Tumor neuroectodérmico primitivo

Authors

  • Mónica Gabriela Larcos Andrade

DOI:

https://doi.org/10.29166/rfcmq.v43i2.2835

Keywords:

Neuroepithelioma, Ewing’s sarcoma

Abstract

A primitive neuroectodermal tumor (PPNET) or peripheral neuroepithelioma is a malignant neoplasm of small round blue cells derived from the neural crest. It is one of the most undifferentiated histological types among malignant tumors, because it is indistinguishable from Ewing’s sarcoma from the imaging and histology perspective. It considers a single pathology for this paper. It can appear in childhood or more frequently in adolescence; treatment includes chemotherapy, surgery, and radiation therapy. We present the clinical case of a 77-year-old patient who consulted for palpebral ptosis, and it classifies as Horner’s Syndrome. The final diagnosis was a peripheral neuroectodermal tumorconfirmed with histopathology and immunohistochemistry.

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Author Biography

Mónica Gabriela Larcos Andrade

Servicio de Oftalmología, Hospital Carlos Andrade Marín, Quito-Ecuador

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Published

2018-12-01

How to Cite

1.
Larcos Andrade MG. Tumor neuroectodérmico primitivo . Rev Fac Cien Med (Quito) [Internet]. 2018 Dec. 1 [cited 2024 Jun. 30];43(2):167-70. Available from: https://revistadigital.uce.edu.ec/index.php/CIENCIAS_MEDICAS/article/view/2835