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1.
J Gastrointest Surg ; 16(8): 1573-80, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22618518

ABSTRACT

BACKGROUND: Current guidelines recommend the assessment of at least 12 lymph nodes for rectal cancer staging. Preoperative chemoradiotherapy may affect lymph node yield in this malignancy. This study investigated the impact of neoadjuvant chemoradiotherapy on the number of lymph nodes retrieved from rectal cancer patients. METHODS: An analysis of 162 rectal cancer patients who underwent curative surgery between 2005 and 2010. Seventy-one patients with stage II or III tumors received preoperative chemoradiotherapy. Using multivariate analysis, we assessed the correlation between clinicopathologic variables and number of retrieved lymph nodes. We also evaluated the association between survival and number of lymph nodes obtained. RESULTS: On multivariate analysis, preoperative chemoradiotherapy was the only variable to independently affect the number of lymph nodes obtained. The mean number of lymph nodes was 14.2 in patients treated with preoperative chemoradiotherapy and 19.4 in those not treated (P < 0.001). In the chemoradiotherapy group, 29.6 % of patients had fewer than 12 lymph nodes obtained compared with 9.9 % in the primary surgery group (P = 0.003). After chemoradiation, the number of retrieved lymph nodes was inversely correlated with tumor regression grade. Results showed that 5-year overall and disease-free survival were similar whether the patient had 12 or more nodes retrieved or not. CONCLUSIONS: Preoperative chemoradiotherapy reduces the lymph node yield in rectal cancer. The number of retrieved lymph nodes is affected by degree of histopathologic response of the tumor to chemoradiation. Thus, number of lymph nodes should not be used as a surrogate for oncologic adequacy of resection after neoadjuvant chemoradiotherapy for rectal cancer.


Subject(s)
Adenocarcinoma/therapy , Chemoradiotherapy, Adjuvant , Lymph Node Excision/statistics & numerical data , Neoadjuvant Therapy , Rectal Neoplasms/therapy , Rectum/surgery , Adenocarcinoma/mortality , Adenocarcinoma/pathology , Adult , Aged , Aged, 80 and over , Antimetabolites, Antineoplastic/therapeutic use , Female , Fluorouracil/therapeutic use , Humans , Male , Middle Aged , Multivariate Analysis , Neoplasm Staging , Rectal Neoplasms/mortality , Rectal Neoplasms/pathology , Retrospective Studies , Survival Analysis , Treatment Outcome
2.
Hum Immunol ; 71(3): 293-7, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20036705

ABSTRACT

Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory diseases of the bowel, of unknown origin. Exposure to specific environmental factors by genetically susceptible individuals, leading to an inadequate response of the immune system, is one of the potential explanations for the occurrence of these diseases. Natural killer cells are part of the innate immune system recognizing class I HLA (human leukocyte antigen) molecules on target cells through their membrane receptors. The main receptors of the natural killer cells are the killer immunoglobulinlike receptors (KIRs). Our study aimed to evaluate the association between the KIR genes in patients with inflammatory bowel diseases and healthy controls. We typed 15 KIR genes and HLA class I ligands in 248 unrelated Brazilian Caucasians, of which 111 had UC and 137 had CD, and 250 healthy controls by polymerase chain reaction using sequence-specific oligonucleotides and sequence-specific primers. We found an increase in KIR2DL2 in controls (inflammatory bowel disease [IBD]: p < 0.001; UC: p = 0.01; CD: p = not significant [NS]). The genotype 2DL2+/HLA-C lys(80)+ was also more common in controls (IBD: p = 0.005; UC: p = 0.01; CD: p = NS); as well as 2DL1+/HLA-C Asn(80)+ (IBD: p = 0.026; UC: p = NS;CD: p = NS). The imbalance between activating and inhibitory KIR and HLA ligands may explain, at least in part, the pathogenesis of these inflammatory bowel diseases.


Subject(s)
Colitis, Ulcerative/genetics , Crohn Disease/genetics , Genes, MHC Class I/genetics , Receptors, KIR/genetics , Adult , Brazil , Colitis, Ulcerative/epidemiology , Crohn Disease/epidemiology , Female , Humans , Male , White People
3.
Dig Dis Sci ; 55(8): 2203-10, 2010 Aug.
Article in English | MEDLINE | ID: mdl-19894117

ABSTRACT

BACKGROUND: RC-3095, a synthetic gastrin-releasing peptide (GRP) antagonist, has been identified as a candidate compound for the treatment of tumor necrosis factor (TNF)-dependent chronic inflammatory conditions. AIM: The aim of this study was to evaluate the effects of RC-3095 in a rat model of ulcerative colitis. METHODS: Ninety Wistar rats were included in the study. Colitis was induced by a single intracolonic application of acetic acid. Rats were divided into three groups of treatment: subcutaneous RC-3095, intracolonic mesalazine, and subcutaneous dexamethasone. Additionally, there was a fourth group of animals submitted to induction of colitis without receiving any form of treatment, and a fifth group in which no colitis was induced. Seventy-two hours after instillation of acetic acid, the animals were killed and the following parameters were assessed: morphological score of damage, histological score of colonic inflammation, and immunohistochemical expression of TNF-alpha and interleukin (IL)-1beta. RESULTS: RC-3095 was the only treatment to significantly reduce macroscopic and microscopic scores of inflammation as compared with the animals from the non-treated colitis group. RC-3095 also significantly reduced the colonic expression of TNF-alpha, but not the expression of IL-1beta. CONCLUSIONS: RC-3095 reduced the colitis severity in a well-established experimental model of IBD. The anti-inflammatory activity of this compound was associated with a reduction in the colonic expression of TNF-alpha. These results suggest that interference with GRP pathway might represent a potential new strategy for the treatment of ulcerative colitis that deserves further investigational studies.


Subject(s)
Bombesin/analogs & derivatives , Colitis, Ulcerative/drug therapy , Peptide Fragments/pharmacology , Animals , Bombesin/pharmacology , Colitis, Ulcerative/chemically induced , Colitis, Ulcerative/pathology , Colon/pathology , Female , Gastrin-Releasing Peptide/antagonists & inhibitors , Immunohistochemistry , Male , Rats , Rats, Wistar
4.
Arq. gastroenterol ; 46(4): 300-303, out.-dez. 2009. ilus
Article in English | LILACS | ID: lil-539625

ABSTRACT

Context: Management of complex anal fistulas is associated with the risk of sphincter injury and fecal incontinence. In recent years, fibrin glue has emerged as an alternative sphincter-preserving treatment for anal fistulas. To date, however, there is no consensus about the efficacy of the method. Objective: To specifically evaluate the fibrin glue injection in the management of complex cryptoglandular anal fistulas. Methods: We studied a series of patients with complex anal fistulas treated with fibrin glue between January 2005 and January 2007. Only patients with fistulas of cryptoglandular origin were analyzed. Patients with fistulas related to Crohn's disease, HIV or previous surgery were excluded from the study. Under spinal anesthesia, the fistulas were curetted and injected with fibrin glue. After treatment, patients were followed-up for 12 months. Results: Thirty-two patients were enrolled in the study. Two patients were lost to follow-up and were excluded. Out of the remaining 30 patients, only three healed successfully (10 percent). Among the 27 patients who failed to heal, 9 (33.3 percent) were diagnosed within the first postoperative month. In 13 patients (48.1 percent) the failure of treatment occurred in the period between 1 and 3 months, in 3 patients (11.1 percent) between 3 and 6 months, and in 2 patients (7.4 percent) between 6 and 9 months after surgery. No treatment-related complications were observed. Conclusions: In this series, fibrin glue treatment for complex cryptoglandular anal fistulas achieved a very low healing rate. Our results do not support the use of fibrin glue as a first-line treatment for patients with this type of fistula.


Contexto: O manejo das fistulas anais complexas está associado ao risco de lesão esfincteriana e incontinência fecal. Recentemente, a cola de fibrina surgiu como uma alternativa de tratamento conservador de esfíncter para as fístulas anais, porém até o momento não se chegou a um consenso quanto à eficácia do método. Objetivo: Avaliar o uso da cola de fibrina especificamente no tratamento de fístulas anais complexas de origem criptoglandular. Métodos: Foram estudados pacientes com fístulas anais complexas tratados com cola de fibrina entre janeiro de 2005 e janeiro de 2008. Somente pacientes com fístulas de origem criptoglandular foram analisados, sendo excluídos pacientes com fístulas relacionadas à doença de Crohn, ao HIV ou à cirurgia prévia. Sob anestesia espinhal, as fistulas eram curetadas, sendo após preenchidas com cola de fibrina. Depois do tratamento, os pacientes eram acompanhados por 12 meses. Resultados: Trinta e dois pacientes foram incluídos no estudo. Dois pacientes foram perdidos durante o seguimento pós-operatório, sendo excluídos. Dos 30 pacientes remanescentes, apenas 3 tiveram suas fistulas cicatrizadas (10 por cento). Com relação aos 27 pacientes nos quais não houve cicatrização, em 9 pacientes (33,3 por cento) a falha do tratamento foi diagnosticado nos primeiros 30 dias após a cirurgia, em 13 (48,8 por cento) entre 1 e 3 meses, em 3 (11,1 por cento) entre 3 e 6 meses e em 2 pacientes (7,4 por cento) entre 6 e 9 meses após a cirurgia. Não foram observadas complicações relacionadas ao tratamento. Conclusões: Nesta série, o tratamento das fístulas anais complexas de origem criptoglandular com cola de fibrina atingiu um índice muito baixo de cicatrização. Estes resultados não permitem a indicação da cola de fibrina como tratamento de primeira escolha para pacientes com esse tipo de fístula.


Subject(s)
Adult , Female , Humans , Male , Middle Aged , Young Adult , Fibrin Tissue Adhesive/therapeutic use , Rectal Fistula/therapy , Tissue Adhesives/therapeutic use , Follow-Up Studies , Prospective Studies , Treatment Failure , Young Adult
5.
World J Gastroenterol ; 15(36): 4566-70, 2009 Sep 28.
Article in English | MEDLINE | ID: mdl-19777616

ABSTRACT

AIM: To investigate the potential role of p53 codon 72 polymorphism as a risk factor for development of anal cancer. METHODS: Thirty-two patients with invasive anal carcinoma and 103 healthy blood donors were included in the study. p53 codon 72 polymorphism was analyzed in blood samples through polymerase chain reaction-restriction fragment length polymorphism and DNA sequencing. RESULTS: The relative frequency of each allele was 0.60 for Arg and 0.40 for Pro in patients with anal cancer, and 0.61 for Arg and 0.39 for Pro in normal controls. No significant differences in distribution of the codon 72 genotypes between patients and controls were found. CONCLUSION: These results do not support a role for the p53 codon 72 polymorphism in anal carcinogenesis.


Subject(s)
Anus Neoplasms/genetics , Genes, p53 , Adult , Aged , Aged, 80 and over , Anus Neoplasms/epidemiology , Codon , Female , Gene Frequency , Humans , Male , Middle Aged , Polymerase Chain Reaction , Polymorphism, Genetic , Risk Factors , Statistics as Topic
6.
Arq Gastroenterol ; 46(4): 300-3, 2009.
Article in English | MEDLINE | ID: mdl-20232010

ABSTRACT

CONTEXT: Management of complex anal fistulas is associated with the risk of sphincter injury and fecal incontinence. In recent years, fibrin glue has emerged as an alternative sphincter-preserving treatment for anal fistulas. To date, however, there is no consensus about the efficacy of the method. OBJECTIVE: To specifically evaluate the fibrin glue injection in the management of complex cryptoglandular anal fistulas. METHODS: We studied a series of patients with complex anal fistulas treated with fibrin glue between January 2005 and January 2007. Only patients with fistulas of cryptoglandular origin were analyzed. Patients with fistulas related to Crohn's disease, HIV or previous surgery were excluded from the study. Under spinal anesthesia, the fistulas were curetted and injected with fibrin glue. After treatment, patients were followed-up for 12 months. RESULTS: Thirty-two patients were enrolled in the study. Two patients were lost to follow-up and were excluded. Out of the remaining 30 patients, only three healed successfully (10%). Among the 27 patients who failed to heal, 9 (33.3%) were diagnosed within the first postoperative month. In 13 patients (48.1%) the failure of treatment occurred in the period between 1 and 3 months, in 3 patients (11.1%) between 3 and 6 months, and in 2 patients (7.4%) between 6 and 9 months after surgery. No treatment-related complications were observed. CONCLUSIONS: In this series, fibrin glue treatment for complex cryptoglandular anal fistulas achieved a very low healing rate. Our results do not support the use of fibrin glue as a first-line treatment for patients with this type of fistula.


Subject(s)
Fibrin Tissue Adhesive/therapeutic use , Rectal Fistula/therapy , Tissue Adhesives/therapeutic use , Adult , Female , Follow-Up Studies , Humans , Male , Middle Aged , Prospective Studies , Treatment Failure , Young Adult
7.
Rev. bras. colo-proctol ; 27(3): 330-332, jul.-set. 2007. ilus
Article in Portuguese | LILACS | ID: lil-471022

ABSTRACT

O Carcinoma basocelular (CBC) é a mais freqüente das neoplasias epiteliais, localizando-se preferencialmente em áreas expostas ao sol. A ocorrência deste tumor na região perianal é extremamente rara. Neste artigo, relatamos um caso de CBC perianal. Apresentamos também uma revisão da literatura médica sobre o tema, salientando as características clínicas e histopatológicas, bem como o tratamento preconizado para esse tipo de tumor.


Basal Cell Carcinoma (BCC) is the most common skin cancer. It is preferentially found in sun-exposed areas and it is extremely rare at perianal region. In this article, we report a case of perianal BCC. In addition, we present a review of the medical literature on this subject, outlining clinical and histologic characteristics of this type of tumor as well as the choices of treatment.


Subject(s)
Humans , Anal Canal , Anus Neoplasms , Carcinoma, Basal Cell , Skin Neoplasms
8.
Anal Quant Cytol Histol ; 25(4): 215-20, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12961828

ABSTRACT

OBJECTIVE: To investigate the prognostic value of nuclear features in rectal carcinoma. STUDY DESIGN: High-resolution imagery of 3,635 nuclei from 51 patients operated on for rectal cancer at various Dukes' stages was digitally recorded. A set of 93 features descriptive of the spatial and statistical distribution of nuclear chromatin was computed for each nucleus to derive a digital signature. Karyometric features were analyzed for correlation with progression of disease and death. RESULTS: Multivariate analysis of main karyometric features in comparison with cancer staging demonstrated that total optical density and clumpness, as well as average nuclear signature, had significant prognostic value in predicting cancer-related death. CONCLUSION: Digital signature seems to have a role as prognostic factor in rectal cancer. The method could be a useful parameter in deciding whether to perform adjuvant therapy in particular subgroups of patients, independently of tumor staging. However, these observations need to be substantiated with additional studies, including larger numbers of patients.


Subject(s)
Carcinoma/ultrastructure , Chromatin/ultrastructure , Cytogenetic Analysis/methods , Rectal Neoplasms/ultrastructure , Adult , Aged , Carcinoma/mortality , Female , Humans , Male , Middle Aged , Prognosis , Rectal Neoplasms/mortality , Survival Analysis
9.
Dis Colon Rectum ; 46(8): 1032-7, 2003 Aug.
Article in English | MEDLINE | ID: mdl-12907896

ABSTRACT

PURPOSE: This study was conducted to assess the feasibility of the sentinel lymph node procedure in patients with epidermoid carcinoma of the anal canal. METHODS: Between February 2001 and November 2002, 14 patients with epidermoid carcinoma of the anal canal and no clinical evidence of inguinal involvement were prospectively enrolled in the study. The sentinel lymph node procedure consisted of a combination of preoperative lymphoscintigraphy with technetium 99m dextran 500 injected around the tumor and intraoperative detection of the sentinel node with a gamma probe. Patent blue V dye was also injected at the periphery of the tumor to facilitate direct identification of the blue-stained lymph node. After removal, the sentinel node was studied by hematoxylin and eosin staining and immunohistochemistry for pancytokeratins (antigen A1 and A3). RESULTS: Detection and removal of sentinel lymph nodes was possible in all patients. There was no correlation between tumor size and pattern of lymphatic drainage to the groin. Tumors located in the midline of the anal canal gave rise to bilateral sentinel nodes in eight of nine cases. In total, 23 sentinel lymph nodes were removed. One patient (7.1 percent) had a node identified as positive for metastatic carcinoma on immunohistochemical staining. Surgical complications were minimal. CONCLUSIONS: The standardized technique was safe and highly effective in sampling inguinal sentinel lymph nodes in carcinoma of the anal canal. It also proved to be useful as an instrument to detect micrometastatic deposits in clinically normal nodes. Our early results suggest the sentinel lymph node procedure may have a role in guiding a more selective approach for patients with anal cancer. Additional studies in a larger patient population to determine the sensitivity and specificity of this method are warranted.


Subject(s)
Anus Neoplasms/pathology , Carcinoma, Squamous Cell/pathology , Sentinel Lymph Node Biopsy/methods , Aged , Antigens, Neoplasm/analysis , Anus Neoplasms/diagnostic imaging , Carcinoma, Squamous Cell/diagnostic imaging , Feasibility Studies , Female , Humans , Immunohistochemistry , Keratins/analysis , Male , Middle Aged , Prospective Studies , Radionuclide Imaging
10.
Anal Quant Cytol Histol ; 25(1): 25-30, 2003 Feb.
Article in English | MEDLINE | ID: mdl-12630079

ABSTRACT

OBJECTIVE: To characterize, by morphometric and chromatin texture analysis, a series of rectal carcinomas classified according to Dukes staging. STUDY DESIGN: High-resolution imagery of 6,001 nuclei from 51 specimens of rectal carcinoma and 22 specimens of normal rectal tissue was digitally recorded. A set of 93 features descriptive of the spatial and statistical distribution of nuclear chromatin was computed for each nucleus to form a characteristic signature. RESULTS: Rectal carcinomas were significantly different from normal rectum in their digital signature. Eleven karyometric features, such as nuclear area and total optical density, were clearly different between the groups, with significant differences found in analysis of 8 of those features. The most distinctive pattern in lesion signatures in comparison with normal rectal tissue was observed at Dukes' stage D. However, the highest average signature values were seen at Dukes' stage B. The lesion signatures and total optical density observed in cancer specimens deviated markedly from values in the normal group. CONCLUSION: Chromatin texture signature proved to be a useful method of identifying and characterizing nuclear differences between rectal carcinoma and normal rectal tissue.


Subject(s)
Adenocarcinoma/pathology , Cell Nucleus/pathology , Chromatin/pathology , Rectal Neoplasms/pathology , Rectum/pathology , Adenocarcinoma/classification , Cell Nucleus/classification , Humans , Image Processing, Computer-Assisted , Neoplasm Staging , Rectal Neoplasms/classification , Rectum/anatomy & histology
11.
Int J Colorectal Dis ; 17(5): 359-61, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12420731

ABSTRACT

BACKGROUND AND AIMS: Metastatic spread of a distant tumor to the rectum is extremely rare. To our knowledge, there have been no published reports of hematogenic metastasis from a renal cell carcinoma to the rectum. PATIENTS AND METHODS: A patient with a renal cell carcinoma was initially treated by a radical right nephrectomy. RESULTS: Nine months after the surgery he started to have multiple episodes of hematochezia. Colonoscopy showed a nodular lesion located in the distal rectum, and biopsy revealed an undifferentiated carcinoma. The patient then underwent abdominoperineal resection of the rectum, and histological examination showed metastatic renal clear cell carcinoma. CONCLUSION: This case represents an exceedingly rare condition, which has never been reported before.


Subject(s)
Carcinoma, Renal Cell/secondary , Kidney Neoplasms/pathology , Rectal Neoplasms/secondary , Humans , Male , Middle Aged , Tomography, X-Ray Computed
12.
Int J Colorectal Dis ; 17(1): 42-5, 2002 Jan.
Article in English | MEDLINE | ID: mdl-12018453

ABSTRACT

BACKGROUND AND AIM: Von Willebrand factor (vWF) is a protein that mediates adherence of platelets to subendothelium during primary hemostasis. High vWF plasma concentrations have been reported in patients with various types of cancer, such as squamous cell carcinoma of the larynx and the cervix. This effect is associated with tumor-related angiogenesis and the metastatic process. The aim of this study was to determine plasma levels of vWF in a series of patients with colorectal carcinoma and the correlation of these values with specific prognostic predictors for the disease. PATIENTS AND METHODS: vWF was measured by quantitative immunoelectrophoresis in 75 patients with colorectal carcinoma at various Dukes' stages and compared with results from 88 healthy controls. RESULTS: Cancer patients had significantly higher vWF concentrations than controls. vWF plasma levels were associated with tumor staging, invasion of adjacent organs by the tumor, and presence of distant metastases. There was no significant correlation between vWF values and tumor size, histological grading, or plasma carcinoembryonic antigen levels. CONCLUSIONS: The levels of vWF are elevated in patients with colorectal cancer, and these values tend to increase with tumor progression. Considering that vWF is related to the process of tumor angiogenesis and may contribute to metastatic dissemination of malignant cells, further studies of its potential role as a marker of tumor progression in patients with colorectal cancer are warranted. It should be pointed out, however, that these observations need to be substantiated with additional studies using other methods and, preferably, the determination of vWF levels synthesized in the tumor tissues.


Subject(s)
Colorectal Neoplasms/blood , von Willebrand Factor/metabolism , Case-Control Studies , Female , Humans , Immunoelectrophoresis , Male , Middle Aged , Prognosis
13.
J Cutan Med Surg ; 6(1): 26-8, 2002.
Article in English | MEDLINE | ID: mdl-11896421

ABSTRACT

BACKGROUND: A case of basal cell carcinoma (BCC) of the perianal region is reported. This tumor is extremely rare in this location and behaves rather innocently. OBJECTIVE: Clinical and histopathologic characteristics of perianal BCC, as well as the choices of treatment, are outlined. CONCLUSION: The tumor should be histologically distinguished from basaloid carcinoma of the anus, which is much more aggressive and metastasizes early, thus requiring a different therapy.


Subject(s)
Anus Neoplasms/pathology , Carcinoma, Basal Cell/pathology , Aged , Female , Humans
14.
Rev. bras. colo-proctol ; 1(2): 39-43, abr.-jun. 1981. tab
Article in Portuguese | LILACS | ID: lil-100271

ABSTRACT

Os autores, de acordo com os dados obtidos neste estudo, encontraram um efeito profilático da infecçäo incisional, em cirurgias prolongadas do cólon e reto, pela associaçäo da kenamicina ao preparo mecânico do cólon


Subject(s)
Adolescent , Adult , Middle Aged , Humans , Male , Female , Colon , Preoperative Care/methods , Surgical Wound Infection/prevention & control , Brazil , Kanamycin/immunology , Sulfaguanidine/immunology
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