Relay-Version: version B 2.10 5/3/83; site utzoo.UUCP Path: utzoo!mnetor!seismo!lll-crg!nike!rutgers!husc6!harvard!spdcc!dyer From: dyer@spdcc.UUCP (Steve Dyer) Newsgroups: sci.med Subject: Re: Sarcoidosis -- info reqestuested Message-ID: <460@spdcc.UUCP> Date: Sun, 9-Nov-86 16:22:23 EST Article-I.D.: spdcc.460 Posted: Sun Nov 9 16:22:23 1986 Date-Received: Sun, 9-Nov-86 21:01:27 EST References: <1217@ihwpt.UUCP> Distribution: net Organization: S.P. Dyer Computer Consulting, Cambridge MA Lines: 26 In article <1217@ihwpt.UUCP>, knudsen@ihwpt.UUCP (mike knudsen) writes: > After months of coughing up phlegm, my mother was diagnosed > as having sarcoidosis, an inflammation of tissues around > the trachea, or thereabouts. > Can anybody give me an explanation for this condition? > What sort of prognosis to expect? Is it hereditary? Sarcoidosis is a granulomatous disease caused by the accumulation of helper T-cells and mononuclear phagocytes at a variety of organ systems, but the lungs are often the focus of measurable clinical impairment. Its etiology is unknown. I don't believe it's hereditary, although its incidence is much higher in certain groups than others: in America, blacks outnumber whites with the disease by a ratio of roughly 10/1. This ratio isn't maintained elsewhere, however, so it's hard to come to any conclusions. Treatment is conservative, depending on the severity of symptoms. The disease usually is self-limiting in about 50% of patients, though it can also be chronic or recurring. The prognosis is generally good, with either uneventful recovery or mild clinical impairment which can be managed. Your mileage may very, however. Corticosteroids are used, if necessary, although if used injudiciously, their side-effects can be much worse than the underlying disease. -- Steve Dyer dyer@harvard.HARVARD.EDU {linus,wanginst,bbnccv,harvard,ima,ihnp4}!spdcc!dyer