Pituicytoma: Report of three cases and a systematic literature review
Pituicytoma is a rare subtype of WHO grade I glioma that originates in the neurohypophysis or infundibulum. Here we presented 3 cases of histopathologically diagnosed pituicytoma and subsequently performed a corresponding systematic literature review. A comprehensive literature search of the PubMed...
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Veröffentlicht in: | Clinical neurology and neurosurgery 2021-06, Vol.205, p.106650-106650, Article 106650 |
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Sprache: | eng |
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Zusammenfassung: | Pituicytoma is a rare subtype of WHO grade I glioma that originates in the neurohypophysis or infundibulum. Here we presented 3 cases of histopathologically diagnosed pituicytoma and subsequently performed a corresponding systematic literature review. A comprehensive literature search of the PubMed database was conducted. A total of 77 studies were eventually reviewed and 168 pituicytoma cases were identified. The epidemiology, clinical manifestations, radiological features, treatment, and pathological findings of all previous pituicytoma cases were summarized, and a “portrait” of this rare tumor was shown. It is hoped that the current study will afford a broader and more adequate understanding upon this rare disease.
•This is the most comprehensive literature review for pituicytoma so far.•The characteristics of 168 pituicytoma patients are summarized and discussed.•The current study can further our understanding upon this rare disease. |
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ISSN: | 0303-8467 1872-6968 |
DOI: | 10.1016/j.clineuro.2021.106650 |