Relapsing polychondritis and myelodysplasia
| Autor: | I Richmond, L Sellars, K Bel'eed, M J Wright |
|---|---|
| Rok vydání: | 1997 |
| Předmět: |
Male
Chondropathy Systemic disease Pathology medicine.medical_specialty Laryngeal Cartilages Eye disease Diuresis Bone Marrow medicine Humans Polychondritis Relapsing Nose Relapsing polychondritis Aged Transplantation business.industry medicine.disease Spine medicine.anatomical_structure Nephrology Myelodysplastic Syndromes Kidney Diseases business Complication Kidney disease |
| Zdroj: | Nephrology Dialysis Transplantation. 12:1704-1707 |
| ISSN: | 1460-2385 0931-0509 |
| DOI: | 10.1093/ndt/12.8.1704 |
| Popis: | Relapsing polychondritis (RP) is characterized by promicroscopy confirmed the presence of red cells, but gressive inflammatory destruction of glycosaminoglycans-containing tissues throughout the body. It there were no casts or urate crystals. Abdominal ultratypically presents in late middle-age with recurrent sound was normal. It was felt that the most likely painful swelling of the external ear or nose and is often cause of the worsening renal function was diclofenac associated with an asymmetrical, non-erosive seroneg- exposure so this was withdrawn. A diuresis was success |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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