Jn. George et Ge. Raskob, IDIOPATHIC THROMBOCYTOPENIC PURPURA - DIAGNOSIS AND MANAGEMENT, The American journal of the medical sciences, 316(2), 1998, pp. 87-93
Idiopathic thrombocytopenic purpura (ITP, also known as immune thrombo
cytopenic purpura) in adults is principally a disease of young women.
Although in some patients the onset is acute and complete resolution o
ccurs, in most patients, the onset is insidious and the course is chro
nic. In spite of the relative frequency of ITP, there are important un
resolved issues in its diagnosis and management. For this reason, the
American Society of Hematology (ASH) chose ITP as the disease topic fo
r its initial sponsored practice guideline in 1993. A major conclusion
of the published guideline was the lack of firm evidence on which to
base diagnostic procedures and management strategies. This review desc
ribes the clinical features of ITP in adults, emphasizes the principal
unresolved issues in diagnosis and management, and outlines the criti
cal areas for future research.