Abstract
Hypothalamic hamartoma is a rare congenital lesion. We present the case of a 7-year-old girl who suffered from precocious puberty, the cause of which was diagnosed by using MR imaging and CT as pedunculated hypothalamic hamartoma associated with a large craniopharyngeal canal and sellar spine mimicking pituitary duplication.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Child
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Diagnosis, Differential
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Female
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Hamartoma / congenital*
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Hamartoma / diagnosis
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Humans
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Hypothalamic Diseases / congenital*
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Hypothalamic Diseases / diagnosis
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Hypothalamus / pathology
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Image Enhancement*
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Image Processing, Computer-Assisted*
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Magnetic Resonance Imaging*
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Pituitary Gland / abnormalities
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Pituitary Gland / pathology
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Puberty, Precocious / etiology*
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Sella Turcica / abnormalities*
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Sella Turcica / pathology
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Skull Base / abnormalities*
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Skull Base / pathology
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Tomography, X-Ray Computed*