TY - JOUR
T1 - Large capillary hemangioma of the temporal bone with a dural tail sign: A case report
AU - Yang, Guang
AU - LI, CHENGUANG
AU - CHEN, XIN
AU - LIU, YAOHUA
AU - HAN, DAYONG
AU - Gao, Xin
AU - KAWAMOTO, KEIJI
AU - Zhao, Shiguang
N1 - KAUST Repository Item: Exported on 2020-10-01
PY - 2014/5/13
Y1 - 2014/5/13
N2 - The present study reports a rare case of large capillary hemangioma of the temporal bone with a dural tail sign. A 57-year-old female presented with pulsatile tinnitus and episodic vertigo associated with a ten-year history of an intermittent faint headache. Magnetic resonance imaging revealed a mass in the right petrous bone, which was hypointense on T1-weighted images and heterogeneously hyperintense on T2-weighted images, and showed a dural tail sign following gadolinium administration. Pre-operatively, this tumor was believed to be a meningioma. During surgery, the vascular tumor was removed by a modified pterional approach. A histopathological examination indicated that the tumor was a capillary hemangioma. Although intraosseous capillary hemangiomas are rare, they most frequently affect the temporal bone. Hemangiomas of the temporal bone may mimic other more common basal tumors. The diagnosis is most often made during surgical resection. The dural tail sign is not specific for meningioma, as it also occurs in other intracranial or extracranial tumors. The treatment of intratemporal hemangiomas is complete surgical excision, with radiotherapy used for unresectable lesions. To the best of our knowledge, the present study is the fourth case of intraosseous intracranial capillary hemangioma, but the largest intratemporal hemangioma to be reported in the literature to date.
AB - The present study reports a rare case of large capillary hemangioma of the temporal bone with a dural tail sign. A 57-year-old female presented with pulsatile tinnitus and episodic vertigo associated with a ten-year history of an intermittent faint headache. Magnetic resonance imaging revealed a mass in the right petrous bone, which was hypointense on T1-weighted images and heterogeneously hyperintense on T2-weighted images, and showed a dural tail sign following gadolinium administration. Pre-operatively, this tumor was believed to be a meningioma. During surgery, the vascular tumor was removed by a modified pterional approach. A histopathological examination indicated that the tumor was a capillary hemangioma. Although intraosseous capillary hemangiomas are rare, they most frequently affect the temporal bone. Hemangiomas of the temporal bone may mimic other more common basal tumors. The diagnosis is most often made during surgical resection. The dural tail sign is not specific for meningioma, as it also occurs in other intracranial or extracranial tumors. The treatment of intratemporal hemangiomas is complete surgical excision, with radiotherapy used for unresectable lesions. To the best of our knowledge, the present study is the fourth case of intraosseous intracranial capillary hemangioma, but the largest intratemporal hemangioma to be reported in the literature to date.
UR - http://hdl.handle.net/10754/325366
UR - https://www.spandidos-publications.com/10.3892/ol.2014.2143
UR - http://www.scopus.com/inward/record.url?scp=84901194174&partnerID=8YFLogxK
U2 - 10.3892/ol.2014.2143
DO - 10.3892/ol.2014.2143
M3 - Article
C2 - 24959241
SN - 1792-1082
VL - 8
SP - 183
EP - 186
JO - Oncology Letters
JF - Oncology Letters
IS - 1
ER -