ArticleCase reports in medicine2019
Ten-Year Follow-Up of Collision Tumors Composed of Craniopharyngioma and Pituitary Adenoma: A Case Report and Literature Review.
Article in Case reports in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.
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Who cites it
8 citing papers in PubMed, 1 synthesis or guideline pooled it.
- "Intrasellar tumor-to-tumor metastasis: A single center experience with a systematic review".Pituitary · 2024Pooled it
- Case Report: Sellar collision tumor consisting of pituitary adenoma and craniopharyngioma, with literature review.Frontiers in oncology · 2026Article
- Coexistence Tumor of Craniopharyngioma and Pituitary Neuroendocrine Tumor: A Case Report and Literature Review.Cureus · 2025Article
- Pituitary Adenoma Coexistent with Sellar Clear Cell Meningioma Unattached to the Dura: Case Report and Treatment Considerations.Journal of neurological surgery reports · 2024Article
- Case report: Spindle cell sarcoma and pituitary adenoma in the sella region-a rare collision tumor.Frontiers in oncology · 2024Article
- A Collision Tumor of Pit-1/SF-1-positive Double Pituitary Adenoma and a Craniopharyngioma Coexisting with Graves' Disease.NMC case report journal · 2023Article
- Papillary craniopharyngioma in a patient following resection of nonfunctioning pituitary adenoma: illustrative case.Journal of neurosurgery. Case lessons · 2021Article
- Collision Tumor in the Pituitary, Concurrent Pituitary Adenoma, and Craniopharyngioma.Case reports in otolaryngology · 2020Article
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Authors and funding
6 authors.
Funding
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Abstract
Although craniopharyngioma (CP) and pituitary adenoma (PA) are common tumors of the parasellar lesions, the coexistence of CP and PA is very rare. A 48-year-old male visited our hospital because of consciousness disturbance. The neuroimaging revealed a sellar tumor contact with a massive suprasellar cyst including calcification. Preoperative diagnosis was CP, and the patient underwent craniotomy to resolve the suprasellar mass effect. The histological examination disclosed adamantinomatous CP, and subsequently a transsphenoidal approach was chosen for the residual intrasellar tumor. Against expectations, the histological diagnosis was not CP but PA. The patient underwent gamma knife surgery for the residual tumor, and the postoperative course was good. After a 10-year follow-up, both lesions were still completely controlled. If we had suspected and diagnosed the tumor involved as not only CP but also PA at the first operation, the second operation could have been avoided because we would have chosen gamma knife surgery for the residual tumor. We should draw attention to this rare situation for differential diagnosis of parasellar tumor to avoid unnecessary surgery and to decide the best strategy for treatment. In addition, the biological behavior of collision tumors composed of CP and PA is probably the same as solitary CP or PA based on a long-term follow-up of our case.
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