A CASE OF IDIOPATHIC THROMBOCYTOPENIC PURPURA PRESENTING MENTAL SIGNS AND GENERAL CLONIC SPASM
نویسندگان
چکیده
منابع مشابه
Bernard-Soulier syndrome or idiopathic thrombocytopenic purpura: A case series
Background: Bernard-Soulier syndrome (BSS) is a rare, autosomal recessive platelet function disorder which is commonly mistaken for idiopathic thrombocytopenic purpura (ITP).The report includes seven cases of BSS that have been diagnosed and treated as ITP for a long time. Methods: Between 2006 and 2016, data of seven BSS patients who have long been diagnosed and treated as ITP were collected ...
متن کاملHodgkin's disease presenting as "idiopathic" thrombocytopenic purpura.
A case of Hodgkin's disease presenting as idiopathic thrombocytopenic purpura in a 23-year-old male is reported. This is a rare presentation of Hodgkin's disease having been previously described in only two cases.
متن کاملEpidemiology of Idiopathic Thrombocytopenic Purpura in Children
Abstract Background Immune thrombocytopenic purpura (ITP) is a common autoimmune bleeding condition in children that is characterized by a decrease in the platelet count. The aims of this study were to define epidemiologic features of patients with primary ITP who were admitted to Mofid Children's Hospital, Tehran, Iran, in a 5-year period. Methods We retrospectively studied the records of ...
متن کاملA Case Study of Silent Thyroiditis Associated with Idiopathic ُThrombocytopenic Purpura
A 48 Year-old woman had symptoms of thyrotoxicosis which disappeared spontaneously within two months. She was diagnosed as case of silent thyroiditis on the basis of both the clinical course and the laboratory data such as low uptake of radioactive Iodine and Technesium. She also had petechia in her arms which were diagnosed as an idiopathic thrombocytopenic purpura (I.T.P.). This case would se...
متن کاملPrimary Splenic Angiosarcoma Presenting as Idiopathic Thrombocytopenic Purpura: A Case Report and Review of the Literature
Angiosarcoma of the spleen is a rare malignancy that arises from vascular endothelial origin. This neoplasm is highly malignant and diagnosis is often delayed due to the vague presentation of clinical symptoms. A case report and concise review of the current diagnostic criteria and surgical treatment are provided to aid in the detection and treatment of this malignancy. We present a case of a 5...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Nihon Naika Gakkai Zasshi
سال: 1965
ISSN: 0021-5384,1883-2083
DOI: 10.2169/naika.54.940