dc.creatorAlves, Crésio de Aragão Dantas
dc.creatorBarbosa, Veronica
dc.creatorMachado, Marcos
dc.creatorAlves, Crésio de Aragão Dantas
dc.creatorBarbosa, Veronica
dc.creatorMachado, Marcos
dc.date.accessioned2022-10-07T17:51:16Z
dc.date.available2022-10-07T17:51:16Z
dc.date.issued2013
dc.identifier0256-7040
dc.identifierhttp://www.repositorio.ufba.br/ri/handle/ri/12793
dc.identifierv. 29, n. 3
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4010577
dc.description.abstractIntroduction Hypothalamic hamartomas are very rare(1:200,000) and range in size from 17.9 to 18 mm. When their dimensions exceed 30–40 mm, they are classified as giant hypothalamic hamartomas. Methods We present a 14-month-old boy with central precocious puberty and gelastic seizures in whom a magnetic resonance imaging scan revealed a giant hypothalamic hamartoma measuring 50×50×40 mm. Results In the 11 cases described so far, we found that in comparison to the average-size lesion, giant hypothalamic hamartomas had a lower frequency of precocious puberty, but a similar frequency of seizures. The mean age at diagnosis was younger, and males were more affected than females. Magnetic resonance imaging results were similar with the exception of mass effect. Conclusions Giant hypothalamic hamartomas had a higher tendency to adhere to surrounding structures. Their invasiveness and cystic degeneration were frequent findings among the 11 studies. Surgical removal was ineffective in controlling refractory epilepsy and caused postoperative morbidity in all patients.
dc.languageen
dc.publisherChild's Nervous System
dc.source10.1007/s00381-013-2022-y
dc.subjectHypothalamic hamartomas
dc.subjectPrecocious puberty
dc.subjectGelastic seizures
dc.subjectGiant brain tumor
dc.titleGiant hypothalamic hamartoma: case report and literature review
dc.typeArtigo de Periódico


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