2008, Number 4
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Gac Med Mex 2008; 144 (4)
Malformación de Arnold-Chiari tipo I, siringomielia, siringobulbia y atrapamiento del ventrículo IV
Carrillo-Esper R, Vázquez-Elizondo G, Gutiérrez-Delgado LG, Guevara-Arnal L, Méndez-Sánchez N
Language: Spanish
References: 18
Page: 351-354
PDF size: 100.83 Kb.
Text Extraction
Arnold-Chiari Malformation (ACM) was first described by Hans Chiari in 1890. Four types of this malformation are recognized, of those, type I is the most common among adults. It is caused by an elongation of the cerebellum into the conic projections that accompany the brain stem within the spinal channel. It is mostly congenital but “acquired” forms can be seen in the context of infections or posterior fossa tumors. Clinically, it can present as an asymptomatic finding, but it can produce brain stem compression. Syringomielia – cavitation of the brain stem central areas – is associated with MAC type I in 75 to 85% of cases. Clinical signs include pain, weakness, extremity parestesia. A shunt to the lateral ventricles can produce IV ventricle entrapment and is associated with cerebrospinal fluid blockage. We describe a case of MAC type I associated with the presence of syringomielia, syringobulbia and IV ventricle entrapment.
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