IDIOPATIK TROMBOSITOPENIA PURPURA ADALAH PDF

Immune thrombocytopenia (ITP) is a type of thrombocytopenic purpura defined as isolated low platelet count (thrombocytopenia) with normal bone marrow and. Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease .. Purwanto I. Purpura trombositopenia idiopatik. In: Sudoyo AW. Idiopathic thrombocytopenic purpura (ITP) or immune thrombocytopenic purpura is a disease Purwanto I. Purpura trombositopenia idiopatik.

Author: Tezilkree Mak
Country: Panama
Language: English (Spanish)
Genre: Software
Published (Last): 18 March 2006
Pages: 297
PDF File Size: 13.16 Mb
ePub File Size: 14.76 Mb
ISBN: 666-4-29804-647-4
Downloads: 62269
Price: Free* [*Free Regsitration Required]
Uploader: Matilar

General care includes explaining ITP to the patient and advising him or her to watch for bruising, petechiae, or other signs of recurrence.

No lab test can reliably predict if neonatal thrombocytopenia will occur. Idiopathic thrombocytopenic purpura ITP is the condition of having a low platelet count thrombocytopenia of no known cause idiopathic.

With treatment, the chance of remission a symptom-free period is good. Splenectomy is sometimes undertaken, as platelets targeted for destruction will often meet their fate in the spleen. Journal Statistics View My Stats. The diagnosis of ITP is a diagnosis of exclusion.

IDIOPATIK TROMBOSITOPENIA PURPURA PDF

National Center adxlah Biotechnology InformationU. ITP is usually chronic in adults [40] and the probability of durable remission is 20—40 percent. Assessment of antithrombocyte antibody may assist in establishing the diagnosis of ITP. Thrombopoietin and platelet production in chronic immune thrombocytopenia. In recent years, dapsone has also proved helpful diiopatik treating lupus, rheumatoid arthritis and as a second-line treatment for ITP.

  IL GIOCO DELLA MANTIDE PDF

With epidermal involvement Eczematous contact dermatitis atopic dermatitis seborrheic dermatitis stasis dermatitis lichen simplex chronicus Darier’s disease glucagonoma syndrome langerhans cell histiocytosis lichen sclerosus pemphigus foliaceus Wiskott—Aldrich syndrome Zinc deficiency. Two distinct clinical syndromes manifest as an acute condition in children and a chronic condition in adults.

Immune thrombocytopenic purpura (ITP)

A report of 66 cases. Footnotes Source of Support: Sekhon SS, Roy V.

The latter examination in ITP shows low numbers of normal-sized platelets, occasionally also giant platelets, while erythrocytes and leukocytes have a normal morphology. Chemistry of Plants That Changed the World.

The antibodies attach to ifiopatik platelets. Immune thrombocytopenia [1] ITP is a type of thrombocytopenic purpura defined as isolated low platelet count thrombocytopenia with normal bone marrow and the absence of other causes of thrombocytopenia. The risk of neonatal thrombocytopenia is increased with: Initial clinical trials show it to be effective in chronic ITP.

Conclusion The initial treatment of ITP includes: Open in a separate window. Although most cases are asymptomatic, very low platelet counts can lead to a bleeding diathesis and purpura. Red Blanchable Erythema Generalized drug eruptions viral exanthems toxic erythema systemic lupus erythematosus.

  HERMANN HESSE NARZISS UND GOLDMUND PDF

The size and appearance of the platelets may be abnormal. Please review our privacy policy.

People with the disease have too few platelets in the blood. Idiopathic thrombocytopenic purpura ITP is defined as a hematologic disorder, characterized by isolated thrombocytopenia without a clinically apparent cause.

Idiopathic thrombocytopenic purpura

The patient was followed-up for 2 years and there was no re-occurence reported. There is no specific treatment for ITP. There is no accepted platelet count that defines an indication for initial treatment.

Cellular immune mechanisms in autoimmune thrombocytopenic purpura: Retrieved October 16,