|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
* From the Rush-Presbyterian-St. Luke's Medical Center, Chicago, IL.
Correspondence to: Steven Kesten, MD, FCCP, Rush-Presbyterian-St. Luke's Medical Center, 1725 W. Harrison St, Suite 836, Chicago, IL 60612; e-mail: skesten{at}rush.edu
A young woman with primary pulmonary hypertension presented with interstitial lung disease approximately 5 years after successful treatment with IV prostacyclin. The pathology was consistent with nonspecific interstitial pneumonitis and was unresponsive to steroids and immunosuppressive medications. We speculate that further cases of this syndrome may be reported as more patients are living beyond 5 years with prostacyclin.
Key Words: interstitial lung disease primary pulmonary hypertension prostacyclin
This article has been cited by other articles:
![]() |
H. Morimatsu, K. Goto, T. Matsusaki, H. Katayama, H. Matsubara, T. Ohe, and K. Morita Rapid Development of Severe Interstitial Pneumonia Caused by Epoprostenol in a Patient with Primary Pulmonary Hypertension Anesth. Analg., October 1, 2004; 99(4): 1205 - 1207. [Abstract] [Full Text] [PDF] |
||||
![]() |
A. Resten, S. Maitre, M. Humbert, A. Rabiller, O. Sitbon, F. Capron, G. Simonneau, and D. Musset Pulmonary Hypertension: CT of the Chest in Pulmonary Venoocclusive Disease Am. J. Roentgenol., July 1, 2004; 183(1): 65 - 70. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Archer and S. Rich Primary Pulmonary Hypertension : A Vascular Biology and Translational Research "Work in Progress" Circulation, November 28, 2000; 102(22): 2781 - 2791. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |