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1.
Korean Journal of Medicine ; : 593-596, 2001.
Article Dans Coréen | WPRIM | ID: wpr-158608

Résumé

Thrombotic thrombocytopenic purpura (TTP) rarely may be seen in association with autoimmune processes such as scleroderma, rheumatoid arthritis, polyarteritis nodosa, Sj gren's syndrome, and systemic lupus erythematosusus (SLE). The diagnosis of TTP as a syndrome distinct from SLE may be challenging, because both processes may present with some or all elements of the classic pentad considered pathognomonic of the former: microangiopathic hemolytic anemia, fever, thrombocytopenia, neurological deficits, and renal abnormalities. We describe a patient with synchronous TTP and SLE, and review the literature.


Sujets)
Humains , Anémie hémolytique , Polyarthrite rhumatoïde , Diagnostic , Fièvre , Lupus érythémateux disséminé , Polyartérite noueuse , Purpura thrombotique thrombocytopénique , Thrombopénie
2.
Korean Journal of Medicine ; : 452-456, 2000.
Article Dans Coréen | WPRIM | ID: wpr-151052

Résumé

Malignant fibrous histiocytoma(MFH) is a high grade soft tissue sarcoma, commonly occur in the retroperitoneum, extremities, head and neck in the patient with old ages. But it is very uncommon that MFH primarily occurs in the lung, and uncommon in young ages. We experienced a young male patient with primary MFH of the lung. The patient had huge masses on both lungs which were diagnosed as MFH by thoracoscopy-guided wedge resection of mass, so we could not perform operative management. And we tried 6 cycles of chemotherapy using ifosfamide, doxorubicin, dacarbazine. After chemotherapy, masses still remained in spite of decreasing sizes.


Sujets)
Humains , Mâle , Dacarbazine , Doxorubicine , Traitement médicamenteux , Membres , Tête , Histiocytome , Histiocytome fibreux malin , Ifosfamide , Poumon , Cou , Sarcomes , Thoracoscopie
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