Pdf thrombotic thrombocytopenic purpura concomitant with. Purpura trombocitopenica trombotica plaqueta endotelio. Diagnostic and treatment guidelines for thrombotic. Thrombotic thrombocytopenic purpura ttp hematology and. The immune system destroys platelets, which are necessary for normal blood clotting. A peripheralblood smear showed numerous schistocytes, and a diagnosis of thrombotic thrombocytopenic purpura. Purpura trombositopenik trombotik ttp jarang dijumpai dan ditandai dengan trombositopenia, anemia hemolitik mikroangiopati, kelainan neurologi yang berfluktuasi, sering ditandai dengan demam dan gangguan ginjal. Trombotik trombositopenik purpura ttp ve hemolitik uremik sendrom hus bu bolumde soz konusu edeceimiz trombositopeni sebeple ridir. Thrombotic thrombocytopenic purpura associated with pregnancy. Ttp is a rare lifethreatening disease, characterized by maha, thrombocytopenia, fever, renal involvement and neurologic. Signs and symptoms typically develop in infancy or early childhood, but in some cases they do not develop until adulthood, particularly during pregnancy in women or after an infection or vaccination. Pdf thrombotic thrombocytopenic purpura is charactarized by microangiopathic hemalitic anemia, thromboctopenia, fever, neurologic abnormailities and.
This guide is also included in the medsurg bundle your purchase will give you a. Thrombotic thrombocytopenic purpura ttp and hemolyticuremic syndrome hus are two important acute conditions to diagnose. In its fullblown form, the disease consists of the following pentad. An openlabel, unit dosefinding study of amg 531, a novel thrombopoiesisstimulating peptibody, in patients with immune thrombocytopenic purpura. Some women may have heavier or longer periods or breakthrough bleeding. Survival and relapse in patients with thrombotic thrombocytopenic purpura.
Bruising, particularly purpura in the forearms and petechiae in the feet, legs, and mucous membranes, may be caused by spontaneous bleeding under the skin. Patients with thrombotic thrombocytopenic purpura ttp can present with devastating neurological abnormalities. Typically, its appearance in the saqs is either accompanied by a pair of diseasedlooking legs. Trombocitopenia amegacariocitica congenita femexer. The prompt recognition and treatment of this disease process. Diagnosis and management of thrombotic thrombocytopenic. Immune thrombocytopenic purpura itp telah mengalami perubahan definisi dan klasifikasi. Persons with the disease have too few platelets in the blood. Gebelerde trombositopeni %48 gestasyonel trombositopeni 12 dogum immun trombositopeni izlenir antikorlar. Thrombotic thrombocytopenic purpura ttp is an unusual disease manifested clinically by hemolytic anemia, thrombocytopenia, fever, renal involvement and neurologic manifestations, and characterized pathologically by occlusion of small blood vessels in many organs by an homogenous, eosinophilic matter. Historically, nearly all patients died during the first month of illness with severe hemolytic anemia, abundant schistocytes, profound thrombocytopenia, neurological deficits, renal injury, and fever.
Thrombocytopenic thrombotic purpura ttp is a severe hemorrhagic syndrome characterized by thrombocytopenia, microangiopathic hemolytic anemia and microvascular occlusion, besides the associated symptoms that may or may not be. Pathophysiology of thrombotic thrombocytopenic purpura. Almost 80 years after eli moschcowitz published the first description of the disease, most patients with idiopathic thrombotic thrombocytopenic purpura ttp were found to have acquired autoantibody inhibitors of the adamts metalloprotease. Acquired thrombotic thrombocytopenic purpura must meet all. Itp is sometimes called immune thrombocytopenic purpura or simply, immune thrombocytopenia. For more than a halfcentury after its initial recognition, mortality was near 100% and the etiology totally obscure. Makalah penyakit idiopatik tombositopeni purpura satya.
Trombotik trombositopenik purpura trombotik thrombositopenik purpura ttp, mikroanjiopatik hemolitik anemi, trombositopeni, ates, bobrek yetmezligi ve norolojik bulgularla karakterizetir. Media in category thrombotic thrombocytopenic purpura the following 5 files are in this category, out of 5 total. Thrombotic thrombocytopenic purpura ttp is a rare, idiopathic, acute, systemic coagulopathy characterized by platelet consumption and thrombus formation in small vessels. Until recently, ttp has mainly been diagnosed by clinical findings such as thrombocytopenia and nonimmune hemolytic anemia. Thrombotic thrombocytopenic purpura is a rare disorder that causes blood clots thrombi to form in small blood vessels throughout the body. Lindungi dari luka yang dapaet menyebabkan memar atau perdarahan, lakukan terapi yang benar untuk infeksi yang mungkin dapat. Immune thrombocytopenia purpura itp, also known as idiopathic thrombocytopenic purpura, is a type of thrombocytopenic purpura defined as an isolated low platelet count with a normal bone marrow in the absence of other causes of low platelets.
Ttp occurs at any age with a peak incidence in the third decade of life and a female to male preponderance of 3. A 60yearold woman with fever, lassitude, neurological symptoms, hematuria, subconjunctival bleeding, several ecchymoses, reticulocytosis, microangiopathic hemolytic anemia with burr cells, schistocytes, and spherocytes, and thrombocytopenia was first seen in the neurology clinic in 1985. Thrombotic thrombocytopenic purpura ttp can rapidly progress into a lifethreatening condition, thus the importance of appropriate diagnosis and treatment cannot be overstated. Thrombotic thrombocytopenic purpura is suspected in patients with suggestive symptoms, thrombocytopenia, and anemia. This leads to a low platelet count thrombocytopenia. A peripheralblood smear showed numerous schistocytes, and a diagnosis of thrombotic thrombocytopenic purpura was made. Thrombocytopenic thrombotic purpura ttp is a rare etiology in critically ill patients 0. It is a condition in, which there is bruising purpura because there are fewer platelets in the blood than usual. Trombotik trombositopenik purpura ttp mikroanjiopatik hemolitik anemi, trombositopeni, ates, norolojik bulgular ve bobrek yetmezligi ile karakterize, hayat. Direncli bir trombotik trombositopenik purpura olgusunda rituksimab.
Autoimmune hemolytic anemia and thrombocytopenia megaloblastic anemia due to vitamin b12 or folic acid deficiency. Pdf thrombotic thrombocytopenic purpura ttp is characterized by. Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies. In ttp, blood clots form in small blood vessels throughout the body. Acquired ttp is mainly idiopathic, but there are other conditions and comorbidities besides idiopathic. Mata retinitis kulit livido retikularis, gangren superfisial, purpura, ekimosis, nodul subkutan jantung. Idiopathic thrombocytopenia purpura is a blood disorder affecting the platelets. Ttphus comes up remarkably often in the fellowship exam.
Thrombotic thrombocytopenic purpura ttp is a clearly defined entity of thrombotic microangiopathies tmas, a heterogeneous group of disorders characterized by microangiopathic hemolytic anemia. Congenital thrombotic thrombocytopenic purpura congenital ttp is a blood disorder in which blood clots form in the small blood vessels throughout the body. Menghindari obatobatan seperti aspirin atau ibuprofen yang dapat mempengaruhi platelet dan meningkatkan resiko perdarahan. The clots can limit or block the flow of oxygenrich blood to the bodys organs, such as the brain, kidneys, and heart. A case of acquired thrombotic thrombocytopenic purpura. Thrombotic thrombocytopenic purpura wikimedia commons. We present a case report of acute ttp following a bout of ischemic colitis. Enable javascript to view the expandcollapse boxes. Pdf trombotik trombositopenik purpura researchgate.
Immune thrombocytopenic purpura, itp is an autoimmune bleeding disorder. This results in a low platelet count, low red blood cells due to their breakdown, and often kidneys, heart, and brain dysfunction. It is an important diagnosis to make because the untreated mortality is 90%, which can be reduced with the prompt delivery of plasma exchange pex. Thrombotic thrombocytopenic purpura ttp is a rare blood disorder characterized by clotting in small blood vessels thromboses, resulting in a low platelet count. Previously received medication for the covered indication or member has previously. Diagnosis and management of thrombotic thrombocytopenic purpura. Oct 08, 2012 idiopatik trombositopeni purpura disebut sebagai suatu gangguan autoimun yang ditandai dengan trombositopenia yang menetap angka trombosit darah perifer kurang dari 15. We are holding a free tma symposium on 5 july 2019. Update on thrombotic thrombocytopenic purpura hematology. Thrombocytopenic thrombotic purpura ttp is a severe hemorrhagic syndrome characterized by thrombocytopenia, microangiopathic hemolytic anemia and microvascular occlusion, besides the associated symptoms that may or may not be present.
These clots can cause serious medical problems if they block vessels and restrict blood flow to organs such as the brain, kidneys, and heart. A read is counted each time someone views a publication summary such as the title, abstract, and list of authors, clicks on a figure, or views or downloads the fulltext. Penanganan terkini idiopatik trombositopenia purpura itp. Thrombotic thrombocytopenic purpura ttp is rare, with a reported incidence of six cases per million per year in the uk scully et al, 2008.
Guidelines on the diagnosis and management of thrombotic thrombocytopenic purpura and other thrombotic microangiopathies article in british journal of haematology 1583. Thrombotic thrombocytopenic purpura ttp is a blood disorder that results in blood clots. Congenital ttp is a rare autosomal recessive disease present in childhood. Thrombotic thrombocytopenic purpura ttp consists of the pentad of thrombocytopenia, hemolytic anemia, fever, neurologic abnormalities, and renal disease. Thrombotic thrombocytopenic purpura ttp has long been recognized as a dire hematologic emergency. Pdf survival and relapse in patients with thrombotic. Thrombotic microangiopathic diseases thrombotic thrombocytopenic purpura ttp is categorized into acquired idiopathic ttp and congenital familial ttp. Thrombotic thrombocytopenic purpura and haemolytcuraemic syndrome are a couple of horrible problems which together with hellp and maha fall into the spectrum of thrombotic microangiopathies. A 35yearold man presented with a 2day history of abdominal pain and headache.
Thrombotic thrombocytopenic purpura, acquired genetic. Diagnostic testing for differential diagnosis in thrombotic. Genetic and rare diseases information center gard po box 8126, gaithersburg, md 208988126 tollfree. By tradition, the term idiopathic thrombocytopenic purpura is used when the cause is idiopathic. This report reminds the clinician that ischemic colitis can be an atypical presentation of ttp. Purpura trombocitopenica trombotica, diagnostico e tratamento. Ttp, mikroanjiopatik hemolitik anemi, trombositopeni. Some individuals with thrombocytopenia may experience external bleeding such as nosebleeds, andor bleeding gums. In addition to hus, the differential diagnosis also includes immune thrombocytopenic purpura itp and disseminated intravascular coagulation. Coma in thrombotic thrombocytopenic purpura journal of. Children and adults with thrombotic thrombocytopenic purpura associated with severe, acquired adamts deficiency.
The early recognition is critical because it is an emergency condition requiring urgent therapeutic plasma exchange, which is a lifesaving procedure. Another form is thrombotic thrombocytopenic purpura. Hamed 218 diagnosis and management of thrombotic thrombocytopenic purpura page 3 of 6 9 re s e pv. It is characterized by smallvessel plateletrich thrombi that cause thrombocytopenia, microangiopathic hemolytic anemia, and sometimes organ damage. Thrombotic thrombocytopenic purpura genetics home reference. Anemia, thrombocytopenia, fever, neurological signs and renal abnormalities make up the classic pentad. Thrombotic thrombocytopenic purpura deranged physiology.
Caplacizumab for acquired thrombotic thrombocytopenic purpura pdf. Thrombotic thrombocytopenic purpura ttp information for patients. J blood disord symptoms treat secondary to the thrombocytopenia purpura, ecchymosis, menorrhagia, epistaxis, hematuria, and gastrointestinal hemorrhage are also common 4. Idiopatik trombositopeni purpura itp tidak dapat dicegah, tetapi dapat dicegah komplikasinya. Penyebabnya tidak dikenal, tetapi sekitar setengah jumlah pasien mempunyai riwayat penyakit virus yang belum lama terjadi. For language access assistance, contact the ncats public information officer. Guidelines on the diagnosis and management of thrombotic. Trombotik trombositopenik purpura ttp, mikroanjiyopatik hemolitik anemi, uremi, trombositopeni, norolojik semptomlar ve atesin pentad. If the disorder is suspected, urinalysis, peripheral blood smear, reticulocyte count, serum ldh, haptoglobin, renal function tests, adamts assay, serum bilirubin direct and indirect, and direct antiglobulin test are done. Susana avila martinez purpura trombocitopenica trombotica 2.
Trombotik trombositopenik purpura, sis temik bozukluk, hemolitik anemi, trombositopeni. Consensus on the standardization of terminology in. This disease may be caused by problems with an enzyme a type of protein that is involved in blood clotting. Thrombotic thrombocytopenic purpura ttp is a rare blood disorder. Nov, 20 differential diagnosis thrombotic thrombocytopenic purpura ttp disseminated intravascular coagulation dic hus evans syndrome. Thrombotic thrombocytopenic purpura associated with graves. Idiopathic thrombocytopenia purpura itp what is idiopathic thrombocytopenia purpura or itp.
Thrombotic thrombocytopenic purpura ttp, a thrombotic microangiopathy tma, is a syndrome consisting of microangiopathic hemolytic anemia maha, thrombocytopenia, and endorgan damage secondary to microvascular thrombi. Dratwa nephrology, chu brugmann, brussels, belgium email. In addition to these clinical findings, however, reduced activity of a disintegrinlike. It is caused by a deficiency of a disintegrinlike and metalloprotease with a thrombospondin type1 motif adamts. Thrombotic thrombocytopenic purpura ttp is the most extensive and dangerous intravascular platelet clumping disorder. Purpura rentals muebles exclusivos purpura rentals. If you have problems viewing pdf files, download the latest version of adobe reader.
Trombositopenia, anemia hemolitik, sindroma hemolitik uremik, purpura trombotik trombositopeni lainlain perforasi septum nasal, nekrosis avaskular tulang 2. Thrombotic microangiopathy tma is a broad pathophysiologic process that leads to microangiopathic hemolytic anemia and thrombocytopenia, and involves capillary and small. Thrombotic thrombocytopenic purpura national heart, lung. Purpura trombocitopenica inmunologica o idiopatica. Diagnosis is done by the help of symptoms and only blood count abnormality is thrombocytopenia. Thrombotic thrombocytopenic purpura ttp is a rare and lifethreatening thrombotic microangiopathy characterized by microangiopathic hemolytic anemia, severe thrombocytopenia, and organ ischemia linked to disseminated microvascular platelet richthrombi. However, most cases are now considered to be immunemediated. Neonatal purpura definition of neonatal purpura by the free. Thrombotic thrombocytopenic purpura blood american. Thrombotic thrombocytopenic purpura ttp is a thrombotic microangiopathy, which is classically associated with signs and symptoms of fever, thrombocytopenia, neurologic deficits, hemolytic anemia, and renal failure. Purpura trombocitopenica idiopatica cancer care of western. Congenital thrombotic thrombocytopenic purpura genetic.
Nov 18, 2019 trombotik mikroanjiyopatiler tma, farkl. Thrombotic thrombocytopenic purpura ttp is a clearly defined entity of the thrombotic microangiopathies tma, a heterogeneous group of disorders characterized by microangiopathic hemolytic anemia with red cell fragmentation, thrombocytopenia and. Thrombotic thrombocytopenic purpura ttp is a rare, lifethreatening thrombotic microangiopathy which causes significant morbidity and mortality unless promptly recognized and treated. L akibat autoantibodi yang mengikat antigen trombosit menyebabkan destruksi prematur trombosit dalam sistem retikuloendotel terutama di limpa. Trombot dk trombos dtopen dk purpura gdrds trombotik trombositopenik purpura ttp ve hemolitik uremik sendrom hus mikroanjiopatik hemolitik anemi ve trombositopeni ile seyreden multipl organ sistemini etkileyen akut bir sendromdur. It causes a characteristic red or purple bruiselike rash and an increased tendency to bleed.
Thrombotic thrombocytopenic purpura ttp hus aetiology. Ttp stands for thrombotic thrombocytopenic purpura, which is a rare disorder of the blood clotting system. Thrombotic thrombocytopenic purpura ttp is a blood disorder that results in blood clots forming in small blood vessels throughout the body. Purpura trombocitopenica neonatal by zayra carachure on prezi. Sep 14, 2017 idiopatik trombositopeni purpura adalah suatu gangguan autoimun yang ditandai dengan trombositopenia yang menetap angka trombosit darah perifer kurang dari 15. Thrombotic thrombocytopenic purpura, graves disease, thrombocytopenia ozet graves hastal. Scully m et al guidelines on the diagnosis and management of thromboticscully m et al. Feb 08, 2016 purpura trombocitopenica trombotica 1. Pdf treatment of thrombotic thrombocytopenic purpura.
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