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   <subfield code="a">10.1007/s00381-007-0395-5</subfield>
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   <subfield code="a">Intramedullary cavernous angioma of the spinal cord in a pediatric patient, with multiple cavernomas, familial occurrence and partial spontaneous regression: case report and review of the literature</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Antonio Santoro, Manolo Piccirilli, Giacoma Brunetto, Roberto Delfini, Giampaolo Cantore]</subfield>
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   <subfield code="a">Object: The authors present their experience with the 17th pediatric intramedullary cavernoma reported in English literature. Methods: The patient firstly underwent surgery for a left frontal cavernoma when he was 2years old. Also the child's mother was operated for a C2-C3 intramedullary cavernoma. He grew up normally and the radiological follow-up was negative for other brainstem cavernous malformations. When he was 11years old he complained a worsening tetraparesis. A cerebral and spinal magnetic resonance (MR) imaging revealed the presence of a C1 intramedullary cavernoma and a pontine cavernoma. He underwent surgery for the cervical lesion, which was completely removed. The postoperative course was regular with a total recovery from the neurological deficit. The boy underwent a radiological follow-up, monitoring the pontine lesion, which spontaneously regressed when he was 19years old. Conclusion: The rarity of the pediatric intramedullary cavernoma, the familial occurrence, and the spontaneous regression of the pontine cavernoma make this case very peculiar.</subfield>
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   <subfield code="a">Intramedullary cavernous angioma</subfield>
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   <subfield code="a">Piccirilli</subfield>
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   <subfield code="a">Brunetto</subfield>
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   <subfield code="u">Department of Neurological Sciences-Neurosurgery, University of Rome &quot;La Sapienza”, Neurochirurgia1, Viale del Policlinico, 155, 00185, Rome, Italy</subfield>
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