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Letter to the Editor
Comments on the published Letter to the Editor by Martínez-Lapiscina et al.: “Epileptic seizure and lipoma of the corpus callosum: Cause or finding”
Comentarios a la carta del editor publicada por Martínez-Lapiscina et al: «Crisis epiléptica y lipoma del cuerpo calloso: causa o hallazgo»
J.S. Lucena Romero
Corresponding author
joaquin.lucena@gmail.com

Corresponding author.
, M. Santos Rodríguez, A. Rico García, R. Marín Andrés, M.R. Blanco Rodríguez
Servicio de Patología Forense, Instituto de Medicina Legal, Sevilla, Spain
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Fresh coronal section of the brain at the level of the basal ganglia&#46; It is possible to observe an interhemispheric lipoma located in the anterior part of the corpus callosum&#46;</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">We read with great interest the recent article by Martinez-Lapiscina et al&#46;&#44; &#8220;Epileptic seizures and lipoma of the corpus callosum&#58; cause or finding&#8221;&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> As the authors demonstrate&#44; &#8220;intracranial lipomas can cause epileptic seizures and their correct diagnosis has prognostic and therapeutic implications&#8221;&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">Some years ago we published a case of lipoma of the corpus callosum in a 42-year-old male who died suddenly due to food aspiration as a result of an epileptic seizure while he was dining&#46; A neuropathological study revealed two curvilinear lipomas located at the top of the genu of the corpus callosum &#40;2&#46;5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>0&#46;7<span class="elsevierStyleHsp" style=""></span>cm and 1&#46;5<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>0&#46;5<span class="elsevierStyleHsp" style=""></span>cm&#44; respectively&#41;&#46; These consisted of mature adipose tissue and were very well vascularised&#46; They were not associated with developmental abnormalities of the corpus callosum&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">It is noteworthy that our patient had presented two previous seizures at 28 and 40 years of age&#44; so he had undergone EEG&#44; CT and MRI scans&#59; these showed &#8220;brain fat&#8221;&#44; as reported by the family &#40;we did not have access to medical records&#41;&#46; The patient was not following anticonvulsant therapy&#44; since no clinical indication was considered&#46; This fact was confirmed by a negative result in the chemical&#8211;toxicological analysis performed&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">Recently&#44; we had another case of lipoma of the corpus callosum as an incidental finding during the autopsy of a 41-year-old woman who died suddenly due to digestive pathology&#46; It was a tubulonodular lipoma measuring 2<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>4<span class="elsevierStyleHsp" style=""></span>cm&#44; of interhemispheric location&#44; situated in the anterior corpus callosum&#46; It was not associated to any dysgenesis or other neuronal migration abnormalities &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Although the patient had not presented epileptic seizures&#44; she had a history of headache and mild psychomotor retardation&#46; The facies was somewhat coarse&#44; with frontal prominence and low-set ears&#44; suggesting a defect in the development of the midline&#44; as other authors have mentioned&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#8211;5</span></a> Intracranial lipomas are rare congenital malformations&#44; representing only 0&#46;03&#8211;0&#46;08&#37; of all intracranial masses&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;3</span></a> In the past 6&#8211;1&#47;2 years&#44; we have performed a total of 6011 legal autopsies at our department and found only 2 exposed cases of lipomas of the corpus callosum &#40;an incidence of 0&#46;03&#37;&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">We completely agree with the view expressed by the authors when they mention that intracranial lipomas can cause epileptic seizures&#44; so a higher prevalence of lipomas should be considered in the epileptic population&#46; On the other hand&#44; anticonvulsant therapy may be necessary in these cases&#44; especially in symptomatic patients&#46;</p><p id="par0030" class="elsevierStylePara elsevierViewall">Finally&#44; we consider that&#44; in addition to diagnosing the cause of death&#44; a forensic pathologist is required to explain the pathophysiological mechanisms of the disease&#44; as well as any possible aetiologies and risk factors involved&#46; This is the philosophy that we attempt to apply during our daily work&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara">Please cite this article as&#58; Lucena Romero JS&#44; et al&#46; Comentarios a la carta del editor publicada por Mart&#237;nez-Lapiscina et al&#58; &#171;Crisis epil&#233;ptica y lipoma del cuerpo calloso&#58; causa o hallazgo&#187;&#46; Neurolog&#237;a&#46; 2011&#59;27&#58;57&#8211;8&#46;</p>"
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Article information
ISSN: 21735808
Original language: English
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