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Síndrome antifosfolípico: primario y secundario

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Síndrome antifosfolípico: primario y secundario

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Quiz sobre APS primario y APS asociado

Created by

Magally Escobar
Magally Escobar
Colombia

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Síndrome antifosfolípico: primario y secundario
 

Síndrome antifosfolípico: primario y secundarioOnline version

Quiz sobre APS primario y APS asociado

by Magally Escobar
1

¿Qué define principalmente al síndrome antifosfolípido (APS)?

2

¿Qué marcadores se buscan en el laboratorio para APS?

3

¿Qué diferencia al APS primario del secundario?

4

¿Cuál es una complicación obstétrica típica del APS?

5

¿Qué evento trombótico es frecuente en APS?

6

¿Qué manejo es fundamental en APS?

7

¿Qué factor de riesgo modifica el diagnóstico de APS secundario?

8

¿Qué criterio NO es parte de la clasificación clínica de APS?

9

¿El APS puede presentarse sin trombosis?

10

¿Qué prueba de laboratorio es útil para confirmar APS a largo plazo?

Explicación

APS es un trastorno autoinmune con trombosis y problemas obstétricos, no una infección ni deficiencia de anticuerpos.

Los tres marcadores clave son lupus anticoagulant, anticardiolipina y anti-β2GPI.

Primario no está relacionado con otra enfermedad autoinmune; secundario sí con SLE u otras patologías.

APS puede causar aborto espontáneo recurrente o morbilidad obstétrica como parto prematuro.

La trombosis puede ser venosa o arterial; la hemorrágica no es típica como presentación inicial.

La base es anticoagulación; antihistamínicos no son tratamiento principal.

APS secundario se asocia a SLE u otros trastornos autoinmunes.

La trombocitopenia puede ocurrir pero no es criterio clínico principal sin contexto trombótico.

Puede presentarse con embarazo complicado o sólo con marcadores, sin trombosis.

La persistencia de marcadores antifosfolípidos en el tiempo ayuda a confirmar APS.

 
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