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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
Corresponding author
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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    "titulo" => "Bilateral Annular Plaques on the Hands and Forearms"
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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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Article information
ISSN: 15782190
Original language: English
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2023 November 98 21 119
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2023 September 71 34 105
2023 August 55 12 67
2023 July 40 33 73
2023 June 50 27 77
2023 May 69 20 89
2023 April 58 19 77
2023 March 68 28 96
2023 February 70 32 102
2023 January 38 30 68
2022 December 72 36 108
2022 November 25 33 58
2022 October 32 21 53
2022 September 26 40 66
2022 August 30 30 60
2022 July 63 34 97
2022 June 31 26 57
2022 May 40 47 87
2022 April 60 44 104
2022 March 55 60 115
2022 February 35 40 75
2022 January 41 57 98
2021 December 37 52 89
2021 November 65 55 120
2021 October 52 68 120
2021 September 38 45 83
2021 August 51 48 99
2021 July 42 38 80
2021 June 39 44 83
2021 May 41 68 109
2021 April 85 137 222
2021 March 65 49 114
2021 February 86 50 136
2021 January 48 50 98
2020 December 38 41 79
2020 November 40 55 95
2020 October 16 20 36
2020 September 23 16 39
2020 August 38 30 68
2020 July 26 20 46
2020 June 34 37 71
2020 May 18 14 32
2020 April 19 14 33
2020 March 15 10 25
2020 February 3 1 4
2020 January 2 0 2
2019 December 8 0 8
2019 November 4 0 4
2019 September 10 0 10
2019 August 4 0 4
2019 July 4 0 4
2019 June 4 0 4
2019 May 6 0 6
2019 April 2 0 2
2019 March 2 0 2
2019 February 2 0 2
2018 December 2 0 2
2018 November 1 0 1
2018 September 3 0 3
2018 April 1 0 1
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Idiomas
Actas Dermo-Sifiliográficas
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¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?