16 April 2019
: Case report
Radiologic Features with Pathologic Correlation of an Unusual Large Intraosseous Skull Cavernous Hemangioma
Rare disease
Alvaro Bravo-Martinez1ABEF*, Amanda P. Marrero-Gonzalez1F, Mohammad N. Suleiman-Suleiman2B, Juan C. Vicenty-Padilla3B, Elizabeth Trullenque-Martinez1ADEDOI: 10.12659/AJCR.913414
Am J Case Rep 2019; 20:525-530
Abstract
BACKGROUND: Intraosseous cavernous skull hemangiomas are rare benign vascular tumors that are usually found incidentally on imaging, with an asymptomatic and slow-growing course. We present a case in which the patient had a mass on her forehead for many years, which began to grow rapidly after head trauma. Imaging characteristics play a crucial role in the diagnosis and description of this disease, and in differentiating it from other more common calvarial lesions that may present with a similar clinical picture. Here, we report an unusual presentation of a large skull hemangioma and discuss the different radiologic imaging findings and pathologic correlations.
CASE REPORT: A 58-year-old female with history of a lump on her forehead since childhood, which began to grow rapidly after experiencing a closed-head injury. Due to its large size, she went on to seek further management. Radiologic images revealed a frontal skull lesion suggestive of an intraosseous hemangioma. She underwent embolization of the tumor, and 2 days later underwent bilateral frontal craniectomy and cranioplasty. Histopathologic findings confirmed this diagnosis.
CONCLUSIONS: Intraosseous skull hemangioma may be confidently diagnosed and differentiated from other skull lesions by its imaging characteristics. An accurate diagnosis is essential to selecting correct management and avoiding complications.
Keywords: Bone Neoplasms, Hemangioma, Cavernous, Skull, Head Injuries, Closed, Magnetic Resonance Imaging, Skull Neoplasms, Tomography, X-Ray Computed
In Press
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.947545
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946515
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.946523
Case report
Am J Case Rep In Press; DOI: 10.12659/AJCR.947489
Most Viewed Current Articles
21 Jun 2024 : Case report
98,085
DOI :10.12659/AJCR.944371
Am J Case Rep 2024; 25:e944371
07 Mar 2024 : Case report
52,814
DOI :10.12659/AJCR.943133
Am J Case Rep 2024; 25:e943133
20 Nov 2023 : Case report
33,151
DOI :10.12659/AJCR.941424
Am J Case Rep 2023; 24:e941424
18 Feb 2024 : Case report
23,669
DOI :10.12659/AJCR.943030
Am J Case Rep 2024; 25:e943030