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Clinicopathological Features and Management of Appendiceal Mucoceles: A Systematic Review.
Am Surg ; 84(2): 273-281, 2018 Feb 01.
Article em En | MEDLINE | ID: mdl-29580358
ABSTRACT
Appendiceal mucoceles (AMs) are rare mucin-containing neoplasms with malignant potential. Lack of evidence-based data exists defining clinicopathological features for management. MEDLINE search between 1995 and 2015 was performed using search criteria "Appendix mucocele." Systematic review of patient-, pathologic-, and treatment-related characteristics was performed and data analyzed. Among 276 cases of non-perforated AMs, 163 (59%) patients were female, with variable and nonspecific presentation. Patients were treated with appendectomy (52.1%), right hemicolectomy (17.6%), partial cecectomy (17.2%), and ileocecetomy (13.1%). Pathologic evaluation revealed the following cystadenoma/low-grade appendiceal mucinous neoplasm (54%), unspecified/benign (25%), retention cyst (14.1%), cystadenocarcinoma (4.2%), and mucosal hyperplasia (2.9%). All 11 (4.2%) patients with cystadenocarcinoma were female (P = 0.004), odds ratio for malignancy 1.07 times higher for women. Synchronous colonic malignancy was reported in three patients (27%) with cystadenocarcinoma (P = 0.007), odds ratio of 12.1. AMs have low risk for malignancy. Treatment should begin with appendectomy-only and subsequently guided by pathologic diagnosis.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Apêndice / Cistadenoma Mucinoso / Cistadenocarcinoma Mucinoso / Adenocarcinoma Mucinoso / Cistadenocarcinoma / Mucocele Tipo de estudo: Diagnostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Am Surg Ano de publicação: 2018 Tipo de documento: Article
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Apêndice / Cistadenoma Mucinoso / Cistadenocarcinoma Mucinoso / Adenocarcinoma Mucinoso / Cistadenocarcinoma / Mucocele Tipo de estudo: Diagnostic_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Am Surg Ano de publicação: 2018 Tipo de documento: Article