Idiopathic thrombocytopenic purpura pathophysiology: Difference between revisions

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'''AA:'''<ref name="pmid183290874">{{cite journal |vauthors=Elias PM, Hatano Y, Williams ML |title=Basis for the barrier abnormality in atopic dermatitis: outside-inside-outside pathogenic mechanisms |journal=J. Allergy Clin. Immunol. |volume=121 |issue=6 |pages=1337–43 |date=June 2008 |pmid=18329087 |pmc=2706021 |doi=10.1016/j.jaci.2008.01.022 |url=}}</ref>
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==References==
==References==
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Revision as of 18:08, 1 November 2018

Idiopathic thrombocytopenic purpura Microchapters

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Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Idiopathic thrombocytopenic purpura from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

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Risk calculators and risk factors for Idiopathic thrombocytopenic purpura pathophysiology

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Pathophysiology

Physiology

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Pathogenesis

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Genetics

Associated Conditions

Conditions associated with

Gross Pathology

On gross pathology, characteristic findings of itp include:

  • Acute atopic dermatitis:
  • Chronic atopic dermatitis:

Microscopic Pathology

On microscopic histopathological analysis, characteristic findings of itp include:

  • Acute vesicular lesions:
  • Chronic lichenified plaque:

References

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References

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