%0 Journal Article
%T Intraosseous Lipoma of the Sphenoid: A Case Study
%A Zygmunt Jamrozik
%A Grzegorz Rosiak
%A Biruta Kierdaszuk
%A Krzysztof Milczarek
%A Anna Kami¨½ska
%A Dorota Dziewulska
%A Antoni Krzeski
%J Case Reports in Neurological Medicine
%D 2013
%I Hindawi Publishing Corporation
%R 10.1155/2013/519341
%X Intraosseous lipoma is very rare, usually benign tumor of flat bones. However, the localization in skull bones is described in sporadic cases. The differential diagnosis includes end stage of infection, infarct lesions, intraosseous meningioma, angiolipoma, or myxofibrous tumors. We report a patient with intraosseous lipoma located in the sphenoid bone. The diagnosis was established due to the characteristic radiological features. According to the history of seizures, the lesion was removed via endoscopic endonasal approach. Histopathological examination showed adipocytes. The patient underwent control neuroimaging studies. 1. Introduction Intraosseous lipoma (IL) is a rarely diagnosed, usually benign tumor placed in the flat bones, hardly ever in the long bones. Most often reported localizations include calcaneus, rib, and frontal and basal skull [1¨C3]. Lipoma originates from mesenchymal tissue and might resemble other benign tumors. Incidence of sphenoid bone and sphenoid sinus lipoma seems to be very rare although precise epidemiological data are not known [4¨C6]. It has been postulated that intraosseous lipomas grow as a result of infarct, end stage of infection, fibrous dysplasia, fibro- and angiolipoma, or liposclerosing myxofibrous tumors (LSMFT). All those should be included in the differential diagnosis of the intraosseous lipoma. 2. Case Report A patient, 23-year-old woman, has been referred to neurological department by an ophthalmologist with suspected papilledema. Two weeks earlier, she suffered from the first generalized tonic-clonic seizure after unexpected sudden pain. Medical history includes 2 attacks of unconsciousness after acute pain. A CT scan revealed a hypodense mass with central calcifications within sphenoid sinus and clivus. Density of the hypodense portion of mass ranged from £¿30 to £¿90 Hounsfield units suggesting presence of fat which surrounded central, scattered calcifications. Multilobulated margins of the lesion were sharp and sclerotic suggesting nonaggressive growth (Figure 1). MR scans showed a sphenoclival mass hyperintense in both T1WI (SE) and T2WI (TSE) with sharp and thin margin of low signal intensity corresponding with sclerotic rim. Cortex of sella turcica and clivus were intact. Fat suppressed sequence confirmed fat containing lesion; incomplete signal suppression was due to central calcifications. The lesion showed no contrast enhancement (Figure 2). Upon findings in both imaging modalities, a diagnosis of intraosseous lipoma was made. Figure 1: Routine CT scan revealed intraosseous lipoma within the sphenoid
%U http://www.hindawi.com/journals/crinm/2013/519341/