Abstract：
:Rheumatoid arthritis, in common with other systemic autoimmune diseases, can involve several other organs presenting with complex immunological manifestations. Immune thrombocytopenic purpura caused by an autoimmune reaction against platelets is an infrequent haematological complications. A female patient with rheumatoid arthritis rapidly developed extremely severe immune thrombocytopenic purpura upon suspending oral corticosteroid therapy. Besides the involvement of the mucosa of the coecum, ascending colon and the gastric antrum, the situation was further complicated by bleeding of a gastric polyp, at the nadir of the thrombocytopenic crisis. The bleeding was managed by endoscopic intervention and platelet count recovered upon high dose corticosteroid treatment within a couple of days.
journal_name
Joint Bone Spinejournal_title
Joint bone spineauthors
Gál I,Tóth L,Szegedi L,Kiss GGdoi
10.1016/j.jbspin.2007.06.010subject
Has Abstractpub_date
2008-05-01 00:00:00pages
350-2issue
3eissn
1297-319Xissn
1778-7254pii
S1297-319X(07)00390-9journal_volume
75pub_type
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