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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Case Description</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 56-year-old man with no relevant past history presented with mildly pruritic lesions on the dorsal aspect of both forearms that had first appeared 8 months earlier&#46; The patient reported no history of applying products to the affected area and mentioned no possible triggers&#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 large erythematous plaques with slightly raised borders and a central depression affecting the dorsal aspect of both forearms and hands&#46; The lesions had an annular morphology and&#44; interestingly&#44; spared the area covered by the watch on the left wrist &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Epicutaneous tests from the standard series of the Spanish Contact Dermatitis and Skin Allergy Research Group &#40;GEIDAC&#41; and standard photopatch tests were negative&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0020" class="elsevierStylePara elsevierViewall">Histologic examination of a punch biopsy specimen taken from the border of one of the plaques revealed an epidermis without significant alterations&#46; A superficial granulomatous and perivascular infiltrate composed of mononuclear cells and multinucleated giant cells was observed in the upper and mid dermis&#46; The cytoplasm of these cells contained numerous fragmented elastic fibers rendered more visible by Verhoeff-Van Gieson staining&#46; Neither collagen degeneration nor the presence of mucin were observed &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></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">Annular elastolytic giant cell granuloma &#40;actinic granuloma&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment was started with medium-strength topical corticosteroids and sun protection&#46; Partial improvement of the lesions was observed after 3 months of application&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Annular elastolytic giant cell granuloma &#40;AEGCG&#41;&#44; also known as actinic granuloma or O&#8217;Brien granuloma&#44; is a rare granulomatous disease characterized by the presence of multinucleated giant cells with phagocytosis of anomalous elastic fibers&#44; a process known as elastophagocytosis&#46; AEGCG mainly affects women aged 50 to 70 years with a light skin phototype and signs of chronic actinic damage&#46; The lesions usually begin as erythematous papules that later evolve into annular plaques with raised borders and a minimal atrophic center&#46; The most common sites are sun-exposed areas such as the face&#44; upper chest&#44; and legs&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The pathogenesis of this entity is unknown&#44; although the possibility of an autoimmune reaction directed against elastic fibers&#44; determining a granulomatous inflammatory response with the formation of granulomas&#44; has been postulated&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a> AEGCG has been described in association with various processes&#44; including diabetes mellitus&#44; medication use&#44; hypothyroidism&#44; thyroiditis&#44; lymphomas&#44; polymyalgia rheumatica&#44; and temporal arteritis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">At present&#44; it is not known whether there is a relationship between AEGCG and these processes&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Histopathology shows 3 well-defined zones that reflect this possible pathogenesis&#46; A peripheral zone&#44; outside the borders of the plaques&#44; is characterized by a papillary dermis with actinic elastosis&#44; without the presence of multinucleated giant cells or granulomas&#46; This zone&#44; in which the lesion progresses&#44; contains antigenic elastic fibers that have not yet induced an inflammatory reaction&#46; In an intermediate or active zone&#8212;corresponding clinically to the edge of the lesions&#8212;fragmented elastic fibers&#44; elastophagocytosis phenomena&#44; and granuloma formation are observed&#46; Finally&#44; a central zone&#44; characterized by the absence of elastic fibers and few inflammatory cells&#44; is the residual postinflammatory zone&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">3</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The main differential diagnosis is granuloma annulare &#40;GA&#41; at sun-exposed sites&#46; In fact&#44; since AEGCG was first described&#44; there has been some debate about whether it is a distinct entity or a variant of GA with elastophagocytosis&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a> Although these two processes can be clinically identical&#44; histologic studies support the idea that they are separate entities&#46; In AEGCG&#44; the granulomatous reaction is found mainly in the upper dermis and no mucin is observed&#44; whereas in GA&#44; granulomas are distributed throughout the upper and mid dermis&#44; forming a palisade around an area characterized by degenerated collagen and the presence of mucin&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">5</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Although spontaneous remission has been reported in some cases&#44; AEGCG tends to be chronic and recurring&#46; Multiple treatment options have been described&#44; including sun protection&#59; topical&#44; systemic&#44; or intralesional corticosteroids&#59; chloroquine&#59; dapsone&#59; methotrexate&#59; anti&#8211;tumor necrosis factor &#40;TNF&#41; monoclonal antibodies&#59; and low-dose oral retinoids&#46; These treatments have produced variable results&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">6&#8211;8</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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Case for Diagnosis
Bilateral Annular Plaques on the Hands and Forearms
Placas anulares bilaterales en manos y antebrazos
E. Rozas-Muñoz
Autor para correspondencia
docrozas@yahoo.com

Corresponding author.
, J.F. Mir-Bonafé, E. Serra-Baldrich
Servicio de Dermatología, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Case Description</span><p id="par0005" class="elsevierStylePara elsevierViewall">A 56-year-old man with no relevant past history presented with mildly pruritic lesions on the dorsal aspect of both forearms that had first appeared 8 months earlier&#46; The patient reported no history of applying products to the affected area and mentioned no possible triggers&#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 large erythematous plaques with slightly raised borders and a central depression affecting the dorsal aspect of both forearms and hands&#46; The lesions had an annular morphology and&#44; interestingly&#44; spared the area covered by the watch on the left wrist &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Epicutaneous tests from the standard series of the Spanish Contact Dermatitis and Skin Allergy Research Group &#40;GEIDAC&#41; and standard photopatch tests were negative&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Histopathology</span><p id="par0020" class="elsevierStylePara elsevierViewall">Histologic examination of a punch biopsy specimen taken from the border of one of the plaques revealed an epidermis without significant alterations&#46; A superficial granulomatous and perivascular infiltrate composed of mononuclear cells and multinucleated giant cells was observed in the upper and mid dermis&#46; The cytoplasm of these cells contained numerous fragmented elastic fibers rendered more visible by Verhoeff-Van Gieson staining&#46; Neither collagen degeneration nor the presence of mucin were observed &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46;</p><elsevierMultimedia ident="fig0010"></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">Annular elastolytic giant cell granuloma &#40;actinic granuloma&#41;&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Clinical Course and Treatment</span><p id="par0035" class="elsevierStylePara elsevierViewall">Treatment was started with medium-strength topical corticosteroids and sun protection&#46; Partial improvement of the lesions was observed after 3 months of application&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Comment</span><p id="par0040" class="elsevierStylePara elsevierViewall">Annular elastolytic giant cell granuloma &#40;AEGCG&#41;&#44; also known as actinic granuloma or O&#8217;Brien granuloma&#44; is a rare granulomatous disease characterized by the presence of multinucleated giant cells with phagocytosis of anomalous elastic fibers&#44; a process known as elastophagocytosis&#46; AEGCG mainly affects women aged 50 to 70 years with a light skin phototype and signs of chronic actinic damage&#46; The lesions usually begin as erythematous papules that later evolve into annular plaques with raised borders and a minimal atrophic center&#46; The most common sites are sun-exposed areas such as the face&#44; upper chest&#44; and legs&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">1</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">The pathogenesis of this entity is unknown&#44; although the possibility of an autoimmune reaction directed against elastic fibers&#44; determining a granulomatous inflammatory response with the formation of granulomas&#44; has been postulated&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">2</span></a> AEGCG has been described in association with various processes&#44; including diabetes mellitus&#44; medication use&#44; hypothyroidism&#44; thyroiditis&#44; lymphomas&#44; polymyalgia rheumatica&#44; and temporal arteritis&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">At present&#44; it is not known whether there is a relationship between AEGCG and these processes&#46;</p><p id="par0055" class="elsevierStylePara elsevierViewall">Histopathology shows 3 well-defined zones that reflect this possible pathogenesis&#46; A peripheral zone&#44; outside the borders of the plaques&#44; is characterized by a papillary dermis with actinic elastosis&#44; without the presence of multinucleated giant cells or granulomas&#46; This zone&#44; in which the lesion progresses&#44; contains antigenic elastic fibers that have not yet induced an inflammatory reaction&#46; In an intermediate or active zone&#8212;corresponding clinically to the edge of the lesions&#8212;fragmented elastic fibers&#44; elastophagocytosis phenomena&#44; and granuloma formation are observed&#46; Finally&#44; a central zone&#44; characterized by the absence of elastic fibers and few inflammatory cells&#44; is the residual postinflammatory zone&#46;<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">3</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">The main differential diagnosis is granuloma annulare &#40;GA&#41; at sun-exposed sites&#46; In fact&#44; since AEGCG was first described&#44; there has been some debate about whether it is a distinct entity or a variant of GA with elastophagocytosis&#46;<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">4</span></a> Although these two processes can be clinically identical&#44; histologic studies support the idea that they are separate entities&#46; In AEGCG&#44; the granulomatous reaction is found mainly in the upper dermis and no mucin is observed&#44; whereas in GA&#44; granulomas are distributed throughout the upper and mid dermis&#44; forming a palisade around an area characterized by degenerated collagen and the presence of mucin&#46;<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">5</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">Although spontaneous remission has been reported in some cases&#44; AEGCG tends to be chronic and recurring&#46; Multiple treatment options have been described&#44; including sun protection&#59; topical&#44; systemic&#44; or intralesional corticosteroids&#59; chloroquine&#59; dapsone&#59; methotrexate&#59; anti&#8211;tumor necrosis factor &#40;TNF&#41; monoclonal antibodies&#59; and low-dose oral retinoids&#46; These treatments have produced variable results&#46;<a class="elsevierStyleCrossRefs" href="#bib0070"><span class="elsevierStyleSup">6&#8211;8</span></a></p></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflicts of Interest</span><p id="par0070" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest&#46;</p></span></span>"
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2024 Septiembre 67 26 93
2024 Agosto 106 51 157
2024 Julio 90 44 134
2024 Junio 80 33 113
2024 Mayo 63 27 90
2024 Abril 87 34 121
2024 Marzo 75 25 100
2024 Febrero 64 33 97
2024 Enero 54 30 84
2023 Diciembre 66 27 93
2023 Noviembre 98 21 119
2023 Octubre 61 20 81
2023 Septiembre 71 34 105
2023 Agosto 55 12 67
2023 Julio 40 33 73
2023 Junio 50 27 77
2023 Mayo 69 20 89
2023 Abril 58 19 77
2023 Marzo 68 28 96
2023 Febrero 70 32 102
2023 Enero 38 30 68
2022 Diciembre 72 36 108
2022 Noviembre 25 33 58
2022 Octubre 32 21 53
2022 Septiembre 26 40 66
2022 Agosto 30 30 60
2022 Julio 63 34 97
2022 Junio 31 26 57
2022 Mayo 40 47 87
2022 Abril 60 44 104
2022 Marzo 55 60 115
2022 Febrero 35 40 75
2022 Enero 41 57 98
2021 Diciembre 37 52 89
2021 Noviembre 65 55 120
2021 Octubre 52 68 120
2021 Septiembre 38 45 83
2021 Agosto 51 48 99
2021 Julio 42 38 80
2021 Junio 39 44 83
2021 Mayo 41 68 109
2021 Abril 85 137 222
2021 Marzo 65 49 114
2021 Febrero 86 50 136
2021 Enero 48 50 98
2020 Diciembre 38 41 79
2020 Noviembre 40 55 95
2020 Octubre 16 20 36
2020 Septiembre 23 16 39
2020 Agosto 38 30 68
2020 Julio 26 20 46
2020 Junio 34 37 71
2020 Mayo 18 14 32
2020 Abril 19 14 33
2020 Marzo 15 10 25
2020 Febrero 3 1 4
2020 Enero 2 0 2
2019 Diciembre 8 0 8
2019 Noviembre 4 0 4
2019 Septiembre 10 0 10
2019 Agosto 4 0 4
2019 Julio 4 0 4
2019 Junio 4 0 4
2019 Mayo 6 0 6
2019 Abril 2 0 2
2019 Marzo 2 0 2
2019 Febrero 2 0 2
2018 Diciembre 2 0 2
2018 Noviembre 1 0 1
2018 Septiembre 3 0 3
2018 Abril 1 0 1
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