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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 40-year-old man was referred by the oncology department for assessment of pigmented lesions on the upper limbs that had appeared progressively over the previous 5 years&#46; The patient&#39;s medical history included a cholangiocarcinoma diagnosed 2 years earlier&#44; which was treated with surgery&#44; radiation therapy&#44; chemotherapy&#44; and oral capecitabine&#46; The patient was disease-free at the time of the visit&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The patient reported that the lesions had been stable and asymptomatic since they appeared&#44; that they did not change in appearance when exposed to high temperatures or physical exercise&#44; and that they did not change after treatment with topical antifungal agents prescribed by a primary care physician&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination revealed multiple well-defined brownish macules with fine superficial telangiectasias&#44; distributed in a bilateral symmetric pattern on the external aspect of both arms &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; The lesions were negative for the Darier sign&#46; No similar lesions were observed elsewhere on the body&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Biopsy of a lesion revealed basal layer hyperpigmentation and no other findings of interest &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; No increase in the number of mast cells or melanocytes was observed with hematoxylin-eosin staining or with immunostaining for c-kit&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Acquired bilateral telangiectatic macules&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesions have remained stable after 1 year of follow-up&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Acquired bilateral telangiectatic macules are a recently described entity&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The lesions have certain constant clinical and pathological characteristics that allow them to be differentiated from similar entities&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The lesions typically occur in middle-aged men with skin phototype <span class="elsevierStyleSmallCaps">III-IV</span><a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> and follow an insidious clinical course&#46; Patients present with symmetrically distributed brownish erythematous macules with fine superficial telangiectasias on the extensor surface of the arms&#46; The lesions are asymptomatic and negative for the Darier sign&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologic examination of the lesions reveals basal layer hyperpigmentation and capillary proliferation in the dermis&#44; sometimes accompanied by a subtle perivascular inflammatory infiltrate&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> No epidermal alterations are present and the number of mast cells and melanocytes is normal &#40;as can be confirmed by immunohistochemistry for c-kit and Fontana-Masson staining&#44; respectively&#41;&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">In the case series described by Park et al&#46;&#44; the lesions did not improve spontaneously in any of the patients after a mean follow-up period of 4 years&#46; In the case of our patient&#44; we did not prescribe treatment because the lesions were asymptomatic and stable&#46; No significant changes were observed during 14 months of follow-up&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">The differential diagnosis includes the following&#58;<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">&#8722;</span><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Telangiectasia macularis eruptiva perstans</span><a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a><span class="elsevierStyleItalic">&#58;</span> Indolent cutaneous mastocytosis characterized by brownish erythematous macules that are generally asymptomatic&#46; The lesions tend to be negative for the Darier sign&#46; Unlike acquired bilateral telangiectatic macules&#44; this entity also tends to affect the trunk&#46; Histologically&#44; it is characterized by an increase in the number of mast cells&#46;</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">&#8722;</span><p id="par0070" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Acquired brachial cutaneous dyschromatosis</span><a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a><span class="elsevierStyleItalic">&#58;</span> This recently described entity affects postmenopausal women and is characterized by greyish-brown asymptomatic macules on the extensor surface of the arms&#46; Histologically&#44; it is characterized by epidermal atrophy&#44; basal layer hyperpigmentation&#44; and solar elastosis&#46; Its appearance has been associated with UV radiation and the ingestion of angiotensin-converting enzyme inhibitors&#46;</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">&#8722;</span><p id="par0075" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Generalized essential telangiectasia</span><a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a><span class="elsevierStyleItalic">&#58;</span> This entity typically occurs in women 40 to 50 years of age&#46; It manifests as asymptomatic telangiectasias on the lower limbs that subsequently become generalized and is not associated with systemic diseases&#46;</p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">&#8722;</span><p id="par0080" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Hereditary benign telangiectasia</span><a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleItalic">&#58;</span> This rare entity is more frequent in women and children and is characterized by punctate telangiectasias surrounded by a pale halo on the upper third of the trunk&#44; the arms&#44; and the head&#46; The lesions are asymptomatic and are not associated with systemic disease&#46;</p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">&#8722;</span><p id="par0085" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Drug-induced hyperpigmentation&#58;</span> Various drugs&#8212;including antimalarial agents&#44; chemotherapeutic agents&#44; antibiotics&#44; amiodarone&#44; phenytoin&#44; and heavy metals&#8212;have been associated with pigmentary alterations&#46; In order to diagnose this entity&#44; a good medical history must be taken and a temporal relationship must be established between the administration of the drug and the appearance of the lesions&#46;</p></li></ul></p><p id="par0090" class="elsevierStylePara elsevierViewall">Therefore&#44; differences in sex and age at onset&#44; the absence of systemic symptoms&#44; the site of the lesions&#44; and histologic findings allow us to rule out other diseases and confirm the diagnosis of acquired bilateral telangiectatic macules&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have presented a new case of acquired bilateral telangiectatic macules&#44; a recently described entity characterized by asymptomatic pigmented lesions on the arms that occurs in grown men and follows a chronic indolent clinical course&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0100" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Hyperpigmented Macules on a Young Man's Arms
Máculas hiperpigmentadas bilaterales en brazos de un varón joven
S. de Asís-Cuestasa,
Autor para correspondencia
aifosofia00@gmail.com

Corresponding author.
, E. Martí-Iborb, A. Mateu-Puchadesa
a Servicio de Dermatología, Hospital Universitario Doctor Peset, Valencia, Spain
b Servicio de Anatomía Patológica, Hospital Universitario Doctor Peset, Valencia, 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 40-year-old man was referred by the oncology department for assessment of pigmented lesions on the upper limbs that had appeared progressively over the previous 5 years&#46; The patient&#39;s medical history included a cholangiocarcinoma diagnosed 2 years earlier&#44; which was treated with surgery&#44; radiation therapy&#44; chemotherapy&#44; and oral capecitabine&#46; The patient was disease-free at the time of the visit&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">The patient reported that the lesions had been stable and asymptomatic since they appeared&#44; that they did not change in appearance when exposed to high temperatures or physical exercise&#44; and that they did not change after treatment with topical antifungal agents prescribed by a primary care physician&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Physical Examination</span><p id="par0015" class="elsevierStylePara elsevierViewall">Physical examination revealed multiple well-defined brownish macules with fine superficial telangiectasias&#44; distributed in a bilateral symmetric pattern on the external aspect of both arms &#40;<a class="elsevierStyleCrossRefs" href="#fig0005">Figs&#46; 1 and 2</a>&#41;&#46; The lesions were negative for the Darier sign&#46; No similar lesions were observed elsewhere on the body&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Additional Tests</span><p id="par0020" class="elsevierStylePara elsevierViewall">Biopsy of a lesion revealed basal layer hyperpigmentation and no other findings of interest &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; No increase in the number of mast cells or melanocytes was observed with hematoxylin-eosin staining or with immunostaining for c-kit&#46;</p><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0025" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleBold">What Is Your Diagnosis&#63;</span></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Diagnosis</span><p id="par0030" class="elsevierStylePara elsevierViewall">Acquired bilateral telangiectatic macules&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course</span><p id="par0035" class="elsevierStylePara elsevierViewall">The lesions have remained stable after 1 year of follow-up&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Acquired bilateral telangiectatic macules are a recently described entity&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> The lesions have certain constant clinical and pathological characteristics that allow them to be differentiated from similar entities&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">The lesions typically occur in middle-aged men with skin phototype <span class="elsevierStyleSmallCaps">III-IV</span><a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> and follow an insidious clinical course&#46; Patients present with symmetrically distributed brownish erythematous macules with fine superficial telangiectasias on the extensor surface of the arms&#46; The lesions are asymptomatic and negative for the Darier sign&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Histologic examination of the lesions reveals basal layer hyperpigmentation and capillary proliferation in the dermis&#44; sometimes accompanied by a subtle perivascular inflammatory infiltrate&#46;<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> No epidermal alterations are present and the number of mast cells and melanocytes is normal &#40;as can be confirmed by immunohistochemistry for c-kit and Fontana-Masson staining&#44; respectively&#41;&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">In the case series described by Park et al&#46;&#44; the lesions did not improve spontaneously in any of the patients after a mean follow-up period of 4 years&#46; In the case of our patient&#44; we did not prescribe treatment because the lesions were asymptomatic and stable&#46; No significant changes were observed during 14 months of follow-up&#46;</p><p id="par0060" class="elsevierStylePara elsevierViewall">The differential diagnosis includes the following&#58;<ul class="elsevierStyleList" id="lis0005"><li class="elsevierStyleListItem" id="lsti0005"><span class="elsevierStyleLabel">&#8722;</span><p id="par0065" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Telangiectasia macularis eruptiva perstans</span><a class="elsevierStyleCrossRefs" href="#bib0040"><span class="elsevierStyleSup">2&#44;3</span></a><span class="elsevierStyleItalic">&#58;</span> Indolent cutaneous mastocytosis characterized by brownish erythematous macules that are generally asymptomatic&#46; The lesions tend to be negative for the Darier sign&#46; Unlike acquired bilateral telangiectatic macules&#44; this entity also tends to affect the trunk&#46; Histologically&#44; it is characterized by an increase in the number of mast cells&#46;</p></li><li class="elsevierStyleListItem" id="lsti0010"><span class="elsevierStyleLabel">&#8722;</span><p id="par0070" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Acquired brachial cutaneous dyschromatosis</span><a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">4</span></a><span class="elsevierStyleItalic">&#58;</span> This recently described entity affects postmenopausal women and is characterized by greyish-brown asymptomatic macules on the extensor surface of the arms&#46; Histologically&#44; it is characterized by epidermal atrophy&#44; basal layer hyperpigmentation&#44; and solar elastosis&#46; Its appearance has been associated with UV radiation and the ingestion of angiotensin-converting enzyme inhibitors&#46;</p></li><li class="elsevierStyleListItem" id="lsti0015"><span class="elsevierStyleLabel">&#8722;</span><p id="par0075" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Generalized essential telangiectasia</span><a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">5</span></a><span class="elsevierStyleItalic">&#58;</span> This entity typically occurs in women 40 to 50 years of age&#46; It manifests as asymptomatic telangiectasias on the lower limbs that subsequently become generalized and is not associated with systemic diseases&#46;</p></li><li class="elsevierStyleListItem" id="lsti0020"><span class="elsevierStyleLabel">&#8722;</span><p id="par0080" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Hereditary benign telangiectasia</span><a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">6</span></a><span class="elsevierStyleItalic">&#58;</span> This rare entity is more frequent in women and children and is characterized by punctate telangiectasias surrounded by a pale halo on the upper third of the trunk&#44; the arms&#44; and the head&#46; The lesions are asymptomatic and are not associated with systemic disease&#46;</p></li><li class="elsevierStyleListItem" id="lsti0025"><span class="elsevierStyleLabel">&#8722;</span><p id="par0085" class="elsevierStylePara elsevierViewall"><span class="elsevierStyleItalic">Drug-induced hyperpigmentation&#58;</span> Various drugs&#8212;including antimalarial agents&#44; chemotherapeutic agents&#44; antibiotics&#44; amiodarone&#44; phenytoin&#44; and heavy metals&#8212;have been associated with pigmentary alterations&#46; In order to diagnose this entity&#44; a good medical history must be taken and a temporal relationship must be established between the administration of the drug and the appearance of the lesions&#46;</p></li></ul></p><p id="par0090" class="elsevierStylePara elsevierViewall">Therefore&#44; differences in sex and age at onset&#44; the absence of systemic symptoms&#44; the site of the lesions&#44; and histologic findings allow us to rule out other diseases and confirm the diagnosis of acquired bilateral telangiectatic macules&#46;</p><p id="par0095" class="elsevierStylePara elsevierViewall">In conclusion&#44; we have presented a new case of acquired bilateral telangiectatic macules&#44; a recently described entity characterized by asymptomatic pigmented lesions on the arms that occurs in grown men and follows a chronic indolent clinical course&#46;</p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0100" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Información del artículo
ISSN: 15782190
Idioma original: Inglés
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