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Background: Capillary hemangiomata are benign vascular tumors that typically occur in children. They rarely occur in the central nervous system. Intracranial capillary hemangiomata in adults are very rare entities with only 18 cases reported in the literature. We report a case of parasellar capillary hemangiomata that extended into the sella in a 64-year-old woman as well as a review of the literature in adults.
Case Description: We report a 64-year-old patient who presented with a headache, left-sided paresthesia, and weakness. Initial computed tomography of her brain showed a left-sided 3 cm × 2.5 cm parasellar lesion with intrasellar extension and no mass effect. Subsequent magnetic resonance imaging (MRI) showed a lesion that was homogenously hyperintense on T2-weighted MRI and fluid-attenuated inversion recovery, isointense with adjacent brain parenchyma on T1-weighted MRI, and which demonstrated enhancement after contrast administration. The patient initially underwent an endoscopic transsphenoidal biopsy, which was inconclusive, followed by a craniotomy, biopsy, and debulking. Histologic examination showed fibrous tissue containing numerous thin-walled and irregular vascular channels of varying sizes. There was a very mild associated inflammatory infiltrate, mainly formed of small mononuclear chronic inflammatory cells and occasional histiocytes. The histologic appearances were in keeping with capillary hemangiomata.
Conclusions: Capillary hemangiomata related to the sella are very rare and can easily be misdiagnosed on imaging alone. The present case highlights capillary hemangiomata as an important, albeit rare, differential when considering a sellar or parasellar mass.
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http://dx.doi.org/10.1016/j.wneu.2018.12.185 | DOI Listing |
Radiol Case Rep
November 2025
Department of Radiology, Tokushima University Hospital, 3-18-15, Kuramoto-cho, Tokushima City, Tokushima, 770-8503, Japan.
Adrenal capillary hemangiomas are an extremely rare tumor type, and no previous studies have described their features using dynamic contrast-enhanced computed tomography. We report the case of a 65-year-old male patient with a history of right partial nephrectomy for renal clear cell carcinoma. During follow-up, computed tomography scans revealed growth of a right adrenal nodule.
View Article and Find Full Text PDFS D Med
June 2025
Department of Neurology, University of South Dakota Sanford School of Medicine.
Background: Meningiomas and hemangioblastomas are two entities neurosurgeons may encounter in the posterior fossa. Each lesion has its own unique imaging findings, clinical presentation, and associated risks. Treatment for the two lesions may vary but surgical resection is typically considered definitive for both.
View Article and Find Full Text PDFSci Rep
August 2025
School of Medicine, Department of Neurosurgery, Johns Hopkins University, 600 N. Wolfe Street / Meyer 5-181, Baltimore, MD, 21287, USA.
Spinal cord hemangioblastomas are rare, benign, intradural tumors that, despite their nonmalignant histopathology, can lead to substantial neurological morbidity. While disparities in outcomes based on race and socioeconomic status have been well-documented in other spinal tumor populations, their role in spinal cord hemangioblastoma remains poorly understood. In this study, we utilize the National Cancer Database (NCDB) to evaluate the influence of race, socioeconomic factors, and healthcare access on survival outcomes in patients with spinal cord hemangioblastoma.
View Article and Find Full Text PDFEndoscopy
December 2025
Department of Gastroenterology, Qilu Hospital of Shandong University, Jinan, China.
J Neurosurg Case Lessons
August 2025
Department of Pediatrics, Division of Pediatric Hematology/Oncology, CHU de Québec-Université Laval, Québec City, Québec, Canada.
Background: Infantile hemangiomas (IHs) are the most common benign vascular tumors of infancy, although intracranial IHs remain exceedingly rare. Diagnosis is typically postnatal, with some cases requiring medical or surgical intervention. Here, the authors report the first case of a congenital cavernous sinus IH diagnosed via prenatal imaging and managed conservatively with successful spontaneous regression.
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