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ReviewChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2025

Brown tumor in the pterygopalatine fossa with maxillary and sphenoidal involvement: a rare case report and literature review.

Ali Naeim, Amirhossein Larijani, Arvin Naeimi, Jahangir Ghorbani, Alireza Sadeghipour, Mohammad Shirani

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Review in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 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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6 authors.

Ali NaeimDepartment of Neurosurgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Amirhossein LarijaniDepartment of Neurosurgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-2282-2924
Arvin NaeimiStudent Research Committee, School of Medicine, Guilan University of Medical Sciences, Rasht, Gilan, Iran.ORCID 0000-0002-8659-9549
Jahangir GhorbaniDepartment of Otorhinolaryngology, Masih Daneshvari Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Alireza SadeghipourDepartment of Pathology, Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Mohammad ShiraniDepartment of Neurosurgery, Sina Hospital, Tehran University of Medical Sciences, Tehran, Iran. shiranibmohamad@gmail.com.

Funding

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6 · The paper itself

Abstract

Brown tumors are rare focal giant-cell lesions resulting from the direct effects of parathyroid hormone (PTH) on bone tissue in hyperparathyroidism. Brown tumors most commonly affect long bones, pelvis, and ribs, whereas craniofacial involvement is uncommon, with pterygopalatine fossa involvement being exceedingly rare. This report presents a case of a 13-year-old girl with a rapidly progressing lesion in the pterygopalatine fossa, with involvement of the sphenoid and maxilla. The patient exhibited significant facial pain and V2 paresthesia, with imaging studies suggesting differential diagnoses such as craniopharyngioma and glioma. Pre-operative digital subtraction angiography ruled out highly vascular lesions, and the patient underwent complete tumor resection via an expanded endoscopic transnasal approach. Histopathological evaluation initially revealed a solid-variant aneurysmal bone cyst (ABC). Nevertheless, routine postoperative laboratory evaluation incidentally detected a significant increase in PTH and hypercalcemia, prompting further pathological reassessment and confirming the diagnosis of a brown tumor. Finally, the patient underwent a parathyroidectomy, followed by further management and regular follow-ups. This case highlights the diagnostic challenges posed by the histopathological overlap between brown tumors and other giant-cell lesions, such as ABCs and giant-cell tumors, particularly in their rare presentation in the pterygopalatine fossa. The choice of surgical approach was guided by the lesion's location, symptom severity, and rapid progression, demonstrating the utility of ipsilateral transmaxillary endoscopic techniques in accessing complex anatomical regions. Furthermore, this case underscores the importance of routine calcium and PTH testing in preoperative evaluations of cranial bone lesions to prevent potential misdiagnosis and ensure accurate, effective, and timely management.

Indexed as

MaxillaOsteitis Fibrosa CysticaPterygopalatine FossaSphenoid BoneAdolescentFemaleHumansBrown tumorOsteitis fibrosa cysticaOsteoclastomasSolid-variant aneurysmal bone cyst

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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.