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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Fibrillary_glomerulonephritis</id>
	<title>Fibrillary glomerulonephritis - Revision history</title>
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	<updated>2026-04-26T12:34:46Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://wikimd.org/index.php?title=Fibrillary_glomerulonephritis&amp;diff=2153616&amp;oldid=prev</id>
		<title>Deepika vegiraju: Created page with &quot;&#039;&#039;&#039;Other Names:&#039;&#039;&#039; Non-amyloid fibrillary glomerulopathy; Congo red-negative amyloidosis-like glomerulopathy; Non-amyloid fibrillary glomerulonephritis  Fibrillary glomerulone...&quot;</title>
		<link rel="alternate" type="text/html" href="https://wikimd.org/index.php?title=Fibrillary_glomerulonephritis&amp;diff=2153616&amp;oldid=prev"/>
		<updated>2020-11-10T17:29:07Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;&amp;#039;&amp;#039;&amp;#039;Other Names:&amp;#039;&amp;#039;&amp;#039; Non-amyloid fibrillary glomerulopathy; Congo red-negative amyloidosis-like glomerulopathy; Non-amyloid fibrillary glomerulonephritis  Fibrillary glomerulone...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;&amp;#039;&amp;#039;&amp;#039;Other Names:&amp;#039;&amp;#039;&amp;#039; Non-amyloid fibrillary glomerulopathy; Congo red-negative amyloidosis-like glomerulopathy; Non-amyloid fibrillary glomerulonephritis&lt;br /&gt;
&lt;br /&gt;
Fibrillary glomerulonephritis is an uncommon cause of [[glomerular]] disease. A more rare disorder known as immunotactoid [[glomerulpathy]] is a very similar condition. Both disorders probably result from deposits derived from [[immunoglobulins]] but in most cases the cause is idiopathic (unknown).&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Cause&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Both fibrillary glomerulonephritis and immunotactoid glomerulopathy have been associated with [[hepatitis C]] virus infection and with malignancy and [[autoimmune disease]]. Because of this, patients should be screened for these conditions.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Signs and symptoms&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
The signs and symptoms include blood ([[hematuria]]) and protein ([[proteinuria]]) in the urine, kidney insufficiency and high blood pressure.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Diagnosis&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
The diagnosis is made with a kidney [[biopsy]] and by [[electron microscopy]]. Fibrillary glomerulonephritis and immunotactoid glomerulopathy can be differentiated from each other by electron microscopy; the fibrils in fibrillary glomerulonephritis are smaller and randomly oriented as opposed to the larger and often organized fibrils of immunotactoid glomerulopathy.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Treatment&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
Treatment is generally determined by the severity of the kidney problems.&lt;br /&gt;
The most common form of treatment was [[steroids]], with or without a second agent, including most notably [[cyclophosphamide]] or [[rituximab]]. A benefit of [[immunosuppression]] could not be detected in these small, retrospective studies in which patients with more severe disease were more likely to have been treated.&lt;br /&gt;
&lt;br /&gt;
== &amp;#039;&amp;#039;&amp;#039;Prognosis&amp;#039;&amp;#039;&amp;#039; ==&lt;br /&gt;
The prognosis for patients with FGN remains poor, with limited data to suggest optimal therapy.&lt;br /&gt;
&lt;br /&gt;
{{rarediseases}}&lt;br /&gt;
{{stub}}&lt;/div&gt;</summary>
		<author><name>Deepika vegiraju</name></author>
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