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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Acquired Reactive Perforating Dermatosis &#40;ARPD&#41; is a rare group of skin disorders&#44; characterized by transepidermal elimination of various materials&#44; such as collagen&#44; elastin&#44; and keratin&#46; When the elimination occurs through a follicular unit&#44; it is called perforating folliculitis&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The most common systemic diseases associated with ARPD are diabetes mellitus and renal failure&#44; but associations with infectious&#44; inflammatory and autoimmune diseases have been reported&#44; with possible triggers including immunological vasculopathy in the setting of the underlying autoimmune disorder and dermal microangiopathy due to scratching&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 54-year-old woman that was referred to the Dermatology outpatient clinic with a pruritic dermatosis of unknown evolution time&#46; The dermatosis was diffusely distributed bilaterally on her thighs and elbows and was composed of erythematous-violaceus umbilicated papules with central adherent hyperkeratotic plugs &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Koebner phenomenon was present in some of the lesions&#46; The patient had Rheumatoid Arthritis &#40;RA&#41;&#44; positive for both rheumatoid factor and anti-citrullinated protein antibodies&#44; with unsatisfactory control under 12&#46;5&#8239;mg of prednisolone daily&#46; She had never been treated with biological drugs and had recently suspended sulfasalazine due to hepatotoxicity&#46; Blood work revealed a mildly elevated erythrocyte sedimentation rate of 42&#8239;mm&#47;h &#40;normal &#60;29&#8239;mm&#47;h&#41;&#44; but glycemia and kidney function were normal&#46; Considering the cutaneous manifestations associated with rheumatoid arthritis&#44; such as rheumatoid neutrophilic dermatosis and interstitial granulomatosis dermatitis&#44; a punch biopsy was carried out&#46; Histopathology revealed a dilated hair follicle with infundibular disruption&#44; containing keratinous debris and neutrophils&#46; Verhoeff stain evidenced that the eliminated materials were both elastic fibers and collagen &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Consequently&#44; a diagnosis of perforating folliculitis was made&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">After a suboptimal response to topical clobetasol propionate and antihistamines and given the impossibility of safely undergoing phototherapy &#40;the patient had a hearing and cognitive impairment&#41;&#44; initiation of allopurinol 100&#8239;mg&#47;day resulted in a considerable symptomatic relief and almost complete resolution of the dermatosis&#44; with no adverse effects&#46; The patient maintains regular follow at Dermatology and Rheumatology outpatient clinics and has since started abatacept&#44; a disease-modifying anti-rheumatic agent&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">As of today&#44; there are no specific evidence-based guidelines regarding the treatment of perforating dermatosis&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> When possible&#44; the priority should be the control of the underlying disease&#46; Other treatment options include topical or systemic retinoids&#44; antibiotics&#44; topical&#44; intralesional&#44; or systemic glucocorticoids&#44; antihistamines&#44; surgery&#44; narrow-band ultraviolet B phototherapy&#44; PUVA and allopurinol&#46; Allopurinol may be a valid and helpful treatment for ARPD&#44; with successful results reported in 14 case reports and case series&#44; with no reported adverse reactions&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#8211;4</span></a> Its exact mechanism of action is unknown&#44; but it may act via its antioxidant effect due to the inhibition of xanthine oxidase&#46; A recent systematic review suggests it as a first-line systemic treatment&#44; along with antihistamines&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In conclusion&#44; due to the rarity of these diseases and the lack of guidelines&#44; the management of ARPD can be challenging&#46; We present a rare association of perforating folliculitis and rheumatoid arthritis&#44; successfully treated with allopurinol 100&#8239;mg once per day&#46; Our experience supports allopurinol as a safe and effective treatment for ARPD&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0030" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contributions</span><p id="par0035" class="elsevierStylePara elsevierViewall">Ana Gusm&#227;o Palmeiro&#58; Critical literature review&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#59; data collection&#44; analysis and interpretation&#59; preparation and writing of the manuscript&#59; study conception and planning&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Maria Jo&#227;o Gon&#231;alves&#58; Manuscript critical review&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Cristina Amaro&#58; Manuscript critical review&#59; approval of the final version of the manuscript&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#59; study conception and planning&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Isabel Viana&#58; Approval of the final version of the manuscript&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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Letter - Therapy
Acquired reactive perforating dermatosis successfully treated with allopurinol
Ana Gusmão Palmeiroa,
Autor para correspondência
apgpalmeiro@gmail.com

Corresponding author.
, Maria João Gonçalvesb, Cristina Amaroa, Isabel Vianaa
a Dermatology Department, Hospital de Egas Moniz, Centro de Lisboa Ocidental, Lisbon, Portugal
b Rheumatology Department, Hospital de Egas Moniz, Centro de Lisboa Ocidental, Lisbon, Portugal
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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#41; Erythematous papules on the anterior surface of thighs and knees&#59; &#40;B&#41; detail of central adherent hyperkeratotic plugs</p>"
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Acquired Reactive Perforating Dermatosis &#40;ARPD&#41; is a rare group of skin disorders&#44; characterized by transepidermal elimination of various materials&#44; such as collagen&#44; elastin&#44; and keratin&#46; When the elimination occurs through a follicular unit&#44; it is called perforating folliculitis&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The most common systemic diseases associated with ARPD are diabetes mellitus and renal failure&#44; but associations with infectious&#44; inflammatory and autoimmune diseases have been reported&#44; with possible triggers including immunological vasculopathy in the setting of the underlying autoimmune disorder and dermal microangiopathy due to scratching&#46;</p><p id="par0010" class="elsevierStylePara elsevierViewall">We present the case of a 54-year-old woman that was referred to the Dermatology outpatient clinic with a pruritic dermatosis of unknown evolution time&#46; The dermatosis was diffusely distributed bilaterally on her thighs and elbows and was composed of erythematous-violaceus umbilicated papules with central adherent hyperkeratotic plugs &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#41;&#46; Koebner phenomenon was present in some of the lesions&#46; The patient had Rheumatoid Arthritis &#40;RA&#41;&#44; positive for both rheumatoid factor and anti-citrullinated protein antibodies&#44; with unsatisfactory control under 12&#46;5&#8239;mg of prednisolone daily&#46; She had never been treated with biological drugs and had recently suspended sulfasalazine due to hepatotoxicity&#46; Blood work revealed a mildly elevated erythrocyte sedimentation rate of 42&#8239;mm&#47;h &#40;normal &#60;29&#8239;mm&#47;h&#41;&#44; but glycemia and kidney function were normal&#46; Considering the cutaneous manifestations associated with rheumatoid arthritis&#44; such as rheumatoid neutrophilic dermatosis and interstitial granulomatosis dermatitis&#44; a punch biopsy was carried out&#46; Histopathology revealed a dilated hair follicle with infundibular disruption&#44; containing keratinous debris and neutrophils&#46; Verhoeff stain evidenced that the eliminated materials were both elastic fibers and collagen &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Consequently&#44; a diagnosis of perforating folliculitis was made&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">After a suboptimal response to topical clobetasol propionate and antihistamines and given the impossibility of safely undergoing phototherapy &#40;the patient had a hearing and cognitive impairment&#41;&#44; initiation of allopurinol 100&#8239;mg&#47;day resulted in a considerable symptomatic relief and almost complete resolution of the dermatosis&#44; with no adverse effects&#46; The patient maintains regular follow at Dermatology and Rheumatology outpatient clinics and has since started abatacept&#44; a disease-modifying anti-rheumatic agent&#46;</p><p id="par0020" class="elsevierStylePara elsevierViewall">As of today&#44; there are no specific evidence-based guidelines regarding the treatment of perforating dermatosis&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> When possible&#44; the priority should be the control of the underlying disease&#46; Other treatment options include topical or systemic retinoids&#44; antibiotics&#44; topical&#44; intralesional&#44; or systemic glucocorticoids&#44; antihistamines&#44; surgery&#44; narrow-band ultraviolet B phototherapy&#44; PUVA and allopurinol&#46; Allopurinol may be a valid and helpful treatment for ARPD&#44; with successful results reported in 14 case reports and case series&#44; with no reported adverse reactions&#46;<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2&#8211;4</span></a> Its exact mechanism of action is unknown&#44; but it may act via its antioxidant effect due to the inhibition of xanthine oxidase&#46; A recent systematic review suggests it as a first-line systemic treatment&#44; along with antihistamines&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">In conclusion&#44; due to the rarity of these diseases and the lack of guidelines&#44; the management of ARPD can be challenging&#46; We present a rare association of perforating folliculitis and rheumatoid arthritis&#44; successfully treated with allopurinol 100&#8239;mg once per day&#46; Our experience supports allopurinol as a safe and effective treatment for ARPD&#46;</p><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0005">Financial support</span><p id="par0030" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Authors&#8217; contributions</span><p id="par0035" class="elsevierStylePara elsevierViewall">Ana Gusm&#227;o Palmeiro&#58; Critical literature review&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#59; data collection&#44; analysis and interpretation&#59; preparation and writing of the manuscript&#59; study conception and planning&#46;</p><p id="par0040" class="elsevierStylePara elsevierViewall">Maria Jo&#227;o Gon&#231;alves&#58; Manuscript critical review&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#46;</p><p id="par0045" class="elsevierStylePara elsevierViewall">Cristina Amaro&#58; Manuscript critical review&#59; approval of the final version of the manuscript&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#59; study conception and planning&#46;</p><p id="par0050" class="elsevierStylePara elsevierViewall">Isabel Viana&#58; Approval of the final version of the manuscript&#59; intellectual participation in propaedeutic and&#47;or therapeutic&#59; management of studied cases&#46;</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Conflicts of interest</span><p id="par0055" class="elsevierStylePara elsevierViewall">None declared&#46;</p></span></span>"
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