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Angioimmunoblastic lymphadenopathy, sulphasalazine exposure and villous atrophy.

A woman with inflammatory lesions in the terminal ileum was treated with sulphasalazine. Nine months later she developed angioimmunoblastic lymphadenopathy and was found to have intestinal villous atrophy. Her systemic illness partially responded to oral steroids but a gluten free diet restored clin...

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Autors principals: Smith, M. A., Steele, P. R., Youngs, G. R.
Format: Artigo
Idioma:Inglês
Publicat: BMJ Group 1985
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2418216/
https://ncbi.nlm.nih.gov/pubmed/2862622
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