Jump to content

Secondary sclerosing cholangitis

From Wikipedia, the free encyclopedia
This is an old revision of this page, as edited by Madhero88 (talk | contribs) at 17:15, 7 March 2009 (Created page with ''''Secondary sclerosing cholangitis''' abbreviated as ('''SSC''') is a disease that is morphologically similar to primary sclerosing cholangitis ([[primary scle…'). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)

Secondary sclerosing cholangitis abbreviated as (SSC) is a disease that is morphologically similar to primary sclerosing cholangitis (PSC) but that originates from a known pathological process. Its clinical and cholangiographic features may mimic PSC, yet its natural history may be more favorable if recognition is prompt and appropriate therapy is introduced. Thus, the diagnosis of PSC requires the exclusion of secondary causes of sclerosing cholangitis and recognition of associated conditions that may potentially imitate its classic cholangiographic features. Secondary causes of SSC include intraductal stone disease, surgical or blunt abdominal trauma, intra-arterial chemotherapy, and recurrent pancreatitis.[1]

Reference

  1. ^ Abdalian R, Heathcote EJ (2006). "Sclerosing cholangitis: a focus on secondary causes". Hepatology. 44 (5): 1063–74. doi:10.1002/hep.21405. PMID 17058222. {{cite journal}}: Unknown parameter |month= ignored (help)