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- W4383647308 abstract "Appendiceal tumors are rare and generally detected in appendectomy specimens with an incidence of 0.7–1.4% [1, 2]. They are difficult to diagnose without surgical interventions such as appendectomy because of its anatomical location. In addition, appendiceal neoplasms consist of heterogeneous groups, which have different histopathological subtypes according to epithelial and non-epithelial origins. Appendiceal neuroendocrine neoplasms (NENs) are non-epithelial tumors. Conversely, appendiceal mucinous neoplasms, colonic-type adenocarcinomas, goblet cell adenocarcinomas, and signet-ring cell adenocarcinomas are regarded as appendiceal tumors of epithelial origin. Although there have been no unified terminologies and classifications of these diverse histopathologic features, treatment strategies for surgical treatments of appendiceal neoplasms should be decided considering histopathological subtypes and localized or disseminated tumor status." @default.
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- W4383647308 date "2023-01-01" @default.
- W4383647308 modified "2023-09-25" @default.
- W4383647308 title "Staging and Treatment. II-3. Surgical Resection for Appendiceal Neoplasms" @default.
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- W4383647308 doi "https://doi.org/10.1007/978-981-99-0815-8_29" @default.
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