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Letter to the Editor
Interhemispheric lipoma associated with agenesis of the corpus callosum
Lipoma interhemisférico asociado a agenesia del cuerpo calloso
P.E. Jiménez Caballero
Facultativo Especialista de Área, Neurología, Sección de Neurología, Hospital San Pedro de Alcántara, Cáceres, Spain
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Cranial CT scan&#58; hypodense image measuring 5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>3<span class="elsevierStyleHsp" style=""></span>cm in the area of the corpus callosum &#40;arrow&#41;&#46; It is surrounded by mural calcifications on both sides&#46; Its density is indicative of fat content&#46; Agenesis of the corpus callosum&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Intracranial lipomas are uncommon and benign congenital malformations that account for only 0&#46;03&#37; to 0&#46;08&#37; of all types of intracranial masses&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> They are usually located in the interhemispheric fissure&#44; especially in the corpus callosum&#46; Lipomas of the corpus callosum are frequently associated with other congenital malformations of that structure&#44; such as agenesis&#44; hypoplasia&#44; or hypertrophy&#46; Since half of all cases are asymptomatic&#44; they are only diagnosed based on incidental findings in neuroimaging studies&#46; In the remainder of the cases&#44; they are associated with neurological symptoms such as psychomotor retardation&#44; headache&#44; epilepsy&#44; and cerebral palsy&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Our patient was a 23-year-old woman with a history of migraine without aura&#46; Her gestation and birth were uneventful and psychomotor development was normal&#46; She did not suffer from any febrile seizures&#44; cranial trauma&#44; or central nervous system infections during childhood&#46; She had no family history of epilepsy or any other neurological disorders&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient visited the emergency department with symptoms of disorientation and buccofacial movements suggesting complex partial epileptic seizure&#46; Neurological examination was normal&#46; The cranial CT scan carried out in the emergency department &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41; showed absence of the corpus callosum and a hypodense homogeneous lesion in its location&#46; We observed curvilinear calcifications on both sides of the lesion&#46; Findings suggested agenesis of the corpus callosum with interhemispheric lipoma&#46; Treatment with valproic acid was prescribed&#46; The electroencephalogram showed epileptiform activity in the left temporo-parietal region&#46; Brain MRI &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41; showed that the entire corpus callosum from the genu to the splenium was occupied by tissue that was hyperintense on all sequences&#44; with the exception of the fat suppression sequence&#46; The sagittal sequence showed bands of tissue that may correspond to remnants of the normal corpus callosum located between the lipomatous areas&#46; We also observed slight dilation of the posterior horns of both lateral ventricles&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0020" class="elsevierStylePara elsevierViewall">The patient received several antiepileptic drugs in different combinations&#44; but seizure control was never achieved&#46; Since that time we have performed several routine brain MRI scans and the lesion has remained unchanged&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Lipoma of the corpus callosum is a congenital disorder which probably arises due to poor differentiation of the meningeal tissue&#46; Agenesis of the corpus callosum is a type of cerebral dysraphism in which the neural tube does not close properly&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">This disorder is usually accompanied by epilepsy&#44; which may manifest as either partial simple seizures or complex seizures&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> The origin of seizures is unknown&#44; but they could stem from an epileptogenic focus caused when the cerebral cortex is invaded by the collagenous capsule of the lipoma&#44; or from interhemispheric disconnection&#46;</p><p id="par0035" class="elsevierStylePara elsevierViewall">The appearance of the corpus callosum lipoma on the cranial CT scan is quite typical&#44; with the low attenuation seen only in adipose tissue&#46; In addition&#44; it is surrounded by bilateral&#44; rounded mural calcifications&#46; After administration of contrast&#44; the lesion showed no changes&#46; In the brain MRI the lesion presents characteristics of fatty tissue&#44; with a hyperintense signal in both T1- and T2-weighted studies&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> During complete agenesis of the corpus callosum&#44; the lateral ventricles are far apart and never converge&#46; They often have small frontal horns and disproportionally thick occipital horns &#40;colpocephaly&#41;&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Differential diagnosis must be performed with epidermoid cyst&#44; teratoma&#44; craniopharyngioma&#44; and epidermoid tumours&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> The cystic content of the craniopharyngioma may have a fat-like density&#44; but the appearance is complex with atypical calcifications&#46; Teratomas and dermoid cysts are usually heterogeneous because they contain other tissues in addition to fat&#46; Dermoid cysts are generally located in the cerebellopontine angle&#44; parahypophyseal region&#44; or the fourth ventricle&#46; The density of the lesion in the cranial CT scan is similar to that of cerebrospinal fluid&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Some cases of interhemispheric lipomas are associated with agenesis of the corpus callosum resulting from connatal infection with cytomegalovirus or X chromosome deletion&#44; although most are idiopathic&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Surgical treatment is not recommended except in cases of secondary hydrocephalus that require ventriculoperitoneal shunting&#46; Surgery is not advisable in other cases due to their abundant vascularisation&#44; capsule infiltration&#44; and adherence to adjacent tissue&#44; plus the fact that these tumours do not grow and often have few clinical consequences&#46; Even when surgery is performed&#44; epileptic seizures rarely cease&#46; Nevertheless&#44; other authors have had favourable results using microsurgery and a CO<span class="elsevierStyleInf">2</span> laser&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a></p></span>"
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ISSN: 21735808
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