Background: An intraosseous myxoma is a rare, benign mesenchymal tumor that penetrates the bone. The occurrence of an intraosseous myxoma in the clivus is a unique presentation of the disease.
Observations: The authors discuss the case of a 15-year-old male with a new diagnosis of a primary clival intraosseous myxoma presenting with cranial nerve VI palsy. This is the third documented case of this pathology occurring in the clivus. This patient was successfully treated with endoscopic endonasal resection of the tumor.
Lessons: Primary clival intraosseous myxomas are extremely rare, but nonetheless it is important to add it to the differential diagnosis of clival masses. This mass has a high risk of recurrence, and prior literature suggests gross total resection may improve chances of progression-free survival. However, further larger studies are needed to provide guidelines regarding proper management of this pathology.
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http://dx.doi.org/10.3171/CASE22334 | DOI Listing |
Cureus
August 2024
Department of Plastic Surgery, Kobe University Graduate School of Medicine, Kobe, JPN.
Genes Chromosomes Cancer
January 2024
Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Eur Arch Paediatr Dent
August 2023
Department of Pathology, Federal University of Santa Catarina, Florianópolis, Santa Catarina, Brazil.
Purpose: This study assessed the prevalence of maxillofacial lesions in children, i.e., 0-9 years, and adolescents, i.
View Article and Find Full Text PDFJ Neurosurg Case Lessons
April 2023
2Department of Neurosurgery, Medical College of Wisconsin, Milwaukee, Wisconsin.
Background: Solitary lesions of the clivus, especially nonchordomatous ones, are exceptionally rare pathologies representing only 0.1%-0.2% of intracranial tumors that may present diagnostic and therapeutic challenges.
View Article and Find Full Text PDFAm J Surg Pathol
February 2023
Department of Pathology and Laboratory Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.
Mesenchymal tumors harboring various kinase fusions were recently recognized as emerging entities mainly in the soft tissues. We herein investigate the clinicopathologic and molecular characteristics of head and neck mesenchymal tumors harboring kinase fusions. The study cohort included 15 patients with a median age of 13 years (ranging from congenital to 63 y).
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!