ArticleIndian journal of ophthalmology
Primary primitive neuroectodermal tumor of the orbit.
Article in Indian journal of ophthalmology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
5 citing papers in PubMed, 15 citations in OpenAlex.
- Primary orbital rhabdoid tumour masquerading as atypical persistent foetal vasculature.BMJ case reports · 2024Article
- Immunohistochemistry on pattern of ocular & adnexal tumours in a tertiary eye care centre of Northeast India.The Indian journal of medical research · 2018Article
- Round Cell Tumors: Classification and Immunohistochemistry.Indian journal of medical and paediatric oncology : official journal of Indian Society of Medical & Paediatric OncologyReview
- Surgical resection of orbital primitive neuroectodermal tumor without adjuvant chemotherapy.Oman journal of ophthalmologyArticle
- Peripheral primitive neuroectodermal tumor of the orbit in Graves' ophthalmopathy - A rare presentation.Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological SocietyArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Primitive neuroectodermal tumor (PNET) is a small round cell malignant tumor of neuroectodermal origin. Most of the PNETs occur in the central nervous system (CNS). PNETs recognized outside of CNS are diagnosed as peripheral PNET (pPNET). This tumor which expresses MIC-2 gene (CD99) seems to be least aggressive after complete tumor resection. We describe a rare case of PNET in a young girl.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.