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          "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">&#40;A&#44; B&#41; Deformity and swelling on the lateral face of the IPJ of the second&#44; third and fourth fingers&#44; with predominance on the right hand &#40;arrows&#41;&#46;</p>"
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HLA-B27&#44; rheumatoid factor and antinuclear antibodies&#44; was normal or negative&#46; Plain X-ray showed an increase in soft tissue on the second&#44; third and fourth IPJ of the right hand&#44; with no signs of associated joint or bone involvement &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Magnetic resonance imaging showed oedema and increased soft tissue on the second&#44; third and fourth fingers of the right hand&#46; There were no signs of synovitis or associated collections &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; A skin biopsy was performed that revealed compact hyperkeratosis and thickening of the dermis&#44; with an increase in the number of collagen fibres and fibroblasts&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">This led to a diagnosis of classical pachydermodactyly&#59; given the benign nature of this entity and the absence of associated clinical symptoms a wait-and-see approach was decided&#46; After 18 months of six-monthly follow-up in the paediatric dermatology and rheumatology clinic&#44; the patient remains asymptomatic&#44; without pain&#44; functional limitation or other associated clinical manifestations&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Discussion</span><p id="par0020" class="elsevierStylePara elsevierViewall">Paquidermodactyly&#44; initially described in 1973<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> and later in 1975&#44;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> is an acquired and under-diagnosed form of digital fibromatosis&#44; of benign course and predominantly affects young males&#46; It is characterised by the presence of progressive&#44; 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This document is held by the corresponding author&#46;</p></span></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflict of interests</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have no conflict of interest to declare&#46;</p></span></span>"
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Images in Clinical Rheumatology
Pachydermodactyly: The great mimicker
Paquidermodactilia: la gran simuladora
José Luis Agudo-Menaa,
Corresponding author
agudo.mena@gmail.com

Corresponding author.
, María Isabel Buedo-Rubiob, Eva María García-Atienzac, Eduardo Escario-Travesedoa
a Servicio de Dermatología, Complejo Hospitalario Universitario de Albacete, Albacete, Spain
b Servicio de Pediatría, Complejo Hospitalario Universitario de Albacete, Albacete, Spain
c Gerencia de Atención Integrada, Centro de Salud Zona VIII, Albacete, Spain
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HLA-B27&#44; rheumatoid factor and antinuclear antibodies&#44; was normal or negative&#46; Plain X-ray showed an increase in soft tissue on the second&#44; third and fourth IPJ of the right hand&#44; with no signs of associated joint or bone involvement &#40;<a class="elsevierStyleCrossRef" href="#fig0010">Fig&#46; 2</a>&#41;&#46; Magnetic resonance imaging showed oedema and increased soft tissue on the second&#44; third and fourth fingers of the right hand&#46; There were no signs of synovitis or associated collections &#40;<a class="elsevierStyleCrossRef" href="#fig0015">Fig&#46; 3</a>&#41;&#46; A skin biopsy was performed that revealed compact hyperkeratosis and thickening of the dermis&#44; with an increase in the number of collagen fibres and fibroblasts&#46;</p><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">This led to a diagnosis of classical pachydermodactyly&#59; given the benign nature of this entity and the absence of associated clinical symptoms a wait-and-see approach was decided&#46; After 18 months of six-monthly follow-up in the paediatric dermatology and rheumatology clinic&#44; the patient remains asymptomatic&#44; without pain&#44; functional limitation or other associated clinical manifestations&#46;</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0010">Discussion</span><p id="par0020" class="elsevierStylePara elsevierViewall">Paquidermodactyly&#44; initially described in 1973<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">1</span></a> and later in 1975&#44;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">2</span></a> is an acquired and under-diagnosed form of digital fibromatosis&#44; of benign course and predominantly affects young males&#46; It is characterised by the presence of progressive&#44; asymptomatic and bilateral swelling of the IP joints of both hands&#46;<a class="elsevierStyleCrossRefs" href="#bib0035"><span class="elsevierStyleSup">1&#8211;3</span></a> The cause is unknown&#44; although the possible implication of repeated micro trauma&#44; genetic and hormonal factors has been postulated&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#44;5</span></a> Diagnosis of this entity is essentially clinical&#44; and must be differentiated from juvenile idiopathic arthritis&#44; with characteristic clinical&#44; analytical and radiological findings&#46;<a class="elsevierStyleCrossRefs" href="#bib0050"><span class="elsevierStyleSup">4&#8211;6</span></a> Clinical treatment measures are preferred&#44; although intralesional glucocorticoids could be used&#44; and surgery as an alternative in some subgroups of patients&#46;<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">3&#8211;6</span></a></p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0015">Ethical responsibilities</span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0020">Protection of people and animals</span><p id="par0025" class="elsevierStylePara elsevierViewall">The authors declare that neither human nor animal testing has been carried out under this research&#46;</p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Data confidentiality</span><p id="par0030" class="elsevierStylePara elsevierViewall">The authors declare that they have complied with their work centre protocols for the publication of patient data&#46;</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Right to privacy and informed consent</span><p id="par0035" class="elsevierStylePara elsevierViewall">The authors have obtained the informed consent of the patients and&#47;or subjects referred to in the article&#46; This document is held by the corresponding author&#46;</p></span></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Conflict of interests</span><p id="par0040" class="elsevierStylePara elsevierViewall">The authors have no conflict of interest to declare&#46;</p></span></span>"
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Idiomas
Reumatología Clínica (English Edition)
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