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The diagnosis was congenital frontal lipoma&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient was lost to follow-up but returned when she was 8 months old&#46; A brain magnetic resonance imaging &#40;MRI&#41; study showed an interhemispheric hyperintense mass on both T1- and T2-weighted sequences and a hypointense mass on fat-suppressed T2-weighted images&#46; These findings were consistent with a lipoma &#40;1&#46;8<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>A-<span class="elsevierStyleHsp" style=""></span>0&#46;7<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>A-<span class="elsevierStyleHsp" style=""></span>0&#46;6<span class="elsevierStyleHsp" style=""></span>cm on the anteroposterior&#44; longitudinal&#44; and transverse planes&#44; respectively&#41; associated with hypoplasia of the splenium of the corpus callosum&#46; No tracts or other forms of communications were observed between the cerebral and frontal lipomas&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient was referred to a pediatric neurosurgeon&#44; who decided to keep her in clinical follow-up&#46; A second MRI study was performed 6 months later and no changes were observed &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was also referred to the otolaryngologist to rule out Pai syndrome&#59; the results of nasal fibroscopy were within normal limits&#46; A year after diagnosis&#44; the patient is still in follow-up&#44; with excellent developmental milestones and no evidence of neurological complications&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Although lipomas are the most common type of benign soft-tissue tumors in adults&#44; congenital presentation is rare&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Furthermore&#44; they are uncommon in children and account for just about 6&#37; of all soft-tissue tumors in pediatric patients&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Midline lipomas may be associated with central nervous system malformations&#44; and in such cases&#44; diverse radiologic studies and clinical follow-up are mandatory&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Intracranial lipomas are also rare&#44; accounting for just 0&#46;06Y&#95;&#34;0&#46;46&#37; of intracranial lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Most are located in the midline&#47;interhemispheric region&#44; most often in the corpus callosum&#46; In about 50&#37; of cases other disturbances&#44; frequently associated with varying degrees of hypoplasia or agenesis of the corpus callosum&#44; are identified in the surrounding nervous structures&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Subcutaneous lipomas in association with intracranial lipomas are even rarer&#46; The association could be related to the abnormal migration and proliferation of neural crest cells&#46; Abnormal neural crest development results in many craniofacial malformations&#44; known as neurocristopathies&#44; including facial midline clefts&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5Y&#95;&#34;7</span></a> Intracranial and extracranial lipomas may be independent entities or connected through a frontal bone defect on the skull&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Frontonasal dysplasia &#40;FND&#41; is a developmental alteration of the craniofacial region that comprises a spectrum of anomalies of the frontonasal area&#44; including hypertelorism&#44; nasal anomalies&#44; and&#47;or lip-palate cleft&#46; The exact origin of FND is unknown and most cases are sporadic&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> although a mutation in the <span class="elsevierStyleItalic">TGIF</span> gene has been observed in familial cases of FND&#44; which are very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Patients with FND may present with hypoplasia or agenesis of the corpus callosum and&#47;or a corpus callosum lipoma&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> In a case series of patients with FND&#44; all 8 patients had lipoma of the corpus callosum&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> Markers strongly associated with FND are falx cerebri calcifications and extracranial lipomas&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Midline lipomas of the face and other craniofacial anomalies may be associated with intracranial malformations&#44; including intracranial lipomas&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Brain MRI for the study of intracranial structures combined with clinical follow-up to monitor neurological changes seems to be the gold standard&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Pai syndrome should be included in the differential diagnosis of FND-spectrum anomalies&#46; This syndrome consists of pericallosal lipomas associated with facial abnormalities such as cutaneous polyps of the face and nasal mucosa&#44; midline cleft&#44; and midline pericallosal lipoma&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> As with our patient&#44; a nasal fibroscopy should be performed to rule out this syndrome&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Although the majority of patients with intracranial lipomas are asymptomatic&#44;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#44;11</span></a> a small number of patients may present neurological symptoms such as seizures&#44; headache&#44; and&#47;or behavioral or psychosocial disorders&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Routine neurosurgical treatment is not recommended because the surgical risk usually outweighs the benefits of the intervention&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Surgical resolution of extracranial lipoma may provide cosmetic improvement and better quality of life&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The prognosis and psychomotor development of patients with intracranial lipomas is not clear&#44; but based on data from patients with FND and Pai syndrome&#44; their prognosis would appear to be favorable&#44; with normal psychomotor development and no neurological impairment&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8-10</span></a> Some patients with FND may have psychological alterations such as misanthropy and shyness&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Lipomas are rare in children and are even rarer at birth&#46; Facial midline lipomas should be assessed by a multidisciplinary team consisting of a dermatologist&#44; neurosurgeons&#44; an otolaryngologist&#44; and radiologists&#46; Neurologic images should be taken and in cases associated with corpus callosum or pericallosal lipoma&#44; FND and Pai syndrome must be ruled out&#46; Whether our patient represents an isolated case of frontal congenital lipoma with associated cerebral lipoma or an incomplete case within the spectrum of FND is currently unknown&#46;</p></span>"
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Case and Research Letters
Frontal congenital lipoma and lipoma of the corpus callosum in an infant: A case report
Lipoma frontal congA(c)nito y lipoma del cuerpo calloso en un lactante: Informe de un caso
C. Navarrete-Dechenta, M. Curi-Tumab, M. Sandoval-Ossesa,
Autor para correspondencia
msandovalosses@yahoo.com

Corresponding author.
a Department of Dermatology, Facultad de Medicina, Pontificia Universidad CatA3lica de Chile, Santiago, Chile
b Facultad de Medicina, Pontificia Universidad CatA3lica de Chile, Santiago, Chile
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">An otherwise healthy 4-month-old girl who had been born full-term without birth trauma or prenatal or neonatal complications was brought to our practice because of a frontal tumor that had been present since birth&#46; Physical examination revealed a deep frontal tumor of medium consistency that was mobile&#44; unattached to the deeper layers&#44; and without epidermal changes &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The rest of the examination was normal&#46; No hypertelorism&#44; nasal alterations&#44; or dysmorphic facial features were observed&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">A soft-tissue cranial ultrasound performed when the infant was 2 days old showed slight thickening of the subcutaneous tissue&#59; this was also visible in a second ultrasound performed 2 months later&#46; The diagnosis was congenital frontal lipoma&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">The patient was lost to follow-up but returned when she was 8 months old&#46; A brain magnetic resonance imaging &#40;MRI&#41; study showed an interhemispheric hyperintense mass on both T1- and T2-weighted sequences and a hypointense mass on fat-suppressed T2-weighted images&#46; These findings were consistent with a lipoma &#40;1&#46;8<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>A-<span class="elsevierStyleHsp" style=""></span>0&#46;7<span class="elsevierStyleHsp" style=""></span>cm<span class="elsevierStyleHsp" style=""></span>A-<span class="elsevierStyleHsp" style=""></span>0&#46;6<span class="elsevierStyleHsp" style=""></span>cm on the anteroposterior&#44; longitudinal&#44; and transverse planes&#44; respectively&#41; associated with hypoplasia of the splenium of the corpus callosum&#46; No tracts or other forms of communications were observed between the cerebral and frontal lipomas&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">The patient was referred to a pediatric neurosurgeon&#44; who decided to keep her in clinical follow-up&#46; A second MRI study was performed 6 months later and no changes were observed &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; The patient was also referred to the otolaryngologist to rule out Pai syndrome&#59; the results of nasal fibroscopy were within normal limits&#46; A year after diagnosis&#44; the patient is still in follow-up&#44; with excellent developmental milestones and no evidence of neurological complications&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall">Although lipomas are the most common type of benign soft-tissue tumors in adults&#44; congenital presentation is rare&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Furthermore&#44; they are uncommon in children and account for just about 6&#37; of all soft-tissue tumors in pediatric patients&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Midline lipomas may be associated with central nervous system malformations&#44; and in such cases&#44; diverse radiologic studies and clinical follow-up are mandatory&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Intracranial lipomas are also rare&#44; accounting for just 0&#46;06Y&#95;&#34;0&#46;46&#37; of intracranial lesions&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a> Most are located in the midline&#47;interhemispheric region&#44; most often in the corpus callosum&#46; In about 50&#37; of cases other disturbances&#44; frequently associated with varying degrees of hypoplasia or agenesis of the corpus callosum&#44; are identified in the surrounding nervous structures&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">Subcutaneous lipomas in association with intracranial lipomas are even rarer&#46; The association could be related to the abnormal migration and proliferation of neural crest cells&#46; Abnormal neural crest development results in many craniofacial malformations&#44; known as neurocristopathies&#44; including facial midline clefts&#46;<a class="elsevierStyleCrossRefs" href="#bib0025"><span class="elsevierStyleSup">5Y&#95;&#34;7</span></a> Intracranial and extracranial lipomas may be independent entities or connected through a frontal bone defect on the skull&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;6</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">Frontonasal dysplasia &#40;FND&#41; is a developmental alteration of the craniofacial region that comprises a spectrum of anomalies of the frontonasal area&#44; including hypertelorism&#44; nasal anomalies&#44; and&#47;or lip-palate cleft&#46; The exact origin of FND is unknown and most cases are sporadic&#44;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> although a mutation in the <span class="elsevierStyleItalic">TGIF</span> gene has been observed in familial cases of FND&#44; which are very rare&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">Patients with FND may present with hypoplasia or agenesis of the corpus callosum and&#47;or a corpus callosum lipoma&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> In a case series of patients with FND&#44; all 8 patients had lipoma of the corpus callosum&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> Markers strongly associated with FND are falx cerebri calcifications and extracranial lipomas&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Midline lipomas of the face and other craniofacial anomalies may be associated with intracranial malformations&#44; including intracranial lipomas&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Brain MRI for the study of intracranial structures combined with clinical follow-up to monitor neurological changes seems to be the gold standard&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">Pai syndrome should be included in the differential diagnosis of FND-spectrum anomalies&#46; This syndrome consists of pericallosal lipomas associated with facial abnormalities such as cutaneous polyps of the face and nasal mucosa&#44; midline cleft&#44; and midline pericallosal lipoma&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> As with our patient&#44; a nasal fibroscopy should be performed to rule out this syndrome&#46;</p><p id="par0065" class="elsevierStylePara elsevierViewall">Although the majority of patients with intracranial lipomas are asymptomatic&#44;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">10&#44;11</span></a> a small number of patients may present neurological symptoms such as seizures&#44; headache&#44; and&#47;or behavioral or psychosocial disorders&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Routine neurosurgical treatment is not recommended because the surgical risk usually outweighs the benefits of the intervention&#46;<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> Surgical resolution of extracranial lipoma may provide cosmetic improvement and better quality of life&#46;</p><p id="par0070" class="elsevierStylePara elsevierViewall">The prognosis and psychomotor development of patients with intracranial lipomas is not clear&#44; but based on data from patients with FND and Pai syndrome&#44; their prognosis would appear to be favorable&#44; with normal psychomotor development and no neurological impairment&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8-10</span></a> Some patients with FND may have psychological alterations such as misanthropy and shyness&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">8&#44;9</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Lipomas are rare in children and are even rarer at birth&#46; Facial midline lipomas should be assessed by a multidisciplinary team consisting of a dermatologist&#44; neurosurgeons&#44; an otolaryngologist&#44; and radiologists&#46; Neurologic images should be taken and in cases associated with corpus callosum or pericallosal lipoma&#44; FND and Pai syndrome must be ruled out&#46; Whether our patient represents an isolated case of frontal congenital lipoma with associated cerebral lipoma or an incomplete case within the spectrum of FND is currently unknown&#46;</p></span>"
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