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Surgery was excluded because of the size of the lesion and it was decided to take a wait-and-see approach&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Dermatomyofibroma was first described in 1991 by H&#252;gel&#44; who used the name plaque fibromatosis&#44; but a year later Kamino proposed the term dermatomyofibroma&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is a rare benign skin tumor that predominantly affects women&#46; In the largest series&#44; published by Wentzel et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> the mean age of the patients was 30 years &#40;range&#44; 3 to 51 years&#41;&#46; Some cases have also been reported in men&#44; the majority during childhood&#59; the youngest patient to date has been an 11-month-old infant boy&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a> It is thought that in men the lesion may undergo spontaneous regression during puberty&#44; whereas&#44; in women&#44; it grows slowly under the influence of female hormones&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">From a clinical point of view&#44; the majority of cases present as a palpable plaque or nodule measuring 1 to 2<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; with a hyperpigmented or erythematous-yellowish surface&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> However&#44; lesions presenting as large linear plaques of 8<span class="elsevierStyleHsp" style=""></span>cm have been reported&#44; and even annular lesions of up to 13<span class="elsevierStyleHsp" style=""></span>cm in diameter&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#8211;6</span></a> The lesions typically arise on the upper part of the trunk&#44; shoulders&#44; axillas&#44; and anterior abdomen&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> and there is a characteristic predilection for the posterior cervical region in prepubertal children&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> In the series by Wentzel&#44; 1 lesion was observed in the popliteal fossa&#44; the same site as in our case&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Histology shows a proliferation of spindle-shaped cells in the reticular dermis&#46; The cells are arranged in fascicles that run parallel to the epidermal surface&#59; the skin appendages and epidermis are not affected&#46; The cells present a uniform appearance with abundant eosinophilic cytoplasm and an elongated nucleus&#44; with no atypia or mitoses&#46; The elastic fibers may be increased in number and may be fragmented&#46; Immunohistochemistry should be performed in all cases&#46; The cells are positive for vimentin and often for smooth muscle actin&#44; but are negative for protein S-100&#44; CD34&#44; factor XIIIa&#44; desmin&#44; and caldesmon&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The importance of this entity is its differentiation from other tumors formed of spindle-shaped cells&#44; such as dermatofibroma and dermatofibrosarcoma protuberans&#46; Dermatofibroma and&#44; in particular&#44; its plaque variant with an atrophic appearance or multiple clustered dermatofibromas&#44; can be similar to our case&#44; but the cells of dermatofibroma are positive for factor XIIIa&#46; Dermatofibrosarcoma protuberans has a storiform histologic pattern and immunohistochemistry is positive for CD34&#46; Other diagnoses that must be ruled out are plaque neurofibroma&#44; which is positive for S-100&#44; hypertrophic scar&#44; characterized by an absence of elastic fibers&#44; and piloleiomyoma&#44; which is positive for caldesmon and desmin&#46; In the literature we found a case of an unclassifiable myofibroblastic cell proliferation with clinical manifestations similar to those of our patient&#44; but with a more prolonged course and larger size of the lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7&#8211;10</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The treatment of choice is excision with adequate surgical margins&#46; No recurrences or distant metastases have been observed&#46; In lesions that have been partially excised or in which conservative management has been applied&#44; no evidence of progression of the lesion has been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">We have described an elderly male patient with a large linear dermatomyofibroma of recent onset in the popliteal fossa&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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        "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as&#58; Torres C&#44; Revert &#193;&#44; Terr&#225;dez L&#44; Jord&#225; E&#46; Dermatomiofibroma lineal&#46; Actas Dermosifiliogr&#46; 2016&#59;107&#58;787&#8211;789&#46;</p>"
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Case and Research Letters
Linear Dermatomyofibroma
Dermatomiofibroma lineal
C. Torresa,
Autor para correspondencia
catitorresan@gmail.com

Corresponding author.
, Á. Reverta, L. Terrádezb, E. Jordáa,c
a Servicio de Dermatología, Hospital Clínico Universitario de Valencia, Valencia, Spain
b Servicio de Anatomía Patológica, Hospital Clínico Universitario de Valencia, Valencia, Spain
c Departamento de Medicina, Universidad de Valencia, Valencia, Spain
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with a linear distribution and poorly defined borders &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; The patient did not report trauma and described discomfort on flexing the limb&#46; On a suspicion of morphea&#44; the lesion was biopsied&#46; In the mid and deep dermis there was a proliferation of spindle-shaped cells in interwoven bundles&#44; with a tendency to run parallel to the epidermal surface&#46; This proliferation was composed of cells with wavy&#44; elongated nuclei with a rounded outline&#44; no atypia&#44; and with a poorly defined cytoplasm &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Immunohistochemistry was positive for smooth muscle actin&#44; but the cells were negative for CD34&#44; muscle specific actin&#44; and factor XIIIa&#46; Staining with orcein showed increased numbers and fragmentation of the elastic fibers &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; Based on these findings we made a diagnosis of dermatomyofibroma&#46; Surgery was excluded because of the size of the lesion and it was decided to take a wait-and-see approach&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Dermatomyofibroma was first described in 1991 by H&#252;gel&#44; who used the name plaque fibromatosis&#44; but a year later Kamino proposed the term dermatomyofibroma&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">2</span></a> It is a rare benign skin tumor that predominantly affects women&#46; In the largest series&#44; published by Wentzel et al&#46;&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> the mean age of the patients was 30 years &#40;range&#44; 3 to 51 years&#41;&#46; Some cases have also been reported in men&#44; the majority during childhood&#59; the youngest patient to date has been an 11-month-old infant boy&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a> It is thought that in men the lesion may undergo spontaneous regression during puberty&#44; whereas&#44; in women&#44; it grows slowly under the influence of female hormones&#46;<a class="elsevierStyleCrossRefs" href="#bib0065"><span class="elsevierStyleSup">3&#44;4</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">From a clinical point of view&#44; the majority of cases present as a palpable plaque or nodule measuring 1 to 2<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; with a hyperpigmented or erythematous-yellowish surface&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> However&#44; lesions presenting as large linear plaques of 8<span class="elsevierStyleHsp" style=""></span>cm have been reported&#44; and even annular lesions of up to 13<span class="elsevierStyleHsp" style=""></span>cm in diameter&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">4&#8211;6</span></a> The lesions typically arise on the upper part of the trunk&#44; shoulders&#44; axillas&#44; and anterior abdomen&#44;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a> and there is a characteristic predilection for the posterior cervical region in prepubertal children&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">3</span></a> In the series by Wentzel&#44; 1 lesion was observed in the popliteal fossa&#44; the same site as in our case&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">Histology shows a proliferation of spindle-shaped cells in the reticular dermis&#46; The cells are arranged in fascicles that run parallel to the epidermal surface&#59; the skin appendages and epidermis are not affected&#46; The cells present a uniform appearance with abundant eosinophilic cytoplasm and an elongated nucleus&#44; with no atypia or mitoses&#46; The elastic fibers may be increased in number and may be fragmented&#46; Immunohistochemistry should be performed in all cases&#46; The cells are positive for vimentin and often for smooth muscle actin&#44; but are negative for protein S-100&#44; CD34&#44; factor XIIIa&#44; desmin&#44; and caldesmon&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">The importance of this entity is its differentiation from other tumors formed of spindle-shaped cells&#44; such as dermatofibroma and dermatofibrosarcoma protuberans&#46; Dermatofibroma and&#44; in particular&#44; its plaque variant with an atrophic appearance or multiple clustered dermatofibromas&#44; can be similar to our case&#44; but the cells of dermatofibroma are positive for factor XIIIa&#46; Dermatofibrosarcoma protuberans has a storiform histologic pattern and immunohistochemistry is positive for CD34&#46; Other diagnoses that must be ruled out are plaque neurofibroma&#44; which is positive for S-100&#44; hypertrophic scar&#44; characterized by an absence of elastic fibers&#44; and piloleiomyoma&#44; which is positive for caldesmon and desmin&#46; In the literature we found a case of an unclassifiable myofibroblastic cell proliferation with clinical manifestations similar to those of our patient&#44; but with a more prolonged course and larger size of the lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">1&#44;7&#8211;10</span></a></p><p id="par0035" class="elsevierStylePara elsevierViewall">The treatment of choice is excision with adequate surgical margins&#46; No recurrences or distant metastases have been observed&#46; In lesions that have been partially excised or in which conservative management has been applied&#44; no evidence of progression of the lesion has been reported&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">1</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">We have described an elderly male patient with a large linear dermatomyofibroma of recent onset in the popliteal fossa&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Conflicts of Interest</span><p id="par0045" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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