A Case of Progressive Systemic Scleroderma Associated with Malignant Fibrous Histiocytoma.
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A case of progressive systemic scleroderma associated with malignant fibrous histiocytoma is reported. A 58-year-old male first noticed Raynaud phenomenon five years ago. Gradually, pigmentation spread across the whole body, sclerodactyly and lung fibrosis appeared. He was diagnosed as progressive systemic scleroderma in 1991 and was treated with d-penicilamin and oral corticosteroid. In July 1992, sudden onset of chest pain occurred. Chest X-ray revealed pleural exudate in the left lower lobe. Sternal puncture was performed but pain increased and the patient developed respiratory insufficiency, resulting in death. Pleural biopsy had suggested mesothelioma of the pleura, but postmortem findings indicated malignant fibrous histiocytoma.
- 日本皮膚科学会大阪地方会の論文
日本皮膚科学会大阪地方会 | 論文
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