ABSTRACT
BACKGROUND: Non-operative management has been suggested as a therapy for uncomplicated appendicitis. Notwithstanding, the risk of missing an appendiceal tumor must be considered, being the surgical piece crucial to rule out neoplasms. Therefore, we aim to determine the incidence of appendiceal neoplasms in patients with acute appendicitis, tumor types and the importance of the anatomopathological study of the surgical piece. STUDY DESIGN: Retrospective study in which we described patients who underwent emergent appendectomy with histopathological findings of appendiceal neoplasms from January 2012 to September 2018. Descriptive analysis included demographic variables, diagnostic methods, and surgical techniques. RESULTS: 2993 patients diagnosed with acute appendicitis who underwent an emergency appendectomy. 64 neoplasms of the appendix were found with an incidence of 2,14%. 67.2% were women, the mean age was 46,4 years (± 19.5). The most frequent appendiceal neoplasms were neuroendocrine tumors (42,2%), followed by appendiceal mucinous neoplasms (35,9%), sessile serrated adenomas (18,8%), and adenocarcinomas (3,1%). In 89,1% of the cases, acute appendicitis was determined by imaging, and 14% of cases were suspected intraoperatively. Appendectomy was performed in 78,1% without additional procedures. CONCLUSIONS: Appendiceal tumors are rare and must be ruled out in patients with suspected acute appendicitis. The incidence of incidental neoplasms is higher in this study than in the previously reported series. This information must be included in decision-making when considering treatment options for acute appendicitis.
Subject(s)
Adenocarcinoma , Appendiceal Neoplasms , Appendicitis , Humans , Female , Male , Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/surgery , Appendectomy , Incidence , Appendicitis/epidemiology , Appendicitis/surgery , Retrospective Studies , Adenocarcinoma/epidemiology , Adenocarcinoma/surgeryABSTRACT
BACKGROUND: Adenocarcinomas of the appendix are rare cancers for which no National Comprehensive Cancer Network guidelines exist, and for patients who undergo resection with curative intent, there is a paucity of data on prognostic factors affecting long-term cancer-specific survival. We aimed to compare the cancer-specific survival outcomes in adult patients with appendiceal non-mucinous adenocarcinoma undergoing either local resection versus right hemicolectomy. METHODS: This was a retrospective study from the National Cancer Institute Surveillance, Epidemiology, and End Results of patients who underwent curative resection over a 15-year period (2004-2019) for primary appendiceal adenocarcinoma. Out of 16,699 patients, 14,945 were excluded (exclusion criteria were non-adenocarcinoma histological types and patients with regional or distant metastasis as per National Cancer Institute Surveillance, Epidemiology, and End Results stage). Effects of factors (age, race, tumor biology [mucinous versus non-mucinous tumors], the extent of resection of the primary lesion, and lymph nodes) on cancer-specific long-term survival were studied. Survival analysis was performed using the Kaplan-Meier method. Survival outcomes were reported as mean survival (months). RESULTS: Of 1,754 patients, 827 (47.1%) were women, and 927 (52.1%) were men. The mean age in years (± standard deviation) was 62.43 ± 14.3. The racial distribution was as follows: Black 237 (13.5%), White 1,398 (79.7%), and Other 119 (6.8%). A total of 771 (44.6%) underwent local resection (appendectomy or segmental resection of colon without lymph node resection), and 983 (55.4%) underwent hemicolectomy with lymph node resection. Favorable survival prognosticators were age <50 years, White race, and well-differentiated histology. Patients with mucinous tumors experienced better survival. Patients who underwent right hemicolectomy with lymph node resection experienced better survival compared with those who had an appendectomy or segmental colonic resection for non-mucinous tumors rather than mucinous tumors. CONCLUSION: We report novel demographic, tumor-related, and operative prognostic factors impacting long-term cancer-specific survival in patients who undergo resection for appendiceal adenocarcinoma. The extent of resection of the primary lesion with draining lymph nodes determines long-term cancer-specific survival in non-mucinous appendiceal adenocarcinomas.
Subject(s)
Adenocarcinoma, Mucinous , Adenocarcinoma , Appendiceal Neoplasms , Male , Adult , Humans , Female , Middle Aged , Retrospective Studies , Adenocarcinoma, Mucinous/pathology , Survival Analysis , Colectomy/methods , Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/surgeryABSTRACT
INTRODUCTION: The prevalence of appendiceal endometriosis ranges from 0.4% to 22%. The carcinoid tumor is the most common neoplasm of the appendix, with incidence ranging from 0.3% to 0.9%. Appendix lesions develop in up to 22% of women with deep infiltrative endometriosis. Even though these are most likely endometriosis, carcinoid tumors should always be considered. The aim of this review was to assess the prevalence of appendiceal carcinoid tumors and appendiceal endometriosis in patients undergoing gynecologic surgery, its association with endometriosis, and related symptoms. EVIDENCE ACQUISITION: We included retrospective and prospective studies that assessed women who underwent appendicectomy in the past 20 years for appendiceal endometriosis and/or appendix carcinoid tumor confirmed by histological analysis. Results were reported as relative and absolute frequencies. Due to the heterogeneity of included studies, a statistical analysis (meta-analysis) was not performed. EVIDENCE SYNTHESIS: The prevalence of appendiceal endometriosis was 15.2% in patients who underwent surgery for pelvic endometriosis and 11.4% in those who underwent benign gynecological surgery. Conversely, carcinoid tumors of the appendix were present in 2.4% of endometriosis patients and 1.3% of other benign gynecological surgeries. CONCLUSIONS: The rates of carcinoid tumors in patients with endometriosis are the same as in the general population. Given the risk of a malignant appendiceal tumor, in all gynecological surgeries, especially those for endometriosis, the appendix should be inspected and removed if it has an abnormal appearance.
Subject(s)
Appendiceal Neoplasms , Appendix , Carcinoid Tumor , Endometriosis , Appendiceal Neoplasms/epidemiology , Appendix/surgery , Carcinoid Tumor/epidemiology , Endometriosis/epidemiology , Female , Humans , Prospective Studies , Retrospective StudiesABSTRACT
Appendiceal neoplasms include a heterogeneous group of epithelial and nonepithelial tumors that exhibit varying malignant potential. This review article summarizes current diagnostic criteria, classification systems, and optimal therapeutic strategies for the five main histopathologic subtypes of appendiceal neoplasms. In particular, the management of epithelial appendiceal neoplasms has evolved. Although their treatment has historically been extrapolated from colon cancer, improved understanding of their unique histopathologic and molecular characteristics and a growing body of published clinical data support a more nuanced approach to their management.
Subject(s)
Appendiceal Neoplasms , Appendiceal Neoplasms/diagnosis , Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/therapy , Humans , Neoplasms, Glandular and EpithelialABSTRACT
Introduction: Carcinoid tumors are neuroendocrine malignancies that originate in the neuroectodermal cells of the Amine, Peptide Uptake and Decarboxylation system dispersed in the gastrointestinal mucosa and representing about 80-88% of tumors of cecal appendix. These are tumors usually diagnosed at appendectomies, and it is estimated that from each 100 appendectomies yearly performed, at least one case is a neuroendocrine tumor. Objectives: To report the experience of an University Teaching Hospital in health and reference at the east side of São Paulo and great São Paulo in cases of these rare appendicular tumors, with emphasis on the importance of these descriptions, as probably are rare those surgeons in particular who will acquire extensive wisdom in these cases. Method: Retrospective analysis of 237 patients who underwent appendectomy from September 2010 to September 2012 in the Hospital Santa Marcelina-SP. We evaluated data on age, gender, initial clinical presentation and surgical findings of patients undergoing appendectomy with subsequent anatomic and immunopathological diagnosis of carcinoid tumor of cecal appendix. Results: The presence of a carcinoid tumor of the appendix was observed in 5 patients, which corresponds to 2.1% of all appendectomies performed. Regarding gender, 4 patients (80%) were female and the average age was 34.2 years, with a range from 17 to 68 years. In all patients the initial hypothesis for surgery indication was acute appendicitis, with an intraoperative finding of necroperforated phase acute appendicitis in 3 patients (60%). Conclusion: The therapeutical conduct after the diagnosis of carcinoid tumors of the appendix must be based on the data provided by pathological and immunohistochemical studies, besides the judicious judgment of the attending physician. (AU)
Introdução: Os tumores carcinoides são neoplasias malignas neuroendócrinas que se originam em células neuroectodérmicas do sistema APUD (Amine, Peptide Uptake and Decarboxylation), dispersas na mucosa gastrointestinal e que representam cerca de 80-88% das neoplasias do apêndice cecal. São tumores diagnosticados geralmente durante apendicectomias e estima-se que de cada 100 apendicectomias realizadas por ano, ao menos um caso será TNE. Objetivos: Objetiva-se nesse artigo relatar experiência de Hospital Universitário e de Ensino (HUE) em saúde e referência na zona leste de São Paulo e grande São Paulo em casos desses raros tumores apendiculares, com ênfase na importância dessas descrições, já que provavelmente raros cirurgiões em particular irão adquirir uma extensa sapiência nesses casos. Método: Análise retrospectiva de 237 pacientes submetidos à apendicectomia no período de setembro de 2010 a setembro de 2012 no Hospital Santa Marcelina-SP. Foram avaliados os dados referentes a idade, sexo, quadro clínico inicial, achados operatórios dos pacientes submetidos à apendicectomia com posterior diagnóstico anatomopatológico e imunopatológico de tumor carcinoide de apêndice. Resultados: Verificou-se a presença de tumor carcinoide de apêndice em 5 pacientes, o que corresponde a 2,1% das apendicectomias realizadas. Com relação ao gênero, 4 pacientes (80%) eram mulheres e a média de idade foi de 34,2 anos, com variação de 17 a 68 anos. Em todos os pacientes a hipótese inicial para indicação de cirurgia fora de apendicite aguda, com achado intra-operatório de apendicite aguda em fase necroperfurada em 3 pacientes (60%). Conclusão: A conduta após o diagnóstico de tumores carcinoides de apêndice cecal deve ser alicerçada nos dados fornecidos por exames anatomopatológicos e imunoistoquímicos, além do julgamento criterioso do médico assistente. (AU)
Subject(s)
Humans , Male , Female , Appendiceal Neoplasms/epidemiology , Carcinoid Tumor/epidemiology , Appendectomy , Appendiceal Neoplasms/pathology , Neoplasm StagingABSTRACT
Background: The most common malignant appendicular neoplasm is the neuroendocrine well-differentiated tumor (NET). Other malignant tumors are uncommon, reported with a frequency of 0.2 percent of all appendectomies. Aim: To describe the characteristics of appendiceal malignant tumors found in regional hospitals of Northern Chile. Material and Methods: All patients operated for acute appendicitis between 2005 and 2011, in which a malignant appendiceal tumor was found in the pathological study, were analyzed. Clinical and survival information was obtained from medical records and national death registries. Results: We analyzed 8.972 appendectomy records. Appendicular tumors were found in 40 patients (0.4 percent). Thirty patients (0.3 percent) had malignant tumors. NET was the most common tumor found in 19 patients (63 percent). The tumor was smaller than 1 cm in 16 cases (53 percent). In 5 patients (17 percent), the tumor was larger than 2 cm with the appendicular base infiltrated by malignant cells. Most patients (83 percent) presented with stage I tumors. In 23 patients (77 percent, the appendectomy was considered sufficient and definitive treatment. Conclusions: In this series of patients, appendicular tumors had similar characteristics to those reported abroad. All patients had a favorable evolution without associated mortality or tumor relapse...
Introducción: El tumor apendicular maligno encontrado con mayor frecuencia es el tumor neuroendocrino bien diferenciado (NET). Otros tumores malignos se reportan con una frecuencia menor a 0,2 por ciento de todas las apendicectomías. El objetivo del presente estudio es describir las características de los tumores malignos del apéndice en la IV Región de Chile. Material y Método: Se estudió una cohorte histórica constituida por pacientes operados en los hospitales de La Serena, Coquimbo y Ovalle entre enero de 2005 y diciembre de 2011. Los resultados se reportan mediante estadística descriptiva. Resultados: Se estudiaron 8.972 apendicectomías. En 40 pacientes (0,4 por ciento) se diagnosticaron tumores apendiculares de los cuales 30 (0,3 por ciento) fueron malignos y fueron incluidos en este análisis. El tipo histológico maligno más frecuente fue el NET en 19 casos (63 por ciento). En 16 casos (53 por ciento) el tumor fue menor a 1 cm. En 5 casos (17 por ciento) el tumor fue mayor a 2 cm con compromiso de la base. La mayoría de los pacientes (83 por ciento) se presentaron con tumores en estadio I y los demás con tumores en estadio II. En 23 pacientes (77 por ciento) la apendicectomía fue considerada como el tratamiento definitivo. Conclusiones: Las características generales de los tumores malignos del apéndice en los pacientes operados por apendicitis en la IV Región de Chile son similares a las características reportadas en series nacionales e internacionales. En la presente cohorte, los pacientes tuvieron una evolución favorable sin mortalidad asociada al tumor y sin recurrencias conocidas hasta la fecha actual...
Subject(s)
Humans , Male , Female , Appendectomy/statistics & numerical data , Appendiceal Neoplasms/surgery , Appendiceal Neoplasms/epidemiology , Chile , Follow-Up Studies , Appendiceal Neoplasms/pathology , Retrospective Studies , Survival RateABSTRACT
CONTEXT: The development of neoplasia is an important concern associated with inflammatory bowel disease (IBD), especially colorectal cancer (CRC). OBJECTIVES: Our aim was to determine the incidence of intestinal and extraintestinal neoplasias among patients with inflammatory bowel disease. METHODS: There were retrieved information from 1607 patients regarding demographics, disease duration and extent, temporal relationship between IBD diagnosis and neoplasia, clinical outcomes and risk factors for neoplasia. RESULTS: Crohn's disease (CD) was more frequent among women (P=0.0018). The incidence of neoplasia was higher in ulcerative colitis (UC) when compared to CD (P=0.0003). Eight (0.99%) patients developed neoplasia among 804 with CD: 4 colorectal cancer, 2 lymphomas, 1 appendix carcinoid and 1 breast cancer. Thirty (3.7%) patients developed neoplasia among the 803 UC: 13 CRC, 2 lymphomas and 15 extraintestinal tumors. While CRC incidence was not different among UC and CD (1.7% vs 0.5%; P=0.2953), the incidence of extraintestinal neoplasias was higher among UC (2.1% vs 0.5%, P=0.0009). Ten (26.3%) patients out of 38 with neoplasia died. CONCLUSIONS: CRC incidence was low and similar in both diseases. There was a higher incidence of extraintestinal neoplasia in UC when compared to CD. Neoplasias in IBD developed at a younger age than expected for the general population. Mortality associated with malignancy is significant, affecting 1/4 of the patients with neoplasia.
Subject(s)
Appendiceal Neoplasms/etiology , Breast Neoplasms/etiology , Colitis, Ulcerative/complications , Colorectal Neoplasms/etiology , Crohn Disease/complications , Lymphoma/etiology , Adolescent , Adult , Aged , Appendiceal Neoplasms/epidemiology , Breast Neoplasms/epidemiology , Child , Colitis, Ulcerative/epidemiology , Colorectal Neoplasms/epidemiology , Crohn Disease/epidemiology , Female , Humans , Incidence , Lymphoma/epidemiology , Male , Middle Aged , Risk Factors , Tertiary Healthcare , Young AdultABSTRACT
Context The development of neoplasia is an important concern associated with inflammatory bowel disease (IBD), especially colorectal cancer (CRC). Objectives Our aim was to determine the incidence of intestinal and extraintestinal neoplasias among patients with inflammatory bowel disease. Methods There were retrieved information from 1607 patients regarding demographics, disease duration and extent, temporal relationship between IBD diagnosis and neoplasia, clinical outcomes and risk factors for neoplasia. Results Crohn's disease (CD) was more frequent among women (P = 0.0018). The incidence of neoplasia was higher in ulcerative colitis (UC) when compared to CD (P = 0.0003). Eight (0.99%) patients developed neoplasia among 804 with CD: 4 colorectal cancer, 2 lymphomas, 1 appendix carcinoid and 1 breast cancer. Thirty (3.7%) patients developed neoplasia among the 803 UC: 13 CRC, 2 lymphomas and 15 extraintestinal tumors. While CRC incidence was not different among UC and CD (1.7% vs 0.5%; P = 0.2953), the incidence of extraintestinal neoplasias was higher among UC (2.1% vs 0.5%, P = 0.0009). Ten (26.3%) patients out of 38 with neoplasia died. Conclusions CRC incidence was low and similar in both diseases. There was a higher incidence of extraintestinal neoplasia in UC when compared to CD. Neoplasias in IBD developed at a younger age than expected for the general population. Mortality associated with malignancy is significant, affecting 1/4 of the patients with neoplasia. .
Contexto O desenvolvimento de neoplasias se constitui em preocupação constante em pacientes com doenças inflamatórias intestinais (DII), especialmente o câncer colorretal (CCR). Objetivos Determinar a incidência de neoplasias intestinais e extra-intestinais entre pacientes com DII. Métodos Foram obtidas informações de 1607 pacientes, quanto a dados demográficos, duração e extensão da doença, relação temporal entre diagnóstico das DII e neoplasia, evolução clínica e fatores de risco para neoplasia. Resultados Doença de Crohn (DC) foi mais frequente entre as mulheres (P = 0.0018). A incidência de neoplasia foi maior nos doentes com retocolite ulcerativa (RCU) em relação aos com DC (P = 0.0003). Oito (0.99%) pacientes desenvolveram neoplasia entre 804 com DC: quatro tumores colorretais, dois linfomas, um carcinóide de apêndice e um câncer de mama. Trinta (3.7%) pacientes desenvolveram neoplasia entre os 803 RCU: 13 CCR, 2 linfomas e 15 tumores extra-intestinais. Enquanto a incidência de CCR não diferiu entre RCU e DC (1.7% vs 0.5%; P = 0.2953), a incidência de neoplasias extraintestinais foi maior na RCU (2.1% vs 0.5%, P = 0.0009). Dez (26.3%) pacientes de um total de 38 com neoplasia, evoluíram a óbito durante o seguimento. Conclusões A incidência de CCR foi baixa e similar em ambas as doenças inflamatórias. Observou-se incidência maior de neoplasia extra-intestinal na RCU quando comparada à DC. Neoplasias em doenças inflamatórias se desenvolveram em idade mais precoce do que a esperada para a população geral. A mortalidade associada a neoplasias é significativa, afetando 1/4 dos pacientes. .
Subject(s)
Adolescent , Adult , Aged , Child , Female , Humans , Male , Middle Aged , Young Adult , Appendiceal Neoplasms/etiology , Breast Neoplasms/etiology , Colitis, Ulcerative/complications , Colorectal Neoplasms/etiology , Crohn Disease/complications , Lymphoma/etiology , Appendiceal Neoplasms/epidemiology , Breast Neoplasms/epidemiology , Colitis, Ulcerative/epidemiology , Colorectal Neoplasms/epidemiology , Crohn Disease/epidemiology , Incidence , Lymphoma/epidemiology , Risk Factors , Tertiary HealthcareABSTRACT
Background: The incidence of carcinoid tumors (CT) has increased in the last five decades. These supposedly benign tumors may not always behave as such. The largest series of CT show that the most common primary tumor site (appendiceal) changed over the years. Aim: To evaluate the management of gastrointestinal CT at the National Cancer Institute from 2000 to 2006, describe their anatomic location and estimate disease specific survival. Material and Methods: Review of the database of the Cancer Committee, during a period of 7 years, looking for patients with a pathological diagnosis of CT, whose clinical records were analyzed. Results: The records of 25 patients with gastrointestinal CT, aged 18 to 79 years (19 females) were analyzed. Five years disease specific survival was 91.1 percent. The most common location was appendiceal in 56 percent of cases, with a 5 years disease specific survival of 100 percent. Right hemicolectomy was performed in seven patients with appendiceal carcinoid. Other seven patients only underwent appendectomy. Five years disease specific survival was 100 percent in both groups. Conclusions: The appendix is still the most common location of CT in this series and long term survival is acceptable.
Los tumores carcinoides (TC) gastrointestinales han aumentando su incidencia en las últimas 5 décadas. Inicialmente estos tumores eran considerados de comportamiento benigno, sin embargo, con el tiempo han mostrado ser capaces de diseminarse y tener una evolución más agresiva. En general se considera al apéndice cecal como la ubicación más frecuente de TC pero esto ha cambiado en el último tiempo según publicaciones internacionales. El objetivo de este trabajo es presentar nuestra experiencia en el manejo de los TC gastrointestinales en el período 2000-2006 en el Instituto Nacional del Cáncer (INC) reportando una serie de casos, describir su ubicación anatómica y estimar la sobrevida específica de enfermedad. Método: Estudio descriptivo. Se revisó la base de datos del Comité Oncológico del INC, durante un período de 7 años, incluyendo pacientes con diagnóstico anatomopatológico de TC. Se revisaron las fichas clínicas y se recolectaron registros de defunción. Resultados: 25 pacientes con diagnóstico de TC confirmado por patología, presentando una sobrevida específica de enfermedad a 5 años de 91,1 por ciento. La ubicación más frecuente de TC fue apéndice cecal (56 por ciento) y este grupo de pacientes presenta sobrevida específica de enfermedad de 100 por ciento a 5 años. De los TC apendiculares, en 7 pacientes se realizó una hemicolectomía derecha en un segundo tiempo, y en 7 pacientes sólo se realizó apendicectomía, con sobrevida específica de enfermedad de 100 por ciento en ambos grupos a 5 años (p = 0,475). Conclusiones: El apéndice cecal continúa siendo el lugar más frecuente de presentación del TC y la sobrevida alejada es adecuada en esta serie de pacientes.
Subject(s)
Humans , Male , Female , Adolescent , Adult , Middle Aged , Gastrointestinal Neoplasms/surgery , Gastrointestinal Neoplasms/mortality , Carcinoid Tumor/surgery , Carcinoid Tumor/mortality , Chile , Cancer Care Facilities/statistics & numerical data , Neoplasm Invasiveness , Neoplasm Metastasis , Neoplasm Recurrence, Local , Gastrointestinal Neoplasms/pathology , Appendiceal Neoplasms/epidemiology , Retrospective Studies , Survival Analysis , Malignant Carcinoid Syndrome/epidemiology , Carcinoid Tumor/pathologyABSTRACT
Introdução: Este artigo descreve os resultados de uma coorte retrospectiva dos pacientes da ISCMPA, discutindo as características do tumor carcinoide quando localizado no apêndice. Métodos: Foram revisados os registros do banco de dados do Serviço de Patologia da ISCMPA de todas as apendicectomias realizadas entre 2000 e 2007 com posterior revisão manual dos registros de cada paciente. Resultados: Foram identificadas 3.730 apendicetomias. A prevalência de tumores carcinoides foi 0,4%. A idade mediana do paciente ao diagnóstico de tumor carcinoide foi de 26 anos, com uma distância interquartil de 20 anos. O sexo mais acometido foi o masculino. Em 46,67% dos casos, a extremidade distal foi o local do tumor e em 40% dos casos o tumor ultrapassou a camada serosa. Conclusões: Houve dificuldades em se definir claramente se as alterações no apêndice identificadas no transoperatório correspondiam a tumor carcinoide. A congelação no transoperatório ajudou a definir o tipo de tratamento cirúrgico mais adequado e a identificar metástases de outras patologias sistêmicas
Introduction: This paper describes the results of a retrospective cohort of patients of the ISCMPA, discussing the features of carcinoid tumors occurring in the appendix. Methods: We searched the database of the ISCMPA Department of Pathology for all the records of appendectomies performed between 2000 and 2007, with subsequent manual review of individual patient records. Results: 3,730 appendectomies were identified. The prevalence of carcinoid tumors was 0.4%. The median age at diagnosis of carcinoid tumor was 26 years with an interquartile range of 20 years. Males were more affected than females. In 46.67% of the cases the distal end was the site of the tumor and in 40% the tumor exceeded the serosa layer. Conclusions: There were difficulties in clearly defining if the changes in the appendix identified during surgery corresponded to a carcinoid tumor. Transoperative freezing helped determine the most appropriate type of surgical approach and identify metastases of other systemic diseases
Subject(s)
Humans , Male , Female , Appendectomy/statistics & numerical data , Appendiceal Neoplasms/epidemiology , Carcinoid Tumor/epidemiology , Appendiceal Neoplasms/pathology , Appendix/anatomy & histology , Appendix/pathology , Brazil/epidemiology , Carcinoid Tumor/pathology , Retrospective StudiesABSTRACT
AIM: To determine the prevalence, histologic types and clinical features of primary epithelial tumours of the vermiform appendix in a predominantly black population. METHODS: All cases of primary tumours of the appendix identified by review of the histopathology records at the University of the West Indies between January 1987 and June 2007 were selected. Relevant pathologic and clinical data were extracted with supplementation from patient charts where available. Non-epithelial tumours were excluded. The total number of appendectomy specimens over the period was also ascertained. RESULTS: Forty-two primary epithelial tumours were identified out of 6,824 appendectomies yielding a prevalence rate of approximately 0.62%. Well-differentiated neuroendocrine cell tumours (carcinoids, 47.6%) and benign non-endocrine cell tumours (adenomas, 45.2%) were most common with nearly equal frequency. The median age was 43 years, with no sex predilection. Carcinoid tumours occurred in younger patients (mean age 32 years), with a male-to-female ratio of 1.2:1. A clinical diagnosis of acute appendicitis was the most common reason for appendectomy (57.1%) and was histologically confirmed in 75% (18 of 24) of cases. In total, 16.7% of cases were diagnosed after incidental appendectomy. CONCLUSION: Appendiceal epithelial tumours are rare in our experience, and are represented principally by carcinoid tumours and adenomas. Carcinoid tumours occurred in younger patients but were slightly more common in men than women. Tumours were not suspected clinically and were diagnosed incidentally in specimens submitted for acute appendicitis supporting the need for histological evaluation in all resection specimens.
Subject(s)
Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/pathology , Black People/statistics & numerical data , Adenocarcinoma/epidemiology , Adenocarcinoma/pathology , Adenoma/epidemiology , Adenoma/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Appendiceal Neoplasms/surgery , Carcinoid Tumor/epidemiology , Carcinoid Tumor/pathology , Female , Humans , Male , Middle Aged , Prevalence , Retrospective Studies , West Indies/epidemiology , Young AdultSubject(s)
Humans , Male , Adult , Adenocarcinoma/pathology , Appendiceal Neoplasms/pathology , Carcinoid Tumor/pathology , Adenocarcinoma/epidemiology , Adenocarcinoma/surgery , Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/surgery , Carcinoid Tumor/epidemiology , Carcinoid Tumor/surgery , PrognosisSubject(s)
Humans , Male , Adult , Appendiceal Neoplasms/pathology , Adenocarcinoma/pathology , Carcinoid Tumor/pathology , Appendiceal Neoplasms/epidemiology , Appendiceal Neoplasms/surgery , Carcinoid Tumor/surgery , Carcinoid Tumor/epidemiology , Adenocarcinoma/surgery , Adenocarcinoma/epidemiology , PrognosisABSTRACT
Se realizó un estudio descriptivo-retrospectivo de 8 pacientes con tumores de apéndice cecal, en el período comprendido entre el 1 de enero de 1990 y el 1 de enero de 1997, los cuales fueron intervenidos quirúrgicamente en el Hospital Provincial Clinicoquirúrgico Docente "Dr. Gustavo Aldereguía". Se revisaron todos los libros de biopsias del Departamento de Anatomía Patológica correspondientes al período analizado, para obtener aquellos casos con diagnóstico de afección tumoral de apéndice. Se estudiaron las historias clínicas y se recogieron datos de interés como sexo, manifestaciones clínicas, diagnóstico presuntivo, diagnóstico anatomopatológico y tipo de intervención. La afección tumoral de apéndice cecal es frecuente y constituyó el 0.38 por ciento del total de 20057 apéndices examinadas. No se hallaron diferencias respecto al sexo. Hubo un ligero predominio en pacientes con edades de más de 60 años. Los hallazgos clínicos más frecuentes fueron dolor agudo en fosa inguinal derecha y fiebre, con predominio del adenocarcinoma. Los principales resultados se exponen en tablas(AU)