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논문 기본 정보

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학술저널
저자정보
Harold Henrison Chiu (Division of Endocrinology Department of Medicine Philippine General Hospital University of the Phil) Patricia Pauline Remalante (Division of Rheumatology Department of Medicine Philippine General Hospital University of the Phili) Patricia Nacianceno (Department of Dermatology Philippine General Hospital University of the Philippines Manila Manila P) Rogelio Velasco Jr. (Division of Oncology Department of Medicine Philippine General Hospital University of the Philippin) Ramon Larrazabal Jr. (Department of Medicine Philippine General Hospital University of the Philippines Manila Manila Phil) Geraldine Zamora (Division of Rheumatology Department of Medicine Philippine General Hospital University of the Phili)
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대한류마티스학회 대한류마티스학회지 대한류마티스학회지 제27권 제4호
발행연도
2020.1
수록면
285 - 289 (5page)

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Dermatomyositis is a rare disease characterized by classic skin lesions and muscle weakness. In rare cases, life-threatening hypercalcemia may develop caused by regression of dystrophic calcifications. Here we report a 36-year-old man who presented with progressive proximal weakness, difficulty in ambulation, and weight loss. He had the V-sign, Gottron’s papules, and hard, chalky nodules on both antecubital, thigh, and hip areas. Laboratory examinations revealed hypercalcemia (3.47 mmol/L) and shortened QT interval. Workup for malignancy and tuberculosis yielded negative results. Biopsy of the antecubital areas revealed calcinosis cutis. Serum calcium levels gradually normalized with hydration and steroids. Our case illustrated that a high index of suspicion for dermatomyositis is warranted for early diagnosis and ascertaining the etiology of hypercalcemia is vital in the management of this life-threatening complication. While hypercalcemia from dermatomyositis may respond to steroids, to date, individualization of treatment remains the standard of care.

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