AUTOIMMUNE IDIOPATHIC THROMBOCYTOPENIC PURPURA WITH THE SUBSEQUENT OCCURRENCE OF SYSTEMIC LUPUS-ERYTHEMATOSUS

Citation
Mj. Hepburn et al., AUTOIMMUNE IDIOPATHIC THROMBOCYTOPENIC PURPURA WITH THE SUBSEQUENT OCCURRENCE OF SYSTEMIC LUPUS-ERYTHEMATOSUS, Cutis, 60(4), 1997, pp. 185-187
Citations number
20
Categorie Soggetti
Dermatology & Venereal Diseases
Journal title
CutisACNP
ISSN journal
00114162
Volume
60
Issue
4
Year of publication
1997
Pages
185 - 187
Database
ISI
SICI code
0011-4162(1997)60:4<185:AITPWT>2.0.ZU;2-1
Abstract
Cutaneous manifestations of petechiae, purpura, and ecchymosis can lea d the physician to discover an underlying platelet abnormality, Autoim mune idiopathic thrombocytopenic purpura (AITP) is a diagnosis of excl usion, mediated by a destructive IgG antibody response to the platelet s' membrane components, In addition to showing evidence of cutaneous a nd mucosal bleeding tie, epistaxis, hematuria), patients with AITP are at an increased risk for systemic lupus erythematosus (SLE), Therefor e, it is suggested that patients with AITP be closely monitored for SL E.