Well-Differentiated Neuroendocrine Tumor of the Appendix

Autores/as

  • Meilany Feronika Durry Department of Anatomical Pathology, Faculty of Medicine, Sam Ratulangi University, Indonesia http://orcid.org/0000-0003-3672-9162
  • Poppy Magdalena Lintong Department of Anatomical Pathology, Faculty of Medicine, Sam Ratulangi University, Indonesia

Palabras clave:

Appendix, human and health, neuroendocrine tumor

Resumen

Appendiceal Neuroendocrine Tumors (NET) comprise rare tumors of the appendix, mainly affecting young populations and characterized by a rather favorable prognosis. Appendiceal NET is either asymptomatic or present as acute appendicitis, which is then diagnosed incidentally during surgery. We reported the case of a 9-year-old girl presenting with the common appendicitis symptoms of fever and abdominal pain.


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Publicado

2022-06-02

Cómo citar

Durry, M. F., & Lintong, P. M. (2022). Well-Differentiated Neuroendocrine Tumor of the Appendix. Gaceta Médica De Caracas, 130(1 S), S64-S67. Recuperado a partir de https://saber.ucv.ve/ojs/index.php/rev_gmc/article/view/23885

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ARTÍCULOS ORIGINALES

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