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		<title>Antiphospholipid syndrome - 修訂歷史</title>
		<link>http://owiki.kmu.edu.tw/index.php?title=Antiphospholipid_syndrome&amp;action=history</link>
		<description>本站上此頁的修訂歷史</description>
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			<title>Guhjy: 新頁面: *Antibody to anionic phospholipids, particularly ''&amp;beta;2 glycoprotein 1'' *Diagnostic criteria **Presence in the serum of at least one type of autoantibody known as an antiphospholipid ...</title>
			<link>http://owiki.kmu.edu.tw/index.php?title=Antiphospholipid_syndrome&amp;diff=24424&amp;oldid=prev</link>
			<description>&lt;p&gt;新頁面: *Antibody to anionic phospholipids, particularly ''&amp;amp;beta;2 glycoprotein 1'' *Diagnostic criteria **Presence in the serum of at least one type of autoantibody known as an antiphospholipid ...&lt;/p&gt;
&lt;p&gt;&lt;b&gt;新頁面&lt;/b&gt;&lt;/p&gt;&lt;div&gt;*Antibody to anionic phospholipids, particularly ''&amp;amp;beta;2 glycoprotein 1''&lt;br /&gt;
*Diagnostic criteria&lt;br /&gt;
**Presence in the serum of at least one type of autoantibody known as an antiphospholipid antibody, which is directed against phospholipid-binding plasma proteins&lt;br /&gt;
**The occurrence of at least one clinical feature from a diverse list of potential disease manifestations, the most common of which are categorized as venous or arterial thromboses, pregnancy morbidity, or thrombocytopenia&lt;br /&gt;
*Idiopathic, pregnancy, hemodialysis, RT, GN (minimal change disease, membranous nephropathy), SLE (lupus anticoagulant with activated partial tissue thromboplastin time &amp;amp;uarr;)&lt;br /&gt;
*Clinical features&lt;br /&gt;
**Hematuria, proteinuria&lt;br /&gt;
**[[Vasculitis]]&lt;br /&gt;
***Treated by corticosteroids&lt;br /&gt;
**Severe form: hemolytic anemia, deep vein thrombosis, transient ischemic attacks, pulmonary embolism, spontaneous abortions&lt;br /&gt;
***&amp;lt;10% present have catastrophic multi-organ involvement and acute renal failure&lt;br /&gt;
***''Patients who present with acute flank pain and renal vein thrombosis in the setting of proteinuria should always be checked for antiphospholipid antibodies''&lt;br /&gt;
**Less severe form&lt;br /&gt;
**P'ts can wax and wane, and many patients have recurrences&lt;br /&gt;
*Thrombotic microangiopathy of the kidneys (25%)&lt;br /&gt;
**Affects interlobular artery, arterioles and glomerular capillaries&lt;br /&gt;
**Microthrombi&lt;br /&gt;
**Endotheliosis (also seen in preeclampsia/HELLP [hemolysis, elevated liver enzymes, and low platelet count syndrome], malignant hypertension)&lt;br /&gt;
**Treatment&lt;br /&gt;
***Warfarin&lt;br /&gt;
***[[Plasmapheresis]] and immunosuppresives for acute renal failure&lt;/div&gt;</description>
			<pubDate>Tue, 13 Mar 2018 09:47:06 GMT</pubDate>			<dc:creator>Guhjy</dc:creator>			<comments>http://owiki.kmu.edu.tw/index.php/Talk:Antiphospholipid_syndrome</comments>		</item>
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