Spontaneous regression of an epidermoid cyst of the cavernous sinus
被引:10
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作者:
Yanamadala, Vijay
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Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Yanamadala, Vijay
[1
,2
]
Lin, Ning
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机构:
Harvard Univ, Sch Med, Boston, MA USA
Childrens Hosp Boston, Dept Neurosurg, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Lin, Ning
[2
,3
]
Walcott, Brian P.
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机构:
Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Harvard Univ, Sch Med, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Walcott, Brian P.
[1
,2
]
Baird, Lissa C.
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Oregon Hlth & Sci Univ, Dept Neurosurg, Portland, OR 97201 USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Baird, Lissa C.
[4
]
Smith, Edward R.
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机构:
Harvard Univ, Sch Med, Boston, MA USA
Childrens Hosp Boston, Dept Neurosurg, Boston, MA USAMassachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
Smith, Edward R.
[2
,3
]
机构:
[1] Massachusetts Gen Hosp, Dept Neurosurg, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA USA
[3] Childrens Hosp Boston, Dept Neurosurg, Boston, MA USA
[4] Oregon Hlth & Sci Univ, Dept Neurosurg, Portland, OR 97201 USA
Epidermoid cysts are rare lesions in the pediatric population. The natural history of epidermoids is usually that of slow growth, although rupture and cases of malignant transformation have been reported. Spontaneous regression of an intracranial epidermoid cyst has not previously been described to our knowledge. We present a 3-year-old boy who presented with severe vertigo. MRI was performed which revealed a 2 cm non-enhancing lesion in the right cavernous sinus. The lesion was T1-hypoinsense, T2-hyperintense, and with evidence of restricted diffusion, consistent with an epidermoid cyst. The patient was followed with annual MRI studies over the next 3 years, demonstrating progressive reduction in the size of the lesion over time, with complete resolution after 3 years. The child's symptoms also resolved during this period. Long-term follow-up imaging at 5 years showed no evident lesion. To our knowledge, this is the first report documenting spontaneous regression of an intracranial epidermoid cyst. While isolated, this finding demonstrates the potential for involution of epidermoids and lends support to the clinical practice of careful observation of these lesions, especially when located in areas associated with high potential surgical morbidity. Importantly, the novelty of this observation suggests a need for further study to better elucidate the underlying mechanism of this regression. (C) 2014 Elsevier Ltd. All rights reserved.