Rare association of a patient with multiple ischemic strokes with thrombotic thrombocytopenic purpura and systemic lupus erythematosus: A case report
نویسندگان
چکیده
The Trial of ORG 10172 in Acute Stroke Treatment categorizes stroke etiology into large artery atherosclerosis, small vessel occlusion, cardio embolism, undetermined etiology, and other determined with patients hematological, hypercoagulable states falling under the last category.
منابع مشابه
[Thrombotic thrombocytopenic purpura in a patient with systemic lupus erythematosus].
Thrombotic thrombocytopenic purpura (TTP) is a rare dynamic life-threatening disease with systemic formation of platelet thrombi in the microvasculature within all the organs. Until recently the mortality in TTP has exceeded 90%. The progress of medical research in the last two decades has significantly improved our understanding of the pathogenesis of TTP and allowed a reduction in mortality. ...
متن کاملThrombotic thrombocytopenic purpura in a child with systemic lupus erythematosus.
We report a child with thrombotic thrombocytopenic purpura (TTP) secondary to systemic lupus erythematosus. The diagnosis was confirmed by low ADAMTS13 activity (<5%) along with the presence of a low titer inhibitor. Her clinical course was complicated by systemic lupus erythematosus, immunosuppressant therapy, and septic shock. She responded to plasma exchange and ADAMTS13 activity levels reco...
متن کاملThrombotic thrombocytopenic purpura and systemic lupus erythematosus.
We report two patients with systemic lupus erythematosus who subsequently developed thrombotic thrombocytopenic purpura. In each case the coexistence of these two conditions was confirmed by pathological findings. Both patients responded to treatment, but one eventually died. A review of the literature suggests a possible relationship between the two disorders.
متن کامل[Systemic lupus erythematosus and thrombotic thrombocytopenic purpura].
JAPI • VOL. 51 • JULY 2003 smear shows red cell fragments, schistocytes, and helmet cells suggestive of hemolysis. Other features suggestive of MAHA are reticulocytosis, indirect hyperbilirubinina, hemoglobinuria, nucleated red cells and increased LDH. Coagulation parameters are normal except increased FDP. Histopathology shows hyaline thrombi and microthrombi in arterioles and capillaries. Mor...
متن کاملThrombotic thrombocytopenic purpura preceding systemic lupus erythematosus.
The case of a patient admitted with thrombotic thrombocytopenic purpura nine years after developing systemic lupus erythematosus (SLE) is reported. Thrombotic thrombocytopenic purpura associated with SLE has been described on other occasions, but in most patients the diagnosis of SLE precedes that of thrombotic thrombocytopenic purpura. The unusual sequence and the chronological separation of t...
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ژورنال
عنوان ژورنال: Journal of clinical images and medical case reports
سال: 2023
ISSN: ['2766-7820']
DOI: https://doi.org/10.52768/2766-7820/2346