|
|||
| |||||||||||||||||||||||||||||||||||||||||
Dr. David M. Dudzinski (Medicine): Fever and abdominal pain and distention developed in a 34-year-old man with cystic fibrosis during an admission to this hospital for pulmonary care.
The patient was awaiting lung transplantation for end-stage lung disease due to cystic fibrosis. Cystic fibrosis had been diagnosed at birth, and he was homozygous for the F508 mutation in the cystic fibrosis transmembrane conductance regulator gene (CFTR). He had been hospitalized at least annually for complications of the disease, most recently 1 year earlier because of pneumonia caused by Pseudomonas aeruginosa and methicillin-resistant Staphylococcus aureus. His daily pulmonary
Differential Diagnosis
Vascular Events
Obstruction
Inflammation
Infection
Management of C. difficile Colitis
Summary
Clinical Diagnosis
Dr. Steven D. Freedman's Diagnosis
Pathological Discussion
Anatomical Diagnoses
Source Information
From the Department of Medicine, Beth Israel Deaconess Medical Center (S.D.F.); the Departments of Radiology (R.N.U.) and Pathology (M.M.-K.), Massachusetts General Hospital; and the Departments of Medicine (S.D.F.), Radiology (R.N.U.), and Pathology (M.M.-K.), Harvard Medical School — all in Boston.
HOME | SUBSCRIBE | SEARCH | CURRENT ISSUE | PAST ISSUES | COLLECTIONS | PRIVACY | TERMS OF USE | HELP | beta.nejm.org Comments and questions? Please contact us. The New England Journal of Medicine is owned, published, and copyrighted © 2009 Massachusetts Medical Society. All rights reserved. |