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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Subcutaneous sarcoidosis accounts for between 1&#46;4&#37; and 6&#37; of skin lesions attributable to sarcoidosis&#44; making it the least common subtype of specific lesion of this disease&#46; It mainly affects white women in the fifth and sixth decades of life&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The lesions are typically firm&#44; round or fusiform nodules with a diameter of between 0&#46;5 and 2<span class="elsevierStyleHsp" style=""></span>cm&#59; they are mainly found in varying numbers on the upper limbs and are usually bilateral and asymmetric&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Diagnosis requires histologic evidence of noncaseating granulomas in the subcutaneous tissue&#44; without microorganisms&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">We report the case of a 78-year-old woman with intrinsic asthma diagnosed 3 years earlier who developed subcutaneous sarcoidosis with marked fibroplasia&#46; The patient had consulted for a mass that had appeared on her left forearm a year earlier&#44; a similar mass on her right forearm&#44; which had appeared a month later&#44; and a third mass&#44; which had appeared on her right elbow 3 months before consultation&#46; Both she and her family commented that the size of the lesions had remained stable and that they were slightly tender&#46; The only systemic symptom she reported was occasional joint pain in her upper limbs&#46; Physical examination revealed 2 hard nodules&#44; one on the left forearm and one in the right cubital region&#44; measuring 2&#46;5&#160;and 5<span class="elsevierStyleHsp" style=""></span>cm respectively&#46; They were not fixed to the deeper layers and there were no visible epidermal changes&#46; A third&#44; similar lesion&#44; with a stony-hard consistency and also not adherent to the deeper layers&#44; was observed on the right forearm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#44; A and B&#41;&#46; Biopsy of the nodule on the right elbow showed a central area of sclerotic tissue with numerous sarcoid granulomas visible in the subcutaneous tissue &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46; Also visible was a discrete lymphocytic infiltrate&#46; There were no foci of necrosis&#46; An ultrasound scan of the right forearm showed a well-circumscribed&#44; nonencapsulated&#44; oval mass measuring 4&#46;3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>1&#46;2<span class="elsevierStyleHsp" style=""></span>cm&#44; with no muscle or bone involvement&#59; the mass was slightly hyperechogenic and contained hypoechoic areas that gave it a mottled appearance&#46; The chest scan showed hilar enlargement&#44; which was confirmed on high-resolution computed tomography&#44; which also revealed a reticulonodular infiltrate in both lungs&#46; Spirometry showed an obstructive pattern&#44; with a forced expiratory volume in the first second to forced vital capacity ratio of 66&#37; of predicted&#46; The electrocardiogram was normal and the Mantoux test was negative&#46; Laboratory tests revealed an elevated creatinine level &#40;2&#46;08<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; an increased calcium to creatinine clearance ratio &#40;0&#46;64&#59; normal range&#44; 0&#46;07-0&#46;17<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; and decreased tubular reabsorption of phosphate &#40;51&#37;&#59; normal range&#44; 79&#37;-89&#37;&#41;&#46; Serum levels of vitamin D&#44; parathyroid hormone&#44; calcium&#44; phosphorous&#44; and angiotensin-converting enzyme were within normal limits&#46; No eye alterations were detected&#46; Once the diagnosis of sarcoidosis was confirmed by clinical&#44; histologic&#44; and radiologic findings&#44; the patient was started on prednisone&#44; 30<span class="elsevierStyleHsp" style=""></span>mg once daily&#44; for 6 weeks&#59; the treatment resulted in a considerable improvement in the respiratory symptoms and a reduction in the size of the nodules&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Clinically&#44; the nodules of subcutaneous sarcoidosis are rather nonspecific&#44; although P&#233;rez-Cejudo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> remarked that they could adopt an elongated form&#44; but without forming cords as occurs in interstitial granulomatous dermatitis with arthritis&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Nevertheless&#44; because of the nodular nature of the lesions&#44; the differential diagnosis must include conditions associated with substance deposition&#44; cysts&#44; lipomas&#44; calcinosis&#44; rheumatoid nodules&#44; metastases&#44; tuberculosis&#44; cellulitis&#44; and even breast cancer&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">While few studies have analyzed the histologic features of subcutaneous sarcoidosis&#44; it has been suggested that it is a predominantly lobular panniculitis&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> It is therefore important to differentiate it from other forms of granulomatous lobular panniculitis such as Q fever&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Additionally&#44; because of its granulomatous nature&#44; subcutaneous sarcoidosis needs to be differentiated from certain forms of granulomatous septal panniculitis &#40;which are occasionally induced by drugs<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> or trauma&#41;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> as well as from erythema nodosum&#46; Although this last entity is classified as a predominantly septal panniculitis&#44; when it involves epithelioid granulomas&#44; histology findings can resemble those seen in what has been described by some authors as granulomatous and fibrosing predominantly lobular panniculitis&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> Fibroplasia in subcutaneous sarcoidosis&#44; while not mentioned in most text books&#44; is a characteristic finding and should be expected as it tends to occur extensively in pulmonary sarcoidosis&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> There are several factors that distinguish subcutaneous sarcoidosis from erythema nodosum with epithelioid granulomas&#44; the main differential diagnosis&#58; it is predominantly lobular rather than septal&#44; it has a larger granulomatous than fibroplastic component&#44; the fibroplasia tends to be limited to the perigranulomatous area&#44; there is no evidence of Miescher&#39;s radial granulomas&#44; and eosinophils and neutrophils are rarely seen in the inflammatory infiltrate&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">It is not yet known whether the extent of fibroplasia is related to the duration of the lesions or to the intensity of the lymphocytic infiltrate&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> but a histologic finding of fibrosing granulomatous panniculitis may be considered to be highly specific for subcutaneous sarcoidosis&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p></span>"
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Case and Research Letters
Fibrosing Cutaneous Sarcoidosis
Paniculitis sarcoidea fibrosante
M. Llamas-Velasco
Autor para correspondencia
mar.llamasvelasco@gmail.com

Corresponding author.
, A. Godoy, J. Fraga, J. Sánchez-Pérez
Servicio de Dermatología, Hospital Universitario de La Princesa, Madrid, Spain
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    "textoCompleto" => "<span class="elsevierStyleSections"><p id="par0005" class="elsevierStylePara elsevierViewall">Subcutaneous sarcoidosis accounts for between 1&#46;4&#37; and 6&#37; of skin lesions attributable to sarcoidosis&#44; making it the least common subtype of specific lesion of this disease&#46; It mainly affects white women in the fifth and sixth decades of life&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> The lesions are typically firm&#44; round or fusiform nodules with a diameter of between 0&#46;5 and 2<span class="elsevierStyleHsp" style=""></span>cm&#59; they are mainly found in varying numbers on the upper limbs and are usually bilateral and asymmetric&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> Diagnosis requires histologic evidence of noncaseating granulomas in the subcutaneous tissue&#44; without microorganisms&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">We report the case of a 78-year-old woman with intrinsic asthma diagnosed 3 years earlier who developed subcutaneous sarcoidosis with marked fibroplasia&#46; The patient had consulted for a mass that had appeared on her left forearm a year earlier&#44; a similar mass on her right forearm&#44; which had appeared a month later&#44; and a third mass&#44; which had appeared on her right elbow 3 months before consultation&#46; Both she and her family commented that the size of the lesions had remained stable and that they were slightly tender&#46; The only systemic symptom she reported was occasional joint pain in her upper limbs&#46; Physical examination revealed 2 hard nodules&#44; one on the left forearm and one in the right cubital region&#44; measuring 2&#46;5&#160;and 5<span class="elsevierStyleHsp" style=""></span>cm respectively&#46; They were not fixed to the deeper layers and there were no visible epidermal changes&#46; A third&#44; similar lesion&#44; with a stony-hard consistency and also not adherent to the deeper layers&#44; was observed on the right forearm &#40;<a class="elsevierStyleCrossRef" href="#fig0005">Fig&#46; 1</a>&#44; A and B&#41;&#46; Biopsy of the nodule on the right elbow showed a central area of sclerotic tissue with numerous sarcoid granulomas visible in the subcutaneous tissue &#40;<a class="elsevierStyleCrossRefs" href="#fig0010">Figs&#46; 2 and 3</a>&#41;&#46; Also visible was a discrete lymphocytic infiltrate&#46; There were no foci of necrosis&#46; An ultrasound scan of the right forearm showed a well-circumscribed&#44; nonencapsulated&#44; oval mass measuring 4&#46;3<span class="elsevierStyleHsp" style=""></span>&#215;<span class="elsevierStyleHsp" style=""></span>1&#46;2<span class="elsevierStyleHsp" style=""></span>cm&#44; with no muscle or bone involvement&#59; the mass was slightly hyperechogenic and contained hypoechoic areas that gave it a mottled appearance&#46; The chest scan showed hilar enlargement&#44; which was confirmed on high-resolution computed tomography&#44; which also revealed a reticulonodular infiltrate in both lungs&#46; Spirometry showed an obstructive pattern&#44; with a forced expiratory volume in the first second to forced vital capacity ratio of 66&#37; of predicted&#46; The electrocardiogram was normal and the Mantoux test was negative&#46; Laboratory tests revealed an elevated creatinine level &#40;2&#46;08<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; an increased calcium to creatinine clearance ratio &#40;0&#46;64&#59; normal range&#44; 0&#46;07-0&#46;17<span class="elsevierStyleHsp" style=""></span>mg&#47;dL&#41;&#44; and decreased tubular reabsorption of phosphate &#40;51&#37;&#59; normal range&#44; 79&#37;-89&#37;&#41;&#46; Serum levels of vitamin D&#44; parathyroid hormone&#44; calcium&#44; phosphorous&#44; and angiotensin-converting enzyme were within normal limits&#46; No eye alterations were detected&#46; Once the diagnosis of sarcoidosis was confirmed by clinical&#44; histologic&#44; and radiologic findings&#44; the patient was started on prednisone&#44; 30<span class="elsevierStyleHsp" style=""></span>mg once daily&#44; for 6 weeks&#59; the treatment resulted in a considerable improvement in the respiratory symptoms and a reduction in the size of the nodules&#46;</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia><elsevierMultimedia ident="fig0010"></elsevierMultimedia><elsevierMultimedia ident="fig0015"></elsevierMultimedia><p id="par0015" class="elsevierStylePara elsevierViewall">Clinically&#44; the nodules of subcutaneous sarcoidosis are rather nonspecific&#44; although P&#233;rez-Cejudo et al&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> remarked that they could adopt an elongated form&#44; but without forming cords as occurs in interstitial granulomatous dermatitis with arthritis&#46;<a class="elsevierStyleCrossRef" href="#bib0010"><span class="elsevierStyleSup">2</span></a> Nevertheless&#44; because of the nodular nature of the lesions&#44; the differential diagnosis must include conditions associated with substance deposition&#44; cysts&#44; lipomas&#44; calcinosis&#44; rheumatoid nodules&#44; metastases&#44; tuberculosis&#44; cellulitis&#44; and even breast cancer&#46;<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a></p><p id="par0020" class="elsevierStylePara elsevierViewall">While few studies have analyzed the histologic features of subcutaneous sarcoidosis&#44; it has been suggested that it is a predominantly lobular panniculitis&#46;<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3&#44;4</span></a> It is therefore important to differentiate it from other forms of granulomatous lobular panniculitis such as Q fever&#46;<a class="elsevierStyleCrossRef" href="#bib0025"><span class="elsevierStyleSup">5</span></a> Additionally&#44; because of its granulomatous nature&#44; subcutaneous sarcoidosis needs to be differentiated from certain forms of granulomatous septal panniculitis &#40;which are occasionally induced by drugs<a class="elsevierStyleCrossRefs" href="#bib0030"><span class="elsevierStyleSup">6&#44;7</span></a> or trauma&#41;<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> as well as from erythema nodosum&#46; Although this last entity is classified as a predominantly septal panniculitis&#44; when it involves epithelioid granulomas&#44; histology findings can resemble those seen in what has been described by some authors as granulomatous and fibrosing predominantly lobular panniculitis&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> Fibroplasia in subcutaneous sarcoidosis&#44; while not mentioned in most text books&#44; is a characteristic finding and should be expected as it tends to occur extensively in pulmonary sarcoidosis&#46;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> There are several factors that distinguish subcutaneous sarcoidosis from erythema nodosum with epithelioid granulomas&#44; the main differential diagnosis&#58; it is predominantly lobular rather than septal&#44; it has a larger granulomatous than fibroplastic component&#44; the fibroplasia tends to be limited to the perigranulomatous area&#44; there is no evidence of Miescher&#39;s radial granulomas&#44; and eosinophils and neutrophils are rarely seen in the inflammatory infiltrate&#46;</p><p id="par0025" class="elsevierStylePara elsevierViewall">It is not yet known whether the extent of fibroplasia is related to the duration of the lesions or to the intensity of the lymphocytic infiltrate&#44;<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> but a histologic finding of fibrosing granulomatous panniculitis may be considered to be highly specific for subcutaneous sarcoidosis&#46;<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a></p></span>"
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        "nota" => "<p class="elsevierStyleNotepara">Please cite this article as&#58; Llamas-Velasco M&#44; et al&#46; Paniculitis sarcoidea fibrosante&#46; Actas Dermosifiliogr&#46;2012&#59;103&#58;331-3&#46;</p>"
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