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arranged in a non-specific pattern in a myxoid stroma with extravasated blood cells and fibrous areas with hyalinized collagen &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a>&#44; hematoxylin-eosin&#44; original magnification<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>400&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Nodular fasciitis &#40;NF&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">NF was first described by Konwaler et al&#46; in 1954 as &#8220;subcutaneous pseudosarcomatous fibromatosis &#40;fasciitis&#41;&#46;&#8221;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> It is a fast-growing proliferative lesion that mainly affects the subcutaneous cellular tissue&#44; fascia&#44; and muscle&#44; although a rare dermal variant also exists&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The etiology and pathogenesis of NF remain uncertain&#44; although it is considered to be a reactive&#44; benign&#44; self-limiting process<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#8211;4</span></a> related&#44; in isolated cases&#44; to infectious processes or trauma&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> It usually appears in white men<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> in the third or fourth decades of life<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a>&#59; only 10&#37; of cases are found in children anywhere from several months to 18 years of age&#44; with the average age falling between 8 and 14 years&#44; depending on the case series&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#8211;5</span></a> The most common site of NF lesions is the extremities and trunk&#44; followed by the head and neck&#44; the most frequent site during childhood&#44;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#44;5</span></a> although reports of NF in children are rare&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#44;5</span></a> NF usually presents as a single asymptomatic lesion&#46; Clinically&#44; NF is characterized by a firm nodule&#44; either fixed or mobile&#44; that is generally less than 3<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; skin-colored or erythematous&#44; sometimes painful&#44; and without palpable lymph nodes&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;3&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">NF is diagnosed histopathologically&#46; Presurgical imaging studies help to better define the lesion and rule out other possible diagnoses&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologic examination shows a proliferation of fibroblasts and myofibroblasts with an increase in mitotic activity and loose myxoid stroma&#44;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> with increased vascularization&#44; extravasated erythrocytes&#44; chronic inflammatory infiltrate<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;4</span></a> and occasional osteoclastic giant cells&#46; Price et al&#46; were the first to classify NF in 3 histologic subtypes&#58; myxoid or reactive &#40;type <span class="elsevierStyleSmallCaps">i</span>&#44; the most common type&#41;&#44; cellular &#40;type <span class="elsevierStyleSmallCaps">ii</span>&#41;&#44; and fibrous &#40;type <span class="elsevierStyleSmallCaps">iii</span>&#41;&#46; It has been suggested that these subtypes may not be independent but rather that they represent the progression of NF over time&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> Immunohistochemical studies are positive for muscle-specific actin&#44; smooth muscle actin&#44; calponin&#44; and vimentin and negative for desmin&#44; cytokeratin&#44; h-caldesmon&#44; smooth muscle myosin&#44; S100 protein&#44; and CD34&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#44;5&#44;6</span></a> As in other mesenchymal tumors&#44; cytogenetic studies have revealed rearrangements of the USP6 locus related to high mitotic activity&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis includes benign lesions such as dermoid or epidermoid cysts&#44; pilomatricoma&#44; lipoma&#44; and postoperative or posttraumatic nodules&#44; as well as malignant tumors<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#8211;5</span></a> such as fibrosarcoma&#44; malignant peripheral nerve sheath tumor&#44; undifferentiated pleomorphic sarcoma&#44; and dermatofibrosarcoma protuberans&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Despite its reactive character and the possibility of spontaneous remission&#44; surgical excision appears to be the most reasonable form of management&#44; especially in children&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> Recurrences are rare and require that the diagnosis be reconsidered&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#8211;5</span></a></p></span></span>"
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Case for Diagnosis
Subcutaneous Tumor Deep to the Lateral Right Eyebrow
Tumoración subcutánea en la cola de la ceja derecha
P.P. García-Monteroa,
Autor para correspondencia
pablo.garcia.montero@gmail.com

Corresponding author.
, A. Hernández-Nuñeza, J.C. Tardíob
a Servicio de Dermatología, Hospital Universitario de Fuenlabrada, Madrid, Spain
b Servicio de Anatomía Patológica, Hospital Universitario de Fuenlabrada, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Medical History</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 12-year-old girl with no relevant past history presented with a lesion on the lateral portion of the right eyebrow that had appeared 2 months earlier&#46; The patient had no history of trauma&#46; She reported occasional pain and an increase in the size of the lesion&#44; followed by stabilization&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">Physical examination revealed an ill-defined oval-shaped subcutaneous growth measuring 2<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; with a firm elastic consistency&#44; adherent to the deeper tissues&#44; with no alterations of the underlying skin &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0015" class="elsevierStylePara elsevierViewall">Radiographs of the face&#44; orbit&#44; superior orbital fissure&#44; and skull were normal&#46; Soft-tissue ultrasound revealed a solid&#44; rounded growth with some small vessels in the subcutaneous cellular tissue &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Clinical Course and Treatment</span><p id="par0020" class="elsevierStylePara elsevierViewall">The lesion was completely excised&#44; and after 8 months of follow-up there were no signs of local recurrence and no other lesions had appeared&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Histopathology</span><p id="par0025" class="elsevierStylePara elsevierViewall">Histologic examination revealed a localized growth in the subcutaneous cellular tissue formed by a proliferation of multipolar spindle-shaped fibroblasts and myofibroblasts with vesicular nuclei and prominent nucleoli&#44; arranged in a non-specific pattern in a myxoid stroma with extravasated blood cells and fibrous areas with hyalinized collagen &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a>&#44; hematoxylin-eosin&#44; original magnification<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>400&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0030" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Diagnosis</span><p id="par0035" class="elsevierStylePara elsevierViewall">Nodular fasciitis &#40;NF&#41;&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">NF was first described by Konwaler et al&#46; in 1954 as &#8220;subcutaneous pseudosarcomatous fibromatosis &#40;fasciitis&#41;&#46;&#8221;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> It is a fast-growing proliferative lesion that mainly affects the subcutaneous cellular tissue&#44; fascia&#44; and muscle&#44; although a rare dermal variant also exists&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> The etiology and pathogenesis of NF remain uncertain&#44; although it is considered to be a reactive&#44; benign&#44; self-limiting process<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#8211;4</span></a> related&#44; in isolated cases&#44; to infectious processes or trauma&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> It usually appears in white men<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">3</span></a> in the third or fourth decades of life<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a>&#59; only 10&#37; of cases are found in children anywhere from several months to 18 years of age&#44; with the average age falling between 8 and 14 years&#44; depending on the case series&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#8211;5</span></a> The most common site of NF lesions is the extremities and trunk&#44; followed by the head and neck&#44; the most frequent site during childhood&#44;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#44;5</span></a> although reports of NF in children are rare&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#44;5</span></a> NF usually presents as a single asymptomatic lesion&#46; Clinically&#44; NF is characterized by a firm nodule&#44; either fixed or mobile&#44; that is generally less than 3<span class="elsevierStyleHsp" style=""></span>cm in diameter&#44; skin-colored or erythematous&#44; sometimes painful&#44; and without palpable lymph nodes&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#44;3&#44;4</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">NF is diagnosed histopathologically&#46; Presurgical imaging studies help to better define the lesion and rule out other possible diagnoses&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologic examination shows a proliferation of fibroblasts and myofibroblasts with an increase in mitotic activity and loose myxoid stroma&#44;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a> with increased vascularization&#44; extravasated erythrocytes&#44; chronic inflammatory infiltrate<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;4</span></a> and occasional osteoclastic giant cells&#46; Price et al&#46; were the first to classify NF in 3 histologic subtypes&#58; myxoid or reactive &#40;type <span class="elsevierStyleSmallCaps">i</span>&#44; the most common type&#41;&#44; cellular &#40;type <span class="elsevierStyleSmallCaps">ii</span>&#41;&#44; and fibrous &#40;type <span class="elsevierStyleSmallCaps">iii</span>&#41;&#46; It has been suggested that these subtypes may not be independent but rather that they represent the progression of NF over time&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> Immunohistochemical studies are positive for muscle-specific actin&#44; smooth muscle actin&#44; calponin&#44; and vimentin and negative for desmin&#44; cytokeratin&#44; h-caldesmon&#44; smooth muscle myosin&#44; S100 protein&#44; and CD34&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#44;5&#44;6</span></a> As in other mesenchymal tumors&#44; cytogenetic studies have revealed rearrangements of the USP6 locus related to high mitotic activity&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a></p><p id="par0055" class="elsevierStylePara elsevierViewall">The clinical differential diagnosis includes benign lesions such as dermoid or epidermoid cysts&#44; pilomatricoma&#44; lipoma&#44; and postoperative or posttraumatic nodules&#44; as well as malignant tumors<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#8211;5</span></a> such as fibrosarcoma&#44; malignant peripheral nerve sheath tumor&#44; undifferentiated pleomorphic sarcoma&#44; and dermatofibrosarcoma protuberans&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">Despite its reactive character and the possibility of spontaneous remission&#44; surgical excision appears to be the most reasonable form of management&#44; especially in children&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a> Recurrences are rare and require that the diagnosis be reconsidered&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#8211;5</span></a></p></span></span>"
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ISSN: 15782190
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