Evidence map›Paper›PMID 40469374›Full record

ArticleSurgical neurology international2025

A rare case of giant infrasellar craniopharyngioma with extensive invasion of the pterygopalatine fossa: A case report and literature review.

Vittor Sérgio Santos de Quintela, Sofia Morais Silva Almeida, Arthur Campos do Nascimento, Nelson Almeida D'Ávila Melo, Arthur Maynart Pereira Oliveira

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Article in Surgical neurology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Vittor Sérgio Santos de QuintelaDepartment of Medicine, Federal University of Sergipe, Aracaju, Brazil.
Sofia Morais Silva AlmeidaDepartment of Medicine, Federal University of Sergipe, Aracaju, Brazil.
Arthur Campos do NascimentoDepartment of Medicine, Federal University of Sergipe, Aracaju, Brazil.
Nelson Almeida D'Ávila MeloDepartment of Medicine, Universidade Tiradentes, Aracaju, Brazil.
Arthur Maynart Pereira OliveiraDepartment of Neurosurgery, Hospital de Cirurgia, Aracaju, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Craniopharyngiomas are benign epithelial tumors that arise along the craniopharyngeal duct, commonly located in the sellar or suprasellar region. Infrasellar extension is a rare variant and may involve the nasopharynx, sphenoid sinus, clivus, and pterygopalatine fossa. Case Description: A 66-year-old male patient is presented to the otorhinolaryngology service due to a complaint of left ear obstruction for the past 4 months. After no response to clinical treatment, investigation with computed tomography and magnetic resonance imaging showed a heterogeneous lesion with areas of calcification and bone destruction located in the sphenoid sinus region, which projected inferiorly and laterally invading the clivus in its entirety, the petrous apex, middle fossa, pterygopalatine, and infratemporal fossae with no involvement of the sellar/suprasellar region. The patient was referred to a multidisciplinary skull base surgery group that performed an extended transpterygoid endoscopic endonasal approach with gross total resection. The anatomopathological study was consistent with adamantinomatous craniopharyngioma. Conclusion: We present a rare case of a giant infrasellar craniopharyngioma with extensive invasion of the skull base without involvement of the sella or the pituitary gland.

Indexed as

Case reportCraniopharyngiomaLiterature reviewSkull base neoplasmsSphenoid sinus

Identifiers

PMID40469374
PMCPMC12134831

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