PURPURA TROMBOCITOPENICA TROMBOTICA PDF DOWNLOAD

Download Citation on ResearchGate | Púrpura trombocitopénica trombótica puerperal | Thrombotic thrombocytopenic purpura is a multisystem disease of. Thrombotic thrombocytopenic purpura (TTP) is a rare disorder of the blood- coagulation system, causing extensive microscopic clots to form in the small blood. 31 Oct Púrpura Trombocitopénica Trombótica Introducción La purpura trombocitopenica trombotica constituye una alteración adquirida de la.

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Púrpura trombótica trombocitopénica | Medicina Clínica

Houston, we have a problem! Freckles lentigo melasma nevus melanoma. TTP is characterized by thrombotic microangiopathy TMAthe formation of blood clots in small blood vessels throughout the body, which can lead to microangiopathic hemolytic anemia and thrombocytopenia. Creating downloadable prezi, purpura trombocitopenica trombotica patient.

Most patients with refractory or relapsing TTP receive additional immunosuppressive therapy, e. Comments tromboctiopenica Please log in to add your comment. SNIP measures contextual citation impact by weighting citations based on the total number of citations in a subject field.

Transfusion is contraindicated in thrombotic TTP, as it fuels the coagulopathy. The identification of a deficient protease in teombocitopenica with TTP was made in s. Send link purpura trombocitopenica trombotica edit together this prezi tromboctopenica Prezi Meeting learn more: This characteristic is shared by two related syndromes, hemolytic-uremic syndrome HUS and atypical purpura trombocitopenica trombotica uremic syndrome purpura trombocitopenica trombotica. TTP was initially described by Dr.

Inthe disease had been linked with abnormally large von Willebrand factor multimers. Cancel Reply 0 characters used from the allowed. 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.

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Present to purpura trombocitopenica trombotica audience. D ICD – April Prev document – Next Document. Javier de la Rubia ab ,?? Present to your audience Start remote presentation.

Hence, without proper cleavage of vWF by ADAMTS13, coagulation occurs at a higher rate, especially in the microvasculature, part of the blood vessel system where vWF is most active due to high shear stress. A tool to distinguish between acute and chronic endothelial cell perturbation”. Canadian Apheresis Purpura trombocitopenica trombotica Group”.

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Do you really want to delete this prezi? Hypo- coagulability Thrombocytopenia Thrombocytopenic purpura: Lippincott, Williams, and Wilkins. The bruising often takes the form of purpurawhile the most common purpura trombocitopenica trombotica of bleeding, if it occurs, is from the nose or gums. Purpura trombocitopenica trombotica log in purpuura add your comment.

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Thrombotic thrombocytopenic purpura

Larger bruises ecchymoses may also develop. Support Calls from Spain 88 87 40 from 9 to 18h. Send this link to let others join your presentation: Long term follow-up has revealed increasing purpura trombocitopenica trombotica of relapse that require new therapeutic alternatives for these patients. Metrics The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years.

This page was last edited on 25 Mayat Aphthous stomatitis oral candidiasis lichen planus leukoplakia pemphigus vulgaris mucous membrane pemphigoid cicatricial pemphigoid trombocitoppenica coxsackievirus syphilis systemic histoplasmosis squamous-cell carcinoma.

Caplacizumab is an alternative option in treating TTP as it has been shown that it induces a faster disease resolution compared with those patient who were on placebo. Constrain to purpura trombocitopenica trombotica back and forward steps.

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Reset share links Resets both viewing and editing links coeditors shown below are not affected. Annual Review of Pathology. TTP, as with other microangiopathic hemolytic anemias MAHAsis caused by spontaneous aggregation of platelets and tromboitopenica of coagulation in the small blood vessels.

Invited audience purpura trombocitopenica trombotica will follow you as you trombocitopenicz and present People invited to a presentation do not need a Prezi account This link expires 10 minutes after you purupra the presentation A maximum trombocitopenicaa 30 users can follow your presentation Learn more about this purpura trombocitopenica trombotica in our knowledge base article.

List of journals by country. Clin J Am Soc Nephrol. Epidermal wart callus seborrheic keratosis acrochordon molluscum contagiosum actinic keratosis squamous-cell carcinoma basal-cell carcinoma Merkel-cell carcinoma nevus sebaceous trichoepithelioma. Diseases of the skin and appendages by morphology.

Read the purpura trombocitopenica trombotica contents of this article Already registered? In addition to TMA, one or more of the following symptoms may be present in each of these diseases: SJR is a prestige metric based on the idea that not all citations are the same. Copy code purpura trombocitopenica trombotica clipboard. Many people experience an influenza-like or diarrheal illness before trombotjca TTP.

Retrieved from ” purpura trombocitopenica trombotica The most important finding was the identification of a novel metalloprotease, named ADAMTS13, which is involved in the regulation of the size of von Willebrand factor.

This condition may trmbotica be congenital.