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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Precalcaneal congenital fibrolipomatous hamartoma &#40;PCFH&#41; is a rare and benign childhood skin disorder&#44; with only a few cases reported in the literature&#46; It has been referred to by a variety of names&#44; including pedal papules in the newborn&#44; congenital piezogenic-like papules&#44; and bilateral congenital adipose plantar nodules&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 9-month-old girl&#44; with no relevant personal or family history&#44; whose family brought her to consultation for the presence of symmetric subcutaneous nodular lesions on the plantar surface of both feet&#44; just anterior to the heels &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesions had been present since birth&#46; They had a soft consistency&#44; were poorly circumscribed&#44; and were not adherent to the superficial or deeper layers&#46; The overlying skin was normal&#46; They had a diameter of 1&#46;5&#160;cm at their widest point and appeared to be asymptomatic&#46; There were no other evident abnormalities&#46; Based on these clinical features&#44; a diagnosis of PCFH was made&#46; The lesions remained unchanged over more than 6 months of follow-up&#46; During this time&#44; the patient started to walk and there was no gait disturbance&#46; Treatment was not considered necessary&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">PCFH was first reported in 1990 by Larralde et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> who described the nodules as <span class="elsevierStyleItalic">pedal papules in the newborn</span>&#46; In 1996&#44; Larregue et al&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> called the disorder <span class="elsevierStyleItalic">precalcaneal congenital fibrolipomatous hamartoma</span> and this term has been used ever since&#46; The literature contains only isolated case reports and small series&#46; Although PCFH appears to be rare&#44; it is probably underdiagnosed because of low awareness among clinicians and the benign nature of the nodules&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">It is typically present at birth&#44; but it can develop later&#46; It has been reported to be slightly more common in males than in females&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Its pathogenesis is unknown&#46; Early descriptions suggested that it might be due to incomplete regression of fetal tissue<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a> as fibrolipomatous fetal tissue in the area of the heel exhibits physiologic hypodermic hypertrophy&#46; However&#44; the fact that fetal adipose tissue has never been detected on histologic examination and that a higher incidence of PCFH has not been noted in preterm infants would seem to contradict this theory&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> Other possible causes that have been suggested include a congenital alteration in the fibroconnective trabecular network of the adipose tissue<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#8211;10</span></a> and a tissue overgrowth disorder&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">PCFH tends to appear sporadically&#44; although there have been reports of a familial association&#44;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;6&#44;7&#44;9</span></a> with an apparently autosomal dominant pattern of inheritance&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7&#44;9</span></a> It has also been suggested that there might be an X-linked or mitochondrial inheritance pattern&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">PCFH is characterized by the presence of soft&#44; symmetric&#44; mobile&#44; subcutaneous nodular lesions that are generally located on the mid region of the soles of both feet&#44; just anterior to the heel&#44; although they can also extend onto the heel&#46; On occasions&#44; the nodules can be more prominent on one foot than on the other&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> The color of the overlying skin is normal&#46; The nodules are asymptomatic and have not been reported to cause gait disturbance&#46; Accordingly&#44; they do not generally require treatment&#44; but surgical excision is an option if they cause discomfort&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">The natural history of PCFH is not well established&#46; The nodules tend to increase in size as the child grows&#44; and there have been reports of lesions persisting well into adulthood&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> However&#44; because so few reports have been published on this relatively recently described disorder&#44; little is known about clinical course or potential for spontaneous regression&#46; There have been no reports to date of associated abnormalities or potential for malignant transformation&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology is generally not necessary to diagnose PCFH&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;10</span></a> Histologic findings include mature adipose tissue surrounded by collagen fibers of different thicknesses and normal elastic fibers&#46; In addition&#44; there may be mucin deposits at the periphery and within the fat lobules<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a> and an increased number of blood vessels without associated perivascular alterations&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> The above findings have been confirmed in ultrastructural studies&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The differential diagnosis should include piezogenic papules&#44; which are generally found in adults and are caused by herniation of fat through the dermis following injury&#46; Unlike PCHF nodules&#44; piezogenic papules are typically multiple and are often painful&#44; particularly on walking&#46; Other types of neonatal nodular lesions should also be considered in the differential diagnosis&#46; Examples are juvenile fibromatosis&#44; lipomas&#44; nevus lipomatosus&#44; dermal hypoplasia&#44; infantile hemangioma&#44; congenital hemangioma&#44; lymphatic malformation&#44; or plexiform neurofibroma&#44; all of which are typically unilateral&#46; In most cases&#44; these conditions can be distinguished by their clinical features&#46; In equivocal cases&#44; however&#44; histologic examination&#44; or even less invasive procedures such as transillumination or echo Doppler&#44; can be helpful&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">It is important to be familiar with this probably underdiagnosed disease and to inform parents that it is a harmless&#44; asymptomatic condition that is not associated with other abnormalities and generally does not require further tests or aggressive treatments&#46; Parents should also be informed that it might be hereditary&#44; although the pattern of transmission has not yet been well established&#46;</p></span>"
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Cases and Research Letters
Precalcaneal Congenital Fibrolipomatous Hamartoma
Hamartoma fibrolipomatoso precalcáneo congénito
C. Rubio-Flores
Autor para correspondencia
cristina.rubio.flores@gmail.com

Corresponding author.
, O. López-Barrantes González, C. Garrido-Gutiérrez, R.M. Díaz-Díaz
Sección de Dermatología, Hospital Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Precalcaneal congenital fibrolipomatous hamartoma &#40;PCFH&#41; is a rare and benign childhood skin disorder&#44; with only a few cases reported in the literature&#46; It has been referred to by a variety of names&#44; including pedal papules in the newborn&#44; congenital piezogenic-like papules&#44; and bilateral congenital adipose plantar nodules&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 9-month-old girl&#44; with no relevant personal or family history&#44; whose family brought her to consultation for the presence of symmetric subcutaneous nodular lesions on the plantar surface of both feet&#44; just anterior to the heels &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The lesions had been present since birth&#46; They had a soft consistency&#44; were poorly circumscribed&#44; and were not adherent to the superficial or deeper layers&#46; The overlying skin was normal&#46; They had a diameter of 1&#46;5&#160;cm at their widest point and appeared to be asymptomatic&#46; There were no other evident abnormalities&#46; Based on these clinical features&#44; a diagnosis of PCFH was made&#46; The lesions remained unchanged over more than 6 months of follow-up&#46; During this time&#44; the patient started to walk and there was no gait disturbance&#46; Treatment was not considered necessary&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">PCFH was first reported in 1990 by Larralde et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> who described the nodules as <span class="elsevierStyleItalic">pedal papules in the newborn</span>&#46; In 1996&#44; Larregue et al&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> called the disorder <span class="elsevierStyleItalic">precalcaneal congenital fibrolipomatous hamartoma</span> and this term has been used ever since&#46; The literature contains only isolated case reports and small series&#46; Although PCFH appears to be rare&#44; it is probably underdiagnosed because of low awareness among clinicians and the benign nature of the nodules&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">It is typically present at birth&#44; but it can develop later&#46; It has been reported to be slightly more common in males than in females&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">Its pathogenesis is unknown&#46; Early descriptions suggested that it might be due to incomplete regression of fetal tissue<a class="elsevierStyleCrossRefs" href="#bib0005"><span class="elsevierStyleSup">1&#8211;3</span></a> as fibrolipomatous fetal tissue in the area of the heel exhibits physiologic hypodermic hypertrophy&#46; However&#44; the fact that fetal adipose tissue has never been detected on histologic examination and that a higher incidence of PCFH has not been noted in preterm infants would seem to contradict this theory&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> Other possible causes that have been suggested include a congenital alteration in the fibroconnective trabecular network of the adipose tissue<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#8211;10</span></a> and a tissue overgrowth disorder&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">PCFH tends to appear sporadically&#44; although there have been reports of a familial association&#44;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;6&#44;7&#44;9</span></a> with an apparently autosomal dominant pattern of inheritance&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">7&#44;9</span></a> It has also been suggested that there might be an X-linked or mitochondrial inheritance pattern&#46;<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">PCFH is characterized by the presence of soft&#44; symmetric&#44; mobile&#44; subcutaneous nodular lesions that are generally located on the mid region of the soles of both feet&#44; just anterior to the heel&#44; although they can also extend onto the heel&#46; On occasions&#44; the nodules can be more prominent on one foot than on the other&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> The color of the overlying skin is normal&#46; The nodules are asymptomatic and have not been reported to cause gait disturbance&#46; Accordingly&#44; they do not generally require treatment&#44; but surgical excision is an option if they cause discomfort&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">The natural history of PCFH is not well established&#46; The nodules tend to increase in size as the child grows&#44; and there have been reports of lesions persisting well into adulthood&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#44;5</span></a> However&#44; because so few reports have been published on this relatively recently described disorder&#44; little is known about clinical course or potential for spontaneous regression&#46; There have been no reports to date of associated abnormalities or potential for malignant transformation&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Histology is generally not necessary to diagnose PCFH&#46;<a class="elsevierStyleCrossRefs" href="#bib0020"><span class="elsevierStyleSup">4&#8211;10</span></a> Histologic findings include mature adipose tissue surrounded by collagen fibers of different thicknesses and normal elastic fibers&#46; In addition&#44; there may be mucin deposits at the periphery and within the fat lobules<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#44;4</span></a> and an increased number of blood vessels without associated perivascular alterations&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> The above findings have been confirmed in ultrastructural studies&#46;<a class="elsevierStyleCrossRef" href="#bib0015"><span class="elsevierStyleSup">3</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">The differential diagnosis should include piezogenic papules&#44; which are generally found in adults and are caused by herniation of fat through the dermis following injury&#46; Unlike PCHF nodules&#44; piezogenic papules are typically multiple and are often painful&#44; particularly on walking&#46; Other types of neonatal nodular lesions should also be considered in the differential diagnosis&#46; Examples are juvenile fibromatosis&#44; lipomas&#44; nevus lipomatosus&#44; dermal hypoplasia&#44; infantile hemangioma&#44; congenital hemangioma&#44; lymphatic malformation&#44; or plexiform neurofibroma&#44; all of which are typically unilateral&#46; In most cases&#44; these conditions can be distinguished by their clinical features&#46; In equivocal cases&#44; however&#44; histologic examination&#44; or even less invasive procedures such as transillumination or echo Doppler&#44; can be helpful&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">It is important to be familiar with this probably underdiagnosed disease and to inform parents that it is a harmless&#44; asymptomatic condition that is not associated with other abnormalities and generally does not require further tests or aggressive treatments&#46; Parents should also be informed that it might be hereditary&#44; although the pattern of transmission has not yet been well established&#46;</p></span>"
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        "nota" => "<p class="elsevierStyleNotepara">Please cite this article as&#58; Rubio-Flores C&#44; L&#243;pez-Barrantes Gonz&#225;lez O&#44; Garrido-Guti&#233;rrez C&#44; D&#237;az-D&#237;az RM&#46; Hamartoma fibrolipomatoso precalc&#225;neo cong&#233;nito&#46; Actas Dermosifiliogr&#46;2012&#59;103&#58;651-653&#46;</p>"
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ISSN: 15782190
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2014 Julio 21 10 31
2014 Junio 29 6 35
2014 Mayo 33 7 40
2014 Abril 31 4 35
2014 Marzo 32 13 45
2014 Febrero 30 6 36
2014 Enero 24 9 33
2013 Diciembre 28 6 34
2013 Noviembre 19 6 25
2013 Octubre 11 7 18
2013 Septiembre 17 4 21
2013 Agosto 14 6 20
2013 Julio 11 3 14
2013 Junio 10 11 21
2013 Mayo 16 3 19
2013 Abril 16 12 28
2013 Marzo 14 7 21
2013 Febrero 24 3 27
2013 Enero 25 10 35
2012 Diciembre 15 5 20
2012 Octubre 1 6 7
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Idiomas
Actas Dermo-Sifiliográficas
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?