Menu

IDIOPATIK TROMBOSITOPENIA PURPURA EPUB

0 Comment

Idiopathic thrombocytopenic purpura (ITP) is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause. ITP (Idiopatik Trombositopenia Purpura) – Download as Powerpoint Presentation .ppt /.pptx), PDF File .pdf), Text File .txt) or view presentation slides online. Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease .. Purwanto I. Purpura trombositopenia idiopatik. In: Sudoyo AW.

Author: Jull Malalrajas
Country: Lesotho
Language: English (Spanish)
Genre: Automotive
Published (Last): 5 December 2016
Pages: 402
PDF File Size: 2.57 Mb
ePub File Size: 9.3 Mb
ISBN: 183-3-28896-637-1
Downloads: 1939
Price: Free* [*Free Regsitration Required]
Uploader: Mishakar

Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic. People with ITP should not take idiopatik trombositopenia purpura, ibuprofen, or warfarin, because these drugs interfere with platelet function or blood trombositopeia, and bleeding may occur.

What would you like to print? Management of immune thrombocytopenic purpura in pregnancy. Immune thrombocytopenia [1] ITP idiopatik trombositopenia purpura a type of ixiopatik purpura defined as isolated low platelet count thrombocytopenia with normal bone marrow and the absence of other causes of thrombocytopenia. ITP may be either acute or chronic. Anti-D immunoglobulin treatment for thrombocytopenia associated with primary antibody deficiency.

Recurrent idiopathic thrombocytopenic purpura in childhood. Platelet transfusions may be required to control clinically significant bleeding but are not recommended for prophylaxis. Practice Essentials Immune thrombocytopenic purpura ITP is a clinical syndrome in idiopatik trombositopenia purpura trombositopenia purpura a decreased number of circulating platelets thrombocytopenia see the image below manifests as a bleeding tendency, easy bruising purpuraor extravasation of blood from capillaries into skin and mucous membranes petechiae.

Most Related  SINDROME DE CRI DU CHAT PDF

August 24, ; Accessed: On examination of the bone marrow, an increase in the production of megakaryotes is seen and can help in determining ITP. The idiopatik trombositopenia purpura macrophage system idiopatik trombositopenia purpura the spleen is responsible for removing platelets in ITP, as demonstrated by the fact that splenectomy results in prompt restoration of normal platelet counts in idiopatik trombositopenia purpura patients with ITP.

Platelets are sequestered and destroyed by mononuclear macrophages, which are neither reticular nor endothelial in origin. According to studies in Denmark and England, childhood Idiopatik trombositopenia purpura occurs in approximately cases per 1, per year. Received salary from Medscape for employment. The evolution of drug discovery: Influence of the American Society of Hematology guidelines on the management of newly diagnosed childhood immune thrombocytopenia.

Bleeding complications in immune thrombocytopenia. Trombositopeina Email Print Feedback Close. Initial treatment of immune thrombocytopenic purpura with high-dose dexamethasone. The diagnosis of ITP is in part one of exclusion, requiring that other causes of thrombocytopenia be ruled out. In adults, the peak prevalence is from years of age.

Pregnant women require special consideration for delivery, as follows [ 18 ]:. Hemorrhage represents the most serious complication; intracranial trombositoprnia is the most significant.

Idiopathic thrombocytopenic purpura

Anti-platelet autoantibodies in a pregnant woman with ITP will attack the patient’s iiopatik platelets and will also cross the placenta and react against fetal idiopatik trombositopenia purpura. Bussel JB, et al. However, while sometimes effective, it is costly and produces improvement that generally lasts less than a month.

Most Related  SCWCD HANUMANT DESHMUKH PDF

Oral idiopatik trombositopenia purpura, IV methylprednisolone, or high-dose dexamethasone may be used [ 91011 ].

PATOFISIOLOGI IDIOPATIK (IMUN) TROMBOSITOPENIA PURPURA (ITP)

Chalmers S, Tarantino MD. Uses authors parameter Hrombositopenia medical condition new All articles lacking reliable references Idiopatik trombositopenia purpura lacking reliable references from July Freckles lentigo melasma nevus melanoma.

Influence of the American Society of Hematology guidelines on the management of newly diagnosed childhood immune thrombocytopenia.

The initial treatment of ITP includes: The IgG autoantibodies are also thought to damage megakaryocytesthe precursor cells to platelets, although this is believed to contribute only slightly to the decrease in platelet numbers. Long-term responses seen with rituximab in patients with ITP. Despite the destruction of idiopatik trombositopenia purpura by splenic macrophages, the spleen is normally not enlarged.

American Society of Hematology. Background Idiopathic thrombocytopenic purpura ITPidiopatik trombositopenia purpura known as primary immune thrombocytopenic purpura and autoimmune thrombocytopenic purpura, is defined as isolated thrombocytopenia with normal bone marrow and in the absence of other causes of thrombocytopenia.

Laparoscopic splenic procedures in children: This is an open-access article distributed under the terms of the Creative Idiopatik trombositopenia purpura Attribution-Noncommercial-Share Alike 3. Treating immune thrombocytopenic purpura and preventing Rh alloimmunization using intravenous rho D immune globulin.