ArticleIranian journal of pathology2018
Peripheral Primitive Neuroectodermal Tumor of the Ovary: The Report of Two Rare Cases.
Article in Iranian journal of pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed, 8 citations in OpenAlex.
- Atypical Pelvic Tumors in Children.Cancers · 2025Article
- Primary ovarian peripheral primitive neuroectodermal tumor presented with breast metastasis; Case report.Rare tumors · 2025Article
- Peripheral-type primitive neuroectodermal tumor of the ovary with EWSR1-FLI1 fusion transcript: a case report and brief review of literature.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologieReview
- Primitive neuroectodermal tumors of the ovary: a multidecade review of the scientific literature.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologieArticle
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Authors and funding
5 authors at 1 institution in 1 country.
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Abstract
Peripheral primitive neuroectodermal tumor (pPNET) is a highly aggressive small round cell tumor belonging to PNET/Ewing sarcoma family. Ovarian tumors composed of primitive neuroectodermal elements are extremely rare. Herein we reported two cases of peripheral primitive neuroectodermal tumors of ovary in two patients with different clinical presentations. Definite diagnoses were made based on the histomorphology and immunohistochemistry results. With respect to different clinical behaviors, treatment modalities and prognosis of peripheral primitive neuroectodermal tumors compared to other known ovarian neoplasms, it is essential to consider this entity as a differential diagnosis in ovarian tumors especially in young patients.
Indexed as
Identifiers
30774687PMC6358556W2897116424What OpenQuestion holds
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