the mutations have been described, in 148 endocrine and nonendocrine sporadic tumors. DNA was obtained by phenol/chloroform extraction and ethanol precipitation from 92 formalin-fixed, paraffin-embedded samples, and from 40 fresh tumor tissue samples. We used 5 pairs of primers to encompass the complete coding sequence of exon 2 of the MEN1 gene that was screened by the polymerase chain reaction-single-stranded conformation polymorphism (PCR-SSCP) technique in 78 sporadic thyroid cancers: 28 follicular adenomas, 35 papillary carcinomas, 14 follicular carcinomas, and 1 anaplastic thyroid carcinoma. We also examined 46 adrenal lesions (3 hyperplasias, 3 adenomas and 35 adrenocortical carcinomas, 2 pheochromocytomas, 2 ganglioneuroblastomas, and 1 lymphoma) and 24 breast cancers (6 noninvasive, 16 infiltrating ductal, and 2 invasive lobular tumors). The PCR product of 5 tumors suspected to present band shifts by SSCP was cloned. Direct sense and antisense sequencing did not identify mutations. These results suggest that the MEN1 gene is not important in breast, thyroid or adrenal sporadic tumorigenesis. Because the frequency of mutations varies significantly among tumor subgroups and allelic deletions are frequently observed at 11q13 in thyroid and adrenal cancers, another tumor suppressor gene residing in this region is likely to be involved in the tumorigenesis of these neoplasms.


Subject(s)
Adrenal Gland Neoplasms/genetics , Breast Neoplasms/genetics , DNA, Neoplasm/analysis , Exons/genetics , Mutation/genetics , Neoplasm Proteins/genetics , Neoplasms/genetics , Proto-Oncogene Proteins , Adolescent , Adult , Aged , Child , Child, Preschool , DNA, Neoplasm/genetics , Female , Humans , Male , Middle Aged , Multiple Endocrine Neoplasia Type 1/genetics , Polymerase Chain Reaction , Polymorphism, Single-Stranded Conformational
5.
Braz. j. med. biol. res ; 34(7): 861-865, July 2001. ilus, tab
Article in English | LILACS | ID: lil-298670

ABSTRACT

In addition to the mutations that underlie most cases of the multiple endocrine neoplasia type 1 (MEN1) syndrome, somatic mutations of the MEN1 gene have also been described in sporadic tumors like gastrinomas, insulinomas and bronchial carcinoid neoplasm. We examined exon 2 of this gene, where most of the mutations have been described, in 148 endocrine and nonendocrine sporadic tumors. DNA was obtained by phenol/chloroform extraction and ethanol precipitation from 92 formalin-fixed, paraffin-embedded samples, and from 40 fresh tumor tissue samples. We used 5 pairs of primers to encompass the complete coding sequence of exon 2 of the MEN1 gene that was screened by the polymerase chain reaction-single-stranded conformation polymorphism (PCR-SSCP) technique in 78 sporadic thyroid cancers: 28 follicular adenomas, 35 papillary carcinomas, 14 follicular carcinomas, and 1 anaplastic thyroid carcinoma. We also examined 46 adrenal lesions (3 hyperplasias, 3 adenomas and 35 adrenocortical carcinomas, 2 pheochromocytomas, 2 ganglioneuroblastomas, and 1 lymphoma) and 24 breast cancers (6 noninvasive, 16 infiltrating ductal, and 2 invasive lobular tumors). The PCR product of 5 tumors suspected to present band shifts by SSCP was cloned. Direct sense and antisense sequencing did not identify mutations. These results suggest that the MEN1 gene is not important in breast, thyroid or adrenal sporadic tumorigenesis. Because the frequency of mutations varies significantly among tumor subgroups and allelic deletions are frequently observed at 11q13 in thyroid and adrenal cancers, another tumor suppressor gene residing in this region is likely to be involved in the tumorigenesis of these neoplasms


Subject(s)
Humans , Male , Female , Adrenal Gland Neoplasms/genetics , Breast Neoplasms/genetics , DNA, Neoplasm/analysis , Exons/genetics , Multiple Endocrine Neoplasia Type 1/genetics , Mutation/genetics , DNA, Neoplasm/genetics , Polymerase Chain Reaction , Polymorphism, Single-Stranded Conformational
6.
Mod Pathol ; 14(5): 428-36, 2001 May.
Article in English | MEDLINE | ID: mdl-11353053

ABSTRACT

Mutation of p53 is rare in localized prostate carcinoma. The oncoprotein MDM2, whose gene has a response element for p53, promotes the degradation of p53 protein and inhibits its transcriptional activation of genes related to cell cycle arrest and apoptosis, constituting a negative feedback control. We studied p53 and MDM2 expression by immunohistochemistry and looked for mutations in p53 exons 5 to 8 by polymerase chain reaction-single strand conformational polymorphism in 118 patients submitted to radical prostatectomy for localized prostate cancer. In 28 cases, we studied cell proliferation by immunohistochemistry, using antibody for Ki-67, and apoptosis by the deoxynucleotidyl transferase mediated dUTP biotin nick end labeling technique. Although no p53 mutations were found, p53 protein was detected in 31.4% of the cases, and these cases had higher Gleason scores (P = .03) and more advanced tumor stages (P = .02). MDM2 was overexpressed in 40.7% of the cases, and these cases had greater tumor volumes (P = .001). Tumors that were positive for both p53 and MDM2 were larger (P = .003) and of more advanced stage (P = .03). Within the 28-case subset, the proliferative index was higher among MDM2-positive tumors (P = .046), and the apoptotic index was lower among p53-positive tumors (P = .01). We conclude that, although p53 mutation is a rare event in prostate carcinogenesis, the detection of p53 protein by immunohistochemistry is common and is associated with decreased apoptosis and increased histologic grade and tumor stage. We also conclude that the overexpression of MDM2 has a role in prostate carcinogenesis, being frequently detected and associated with increased cell proliferation and tumor volume. Finally, we propose that the MDM2-positive/p53-positive phenotype identifies prostate cancers with aggressive behavior.


Subject(s)
Adenocarcinoma/metabolism , Neoplasm Proteins/metabolism , Nuclear Proteins , Prostatic Neoplasms/metabolism , Proto-Oncogene Proteins/metabolism , Adenocarcinoma/genetics , Adenocarcinoma/pathology , Adenocarcinoma/surgery , Aged , Apoptosis , Cell Division , DNA, Neoplasm/analysis , Genes, p53/genetics , Humans , In Situ Nick-End Labeling , Ki-67 Antigen/metabolism , Male , Middle Aged , Mutation , Neoplasm Proteins/genetics , Polymerase Chain Reaction , Polymorphism, Single-Stranded Conformational , Prostatic Neoplasms/genetics , Prostatic Neoplasms/pathology , Prostatic Neoplasms/surgery , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins c-mdm2 , Tumor Suppressor Protein p53/metabolism
7.
Eur Urol ; 38(6): 774-7, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11111200

ABSTRACT

OBJECTIVES: Lymphoma is the most frequent testicular malignancy in men over 60 years of age. Even though patients present initially with localized disease, the high incidence of bilateral involvement, synchronous or not, and early systemic dissemination are characteristic of these neoplasms. Sometimes the interval between tumor involvement of both testes is long. The question is raised whether either the patient has a predisposition to present new clones of transformed lymphocytes, or the same disease using the same pathway from a systemic reservoir infiltrates the contralateral testis. METHOD: Polymerase chain reaction and DNA sequencing were used to detect immunoglobulin heavy chain (IgH) rearrangement in paraffin-embedded specimens from asynchronous tumors affecting the right and left testis of a 85-year-old man with an interval period of 13 months. RESULTS: Both tumors showed the same IgH rearrangement. CONCLUSIONS: The lymphoma affecting the left and right testis derived from the same clone. It makes a strong case that lymphoma of the testis is the first manifestation of a systemic disease and should be treated aggressively early at the beginning of the disease.


Subject(s)
Lymphoma, Large B-Cell, Diffuse/genetics , Testicular Neoplasms/genetics , Aged , Aged, 80 and over , DNA, Neoplasm/chemistry , Humans , Immunoglobulin Heavy Chains/chemistry , Lymphoma, Large B-Cell, Diffuse/pathology , Male , Polymerase Chain Reaction , Testicular Neoplasms/pathology , Testis/pathology , Time Factors
8.
Arq Gastroenterol ; 37(4): 197-202, 2000.
Article in Portuguese | MEDLINE | ID: mdl-11460599

ABSTRACT

Little change was observed in the histological criteria of reflux esophagitis since the studies of Ismail-Beiji, Pope (1970) and Weinstein (1975). The 24-hour esophageal pHmetry has been proposed as a high sensitivity method in diagnosis of gastroesophageal reflux disease patients. In this study we selected 35 patients with histological esophagitis and submitted them to 24-hour esophageal pHmetry. We determined histological differences according to reflux pattern, endoscopic esophagitis grades and age. The sensitivity of 24-hour esophageal pHmetry was 60.0% in our patients. There are higher histological alterations in patients with more severe patterns of reflux (supine and combined) and significant difference (P < 0.05) in observed quantitative exocytosis between moderate and severe endoscopic esophagitis. There are no difference between histological esophagitis criteria and age groups.


Subject(s)
Esophagitis, Peptic/pathology , Gastroesophageal Reflux/pathology , Adolescent , Adult , Age Factors , Aged , Child , Esophagus/chemistry , Female , Humans , Hydrogen-Ion Concentration , Male , Middle Aged , Monitoring, Ambulatory , Prospective Studies , Sensitivity and Specificity , Severity of Illness Index
9.
Head Neck ; 21(7): 602-5, 1999 Oct.
Article in English | MEDLINE | ID: mdl-10487946

ABSTRACT

BACKGROUND: The MACIS score uses metastasis, age, completeness of resection, local invasion, and tumor size to stratify patients with papillary thyroid carcinoma (PTC) into four groups with different survival. METHODS: Immunostaining for proliferating cell nuclear antigen (PCNA) was done in 43 cases of PTC. Relationships between proliferative index (percentage of cells that were PCNA positive) and the MACIS parameters were examined. Double staining for PCNA and for silver-stained nucleolar organizer regions (AgNORs, indicating proliferation) was performed in 10 cases. RESULTS: PCNA was detected only in tumor cells. The proliferative index was low (mean, 14.2%; median, 13.0%), did not differ between MACIS groups (p = 0.56), and showed no association with individual MACIS parameters. PCNA immunostaining correlated with AgNOR staining. The mean AgNOR count was 2.28 in PCNA-positive cells and 1.85 in PCNA-negative cells (p

Subject(s)
Carcinoma, Papillary/pathology , Nucleolus Organizer Region/pathology , Proliferating Cell Nuclear Antigen/analysis , Thyroid Neoplasms/pathology , Adult , Aged , Biopsy, Needle , Carcinoma, Papillary/diagnosis , Carcinoma, Papillary/secondary , Carcinoma, Papillary/surgery , Female , Humans , Immunohistochemistry , Lymphatic Metastasis , Male , Middle Aged , Neoplasm Invasiveness , Predictive Value of Tests , Sensitivity and Specificity , Thyroid Neoplasms/diagnosis , Thyroid Neoplasms/surgery
10.
Braz J Med Biol Res ; 32(3): 283-8, 1999 Mar.
Article in English | MEDLINE | ID: mdl-10347785

ABSTRACT

The surgical specimens from 51 men submitted to radical prostatectomy for localized prostate cancer were examined by immunohistochemistry using proliferation cell nuclear antigen (PCNA) monoclonal antibody to evaluate the proliferative index (PI). The relationship between PI, biological variables and p53 protein expression was evaluated by immunohistochemistry. PI was low in invasive localized prostate carcinoma (mean, 12.4%) and the incidence of PCNA-positive cells was significantly higher in tumors with p53 expression (P = 0.0226). There was no statistical difference in PCNA values when biological parameters such as Gleason score, tumor volume, extraprostatic involvement, seminal vesicle infiltration or lymph node metastasis were considered. We conclude that proliferative activity is usually low in prostate carcinoma but is correlated with p53 immune staining, indicating that p53 is important in cell cycle control in this neoplasm.


Subject(s)
Carcinoma/pathology , Gene Expression Regulation, Neoplastic/genetics , Genes, p53/genetics , Proliferating Cell Nuclear Antigen/analysis , Prostatic Neoplasms/pathology , Aged , Carcinoma/genetics , Cell Division , Humans , Male , Middle Aged , Neoplasm Staging , Prostatic Neoplasms/genetics
11.
Braz. j. med. biol. res ; 32(3): 283-8, Mar. 1999.
Article in English | LILACS | ID: lil-230454

ABSTRACT

The surgical specimens from 51 men submitted to radical prostatectomy for localized prostate cancer were examined by immunohistochemistry using proliferation cell nuclear antigen (PCNA) monoclonal antibody to evaluate the proliferative index (PI). The relationship between PI, biological variables and p53 protein expression was evaluated by immunohistochemistry. PI was low in invasive localized prostate carcinoma (mean, 12.4percent) and the incidence of PCNA-positive cells was significantly higher in tumors with p53 expression (P = 0.0226). There was no statistical difference in PCNA values when biological parameters such as Gleason score, tumor volume, extraprostatic involvement, seminal vesicle infiltration or lymph node metastasis were considered. We conclude that proliferative activity is usually low in prostate carcinoma but is correlated with p53 immune staining, indicating that p53 is important in cell cycle control in this neoplasm


Subject(s)
Humans , Male , Middle Aged , Carcinoma/pathology , Proliferating Cell Nuclear Antigen , Prostatic Neoplasms/pathology , Antibodies, Monoclonal , Genes, p53 , Immunohistochemistry , Neoplasm Staging
12.
Arq Gastroenterol ; 34(3): 169-74, 1997.
Article in English | MEDLINE | ID: mdl-9611295

ABSTRACT

A case of synchronous concurrent carcinoma and primary malignant lymphoma developing as two independent tumors of the stomach is presented. The clinical and pathological diagnosis and therapeutic problems associated with synchronous tumors of the stomach are discussed. A possible relationship between the two tumors and the role of Helicobacter pylori are also reviewed.


Subject(s)
Carcinoma/pathology , Lymphoma/pathology , Neoplasms, Multiple Primary/pathology , Stomach Neoplasms/pathology , Aged , Carcinoma/surgery , Female , Humans , Lymphoma/surgery , Neoplasms, Multiple Primary/surgery , Stomach Neoplasms/surgery
13.
Arq Gastroenterol ; 26(4): 105-10, 1989.
Article in Portuguese | MEDLINE | ID: mdl-2518589

ABSTRACT

This case was of a 45 year old female patient with a post-transfusion non-A non-B hepatitis which was accompanied since an acute phase to hepatic cirrhosis during a period of 159.7 months or 13.3 years. Four hepatic biopsies were carried out and they divided the follow-up into 5 evolutive periods. The biopsies revealed a progressive histologic from chronic persistent hepatitis to an active chronic hepatitis and cirrhosis. The aminotransferases followed a floating course in the whole period, with ALT greater than AST starting from the 3rd period. The 3rd period (from 5th to 8th year) was of least activity of the aminotransferases, and the 4th and 5th periods (from 8th to 13th year) showed the highest activity of ALT. The 2nd period (from 3rd to 5th year) showed the least portion of gamma globulin and the highest of albumin in comparison with the others. There was no connection between the levels of aminotransferases and the values of gamma globulin and albumin in the follow up process. The treatment employed in the 5th evolutive period (prednisone and colchicine) did not present any biochemical improvement.


Subject(s)
Hepatitis C/blood , Hepatitis C/pathology , Hepatitis, Chronic/blood , Hepatitis, Chronic/pathology , Liver Cirrhosis/blood , Liver Cirrhosis/pathology , Acute Disease , Alanine Transaminase/blood , Aspartate Aminotransferases/blood , Colchicine/therapeutic use , Female , Follow-Up Studies , Humans , Middle Aged , Prednisone/therapeutic use , Time Factors , Transfusion Reaction
15.
Arq Gastroenterol ; 19(2): 77-80, 1982.
Article in Portuguese | MEDLINE | ID: mdl-6764357

ABSTRACT

A case of one patient with hepatosplenic Schistosomiasis mansoni in association with histiocytic lymphoma is presented. The authors discuss the concomitance of the two pathologic processes, by comparing with other cases of the literature and speculating about its significance, there is the possibility of the schistosomiasis being related as the causing factor of the malignant disease.


Subject(s)
Lymphoma, Large B-Cell, Diffuse/complications , Schistosomiasis/complications , Splenic Neoplasms/complications , Adult , Humans , Liver/pathology , Lymphoma, Large B-Cell, Diffuse/pathology , Male , Schistosoma mansoni , Splenic Neoplasms/pathology
16.
Arq. gastroenterol ; 19(2): 77-80, 1982.
Article in Portuguese | LILACS | ID: lil-7083

ABSTRACT

Apresenta-se um caso de paciente portador de esquistossomose mansonica hepatoesplenica e linfoma histiocitico. Comenta-se a concomitancia dos dois processos patologicos, confrontando-se com outros casos da literatura e especulando-se sobre seu significado, havendo a possibilidade da esquistossomose ser relacionada como fator causal da doenca maligna


Subject(s)
Lymphatic Diseases , Lymphoma , Schistosomiasis , Liver Diseases, Parasitic , Splenic Diseases
18.
J Surg Oncol ; 13(3): 215-22, 1980.
Article in English | MEDLINE | ID: mdl-6990113

ABSTRACT

The case of a 26-year-old male with malignant carcinoid of the gallbladder is presented. Extensive review of the literature reveals this patient to be the third case of a metastasizing gall bladder carcinoid and the twelfth reported case in the literature.


Subject(s)
Carcinoid Tumor , Gallbladder Neoplasms , Adult , Carcinoid Tumor/pathology , Cholestasis/etiology , Gallbladder Neoplasms/pathology , Humans , Liver Neoplasms/pathology , Liver Neoplasms/secondary , Male
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