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scaly lesion with traces of irregularly distributed pigment&#44; surrounded by a diffuse&#44; vascularized erythematous area&#44; with some polymorphous-atypical vessels &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; There were no additional findings in the physical examination&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0020" class="elsevierStylePara elsevierViewall">The histopathology study showed an epidermis with focal ulceration&#44; parakeratosis&#44; and acanthosis with follicular induction&#46; A tumor was located in the dermis&#44; composed of spindle cells with vacuolated eosinophilic cytoplasm&#44; arranged in a storiform pattern&#44; embedded in a collagenous stroma with multiple foci of lamellar bone spicules but no osteoblasts or osteoclasts &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a>A and B&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What was the diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Dermatofibroma with metaplastic bone formation on the leg&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesions were completely excised and&#44; given their benign nature&#44; the surgical margins were not extended&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Remarks</span><p id="par0040" class="elsevierStylePara elsevierViewall">Dermatofibroma is a complex entity with a wide range of clinical&#44; dermoscopic&#44; and histopathologic features&#44; probably as a result of a series of as yet unknown triggers&#46; The case presented is the second report of a dermatofibroma with metaplastic bone formation without osteoclast-type giant cells&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a> Recognition in the histopathological study is very important&#44; as identification of metaplastic bone formation in the skin opens up a wide range of differential diagnoses&#44; from inflammatory-reactive processes to benign and malignant skin tumors&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Usually&#44; 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Findings include homogenous or irregular pigmentation&#44; multiple whitish patches&#44; whitish network&#44; coffee spots&#44; crusty scabs&#44; ulcers&#44; fissures&#44; irregular linear and polymorphic vessels&#44; and globular structures&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> Differential diagnosis is therefore usually broad and the lesions are sometimes difficult to distinguish from melanoma&#44; basal cell carcinoma and spindle cell carcinoma&#44; dermatofibrosarcoma protuberans&#44; Kaposi sarcoma&#44; morphea&#44; neurofibroma&#44; or adnexal tumor&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> In these cases&#44; surgical excision is necessary for pathology study to clarify diagnosis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">The key pathological findings are presence of a spindle-cell dermal tumor with fibrohistiocytic differentiation&#44; without atypia&#44; with trapped hyalinized collagen bundles in the periphery&#44; variable hemorrhage and hemosiderin deposition&#44; and epidermal changes &#40;acanthosis and follicular induction&#41;&#46; There are several histopathological variants according to the predominant microscopic component&#44; with fibrocollagenous&#44; histiocytic&#44; sclerotic&#44; cellular&#44; hemosiderotic&#44; and cobblestone subtypes&#44; among others&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> The presence of metaplastic bone formation in dermatofibroma is rare&#44; with few cases reported and no dermoscopic description of the lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">4&#8211;6</span></a> In general&#44; osteoclast-like giant cells are present&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The presence of bone tissue in the skin is uncommon&#44; and can be explained by a metaplastic process in response to trauma or local inflammatory processes&#46; The most common cutaneous tumors with metaplastic bone formation are melanocytic nevi&#44; basal cell carcinomas&#44; and pilomatrixomas&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">4</span></a> The presence of metaplastic bone tissue in the dermis and hypodermis may be a distraction during pathology study and mask the main lesion&#44; particularly when present in substantial amounts&#44; as in the case presented&#46; Metaplastic bone formation may correspond to the main component in certain tumors or be a process secondary to the main lesion&#46; Reactive processes with metaplastic bone tissue include scarring and panniculitis ossificans&#46; It is the main component of osteomas&#44; osteosarcomas&#44; ossifying fibromyxoid tumor&#44; and osteogenic melanoma&#44; or may be a secondary process in pilomatrixoma&#44; melanocytic nevi&#44; trichilemmal or pilar cysts&#44; and hemangiomas&#44; among others&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">5&#8211;7</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Long-standing Scaly Erythematous Tumor on the Lower Leg
Tumor eritemato-descamativo en la pierna de largo tiempo de evolución
A. Abarzúa-Arayaa, E. Ortiz-Lazoa,
Autor para correspondencia
eaortiz@uc.cl

Corresponding author.
, S. González-Bombardiereb
a Servicio de Dermatología, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
b Servicio de Anatomía Patológica, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Clinical Characteristics</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 36-year-old woman with no relevant personal history attended the clinic because of an asymptomatic lesion of 8 years duration on the left leg&#46; The lesion was growing slowly&#44; with constant scaling&#46; The patient could not recall any trigger associated with this lesion&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0010" class="elsevierStylePara elsevierViewall">The physical examination demonstrated the presence of a dome-shaped&#44; erythematous lesion of hard consistency with superficial scaling&#44; measuring 1&#46;5<span class="elsevierStyleHsp" style=""></span>cm&#44; on the anterior aspect of the left leg &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Figure 1</a>A and B&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Dermoscopy examination revealed a central whitish-yellow&#44; scaly lesion with traces of irregularly distributed pigment&#44; surrounded by a diffuse&#44; vascularized erythematous area&#44; with some polymorphous-atypical vessels &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Figure 2</a>&#41;&#46; There were no additional findings in the physical examination&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0020" class="elsevierStylePara elsevierViewall">The histopathology study showed an epidermis with focal ulceration&#44; parakeratosis&#44; and acanthosis with follicular induction&#46; A tumor was located in the dermis&#44; composed of spindle cells with vacuolated eosinophilic cytoplasm&#44; arranged in a storiform pattern&#44; embedded in a collagenous stroma with multiple foci of lamellar bone spicules but no osteoblasts or osteoclasts &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Figure 3</a>A and B&#41;&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What was the diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Dermatofibroma with metaplastic bone formation on the leg&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesions were completely excised and&#44; given their benign nature&#44; the surgical margins were not extended&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Remarks</span><p id="par0040" class="elsevierStylePara elsevierViewall">Dermatofibroma is a complex entity with a wide range of clinical&#44; dermoscopic&#44; and histopathologic features&#44; probably as a result of a series of as yet unknown triggers&#46; The case presented is the second report of a dermatofibroma with metaplastic bone formation without osteoclast-type giant cells&#46;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">1</span></a> Recognition in the histopathological study is very important&#44; as identification of metaplastic bone formation in the skin opens up a wide range of differential diagnoses&#44; from inflammatory-reactive processes to benign and malignant skin tumors&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Usually&#44; dermatofibromas present as a solid papule or nodule of red or coffee color with a smooth or keratotic surface&#46; The dimple sign can be observed with lateral compression&#44; but this is not exclusive to dermatofibroma and may not be very evident&#46; In the dermoscopy examination&#44; the most frequent pattern is a central white scar-like patch&#44; with a fine peripheral pigment network&#46;<a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">1&#8211;3</span></a> This pigmented network is not often distributed irregularly throughout the lesion &#40;2&#46;7&#37;&#41;&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> The presence of vascular structures has been reported in 50&#37; of cases&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">2&#44;3</span></a> Several dermoscopic findings and atypical patterns have been described&#46; These are uncommon and simulate other tumors&#46; Findings include homogenous or irregular pigmentation&#44; multiple whitish patches&#44; whitish network&#44; coffee spots&#44; crusty scabs&#44; ulcers&#44; fissures&#44; irregular linear and polymorphic vessels&#44; and globular structures&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">2</span></a> Differential diagnosis is therefore usually broad and the lesions are sometimes difficult to distinguish from melanoma&#44; basal cell carcinoma and spindle cell carcinoma&#44; dermatofibrosarcoma protuberans&#44; Kaposi sarcoma&#44; morphea&#44; neurofibroma&#44; or adnexal tumor&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> In these cases&#44; surgical excision is necessary for pathology study to clarify diagnosis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">The key pathological findings are presence of a spindle-cell dermal tumor with fibrohistiocytic differentiation&#44; without atypia&#44; with trapped hyalinized collagen bundles in the periphery&#44; variable hemorrhage and hemosiderin deposition&#44; and epidermal changes &#40;acanthosis and follicular induction&#41;&#46; There are several histopathological variants according to the predominant microscopic component&#44; with fibrocollagenous&#44; histiocytic&#44; sclerotic&#44; cellular&#44; hemosiderotic&#44; and cobblestone subtypes&#44; among others&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">3</span></a> The presence of metaplastic bone formation in dermatofibroma is rare&#44; with few cases reported and no dermoscopic description of the lesion&#46;<a class="elsevierStyleCrossRefs" href="#bib0055"><span class="elsevierStyleSup">4&#8211;6</span></a> In general&#44; osteoclast-like giant cells are present&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">The presence of bone tissue in the skin is uncommon&#44; and can be explained by a metaplastic process in response to trauma or local inflammatory processes&#46; The most common cutaneous tumors with metaplastic bone formation are melanocytic nevi&#44; basal cell carcinomas&#44; and pilomatrixomas&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">4</span></a> The presence of metaplastic bone tissue in the dermis and hypodermis may be a distraction during pathology study and mask the main lesion&#44; particularly when present in substantial amounts&#44; as in the case presented&#46; Metaplastic bone formation may correspond to the main component in certain tumors or be a process secondary to the main lesion&#46; Reactive processes with metaplastic bone tissue include scarring and panniculitis ossificans&#46; It is the main component of osteomas&#44; osteosarcomas&#44; ossifying fibromyxoid tumor&#44; and osteogenic melanoma&#44; or may be a secondary process in pilomatrixoma&#44; melanocytic nevi&#44; trichilemmal or pilar cysts&#44; and hemangiomas&#44; among others&#46;<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">5&#8211;7</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0060" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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