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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">An 8-year-old girl visited our department with painful joints&#44; discomfort in the buccal&#44; eye and genital mucosa&#44; associated with a pruriginous skin rash on the torso and limbs&#44; which had appeared 2 days earlier&#46; A month earlier&#44; she had presented gastroenteritis with a negative stool test&#44; which remitted spontaneously&#59; she had also presented recurring mouth ulcers in the previous 4 months&#46; The patient was assessed by the rheumatology department and was diagnosed with asymmetrical oligoarthritis of the right knee&#44; ankle and elbow&#46; The ophthalmological examination revealed iridocyclitis&#46; The dermatologic examination found vulvar erythema with no ulcers&#44; mouth ulcers&#44; and erythematous and edematous plaques with bullae on the periphery in the form of a string of pearls on the inner surface of both thighs &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>A&#41;&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><p id="par0010" class="elsevierStylePara elsevierViewall">Basic biochemistry&#44; complete blood count&#44; urine analysis&#44; electrophoresis&#44; and immunoglobulin and complement levels were normal&#46; The autoimmune study&#44; which included antinuclear antibodies&#44; anti-Ro&#44; anti-La&#44; and IgA antitransglutaminase antibodies&#44; was negative&#46; The biopsy revealed subepidermal edema and dense neutrophilic infiltration of the dermis with leukocytoclasia without vasculitis &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>B&#41;&#46; Direct immunofluorescence was negative&#46; HLA-B27 haplotype was negative&#46;</p><p id="par0015" class="elsevierStylePara elsevierViewall">Treatment was instated with prednisone 0&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;kg&#47;d and colchicine 0&#46;5<span class="elsevierStyleHsp" style=""></span>mg&#47;d&#44; clinical symptoms improved and the lesions disappeared&#46; The history of recurring mouth ulcers and the clinical and immunologic findings suggested a diagnosis of Beh&#231;et disease&#46; The main differential diagnosis in these lesions should include linear IgA bullous dermatosis&#44; chronic bullous disease of childhood&#44; dermatitis herpetiformis&#44; and reactive arthritis&#46;</p></span>"
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Images in Dermatology
Behçet Disease
Enfermedad de Behçet
A. Imbernón-Moyaa,
Autor para correspondencia
adrian_imber88@hotmail.com

Corresponding author.
, P. Collado-Ramosb, R. Díaz-Delgadoc
a Servicio de Dermatología, Hospital Universitario Severo Ochoa, Leganés, Madrid, Spain
b Servicio de Reumatología, Hospital Universitario Severo Ochoa, Leganés, Madrid, Spain
c Servicio de Pediatría, Hospital Universitario Severo Ochoa, Leganés, Madrid, Spain
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