Diffuse cutaneous systemic sclerosis: A case report
Philippine Journal of Internal Medicine
; : 1-4, 2017.
Article
de En
| WPRIM
| ID: wpr-960121
Bibliothèque responsable:
WPRO
ABSTRACT
@#<p style="text-align: justify;"><strong>BACKGROUND: </strong>Systemic sclerosis (SSc) is a rare, connective tissue disease with multisystem involvement.This is due to immunological processes,vascular endothelial cell injury and extensive activation of fibrolast that commonly affects the skin and other internal organs such as the esophagus, lungs, heart, and kidneys. SSc has one of the highest mortality among the autoimmune rheumatic diseases, hence the emphasis on the early recognition and management to prevent significant progression of the disease. <br /><strong>CASE:</strong> A 22-year-old female presented with a one-year history of multiple hard and hypopigmented patches on the face, neck, trunk and upper extremities. Further examination revealed mask-like facies, microstomia, frenulum sclerosis, Raynaud's phenomenon, pitted scars on the digital pulp of hands and sclerodactyly.Baseline blood chemistry,chest radiograph and electrocardiography were all negative for systemic involvement. Autoantibodies were positive for dsDNA, SS-A/Ro and Scl-70. Skin biopsy revealed sclerosing dermatitis, which was consistent with SSc. <br /><strong>OUTCOME:</strong> The patient was initially started with oral prednisone 0.5 mg/kg/day and was increased to 0.75 mg/kg/day for eight weeks. Prednisone was slowly tapered to 5.0 mg/day and methotrexate 15.0 mg/week was included in the management for eight weeks which resulted in decreased joint pains, halted the progression of skin induration, decreased in pruritus and palmar edema. <br /><strong>CONCLUSION:</strong> The characteristic dermatological findings of SSc are not only important signs to dermatologists, but these serves as diagnostic clues for clinicians from other disciplines as well. In our case, the presence of the autoantibody Scl-70 indicated the potential risk of pulmonary fibrosis and pulmonary arterial hypertension that accounts with high mortality.Hence,physicians should be aware of the possible risk of organ damage,even when asymptomatic because there is a high risk of disease progression. The importance of early recognition and a multidisciplinary approach lead to the good outcome in this case.</p>
Mots clés
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Indice:
WPRIM
Sujet Principal:
Fibrose pulmonaire
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Maladie de Raynaud
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Sclérodermie systémique
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Sclérose
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Autoanticorps
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Prednisone
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Méthotrexate
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Rhumatismes
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Cicatrice
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Sclérodermie diffuse
Limites du sujet:
Adult
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Female
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Humans
langue:
En
Texte intégral:
Philippine Journal of Internal Medicine
Année:
2017
Type:
Article