Abstract
We report the coincidence of hereditary angioedema and rheumatoid arthritis in a male patient and in his father. During treatment with D-penicillamine the patient developed a transient lupus-like disorder with glomerulonephritis that resolved when D-penicillamine was discontinued. He later was diagnosed with malignant lymphoma. Impaired classical complement pathway function could have contributed to development of the drug reaction.
Publication types
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Case Reports
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Research Support, Non-U.S. Gov't
MeSH terms
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Angioedema / complications
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Angioedema / genetics
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Arthritis, Rheumatoid / blood*
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Arthritis, Rheumatoid / complications
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Arthritis, Rheumatoid / drug therapy*
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Child
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Complement C1 Inactivator Proteins / deficiency*
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Glomerulonephritis / chemically induced
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Glomerulonephritis / pathology
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Humans
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Lupus Erythematosus, Systemic / chemically induced
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Male
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Penicillamine / adverse effects*
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Penicillamine / therapeutic use
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Risk Factors
Substances
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Complement C1 Inactivator Proteins
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Penicillamine