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	<id>https://wikimd.org/index.php?action=history&amp;feed=atom&amp;title=Nephroma</id>
	<title>Nephroma - Revision history</title>
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	<updated>2026-04-27T00:34:23Z</updated>
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		<id>https://wikimd.org/index.php?title=Nephroma&amp;diff=5610817&amp;oldid=prev</id>
		<title>Prab: CSV import</title>
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		<updated>2024-04-16T05:44:28Z</updated>

		<summary type="html">&lt;p&gt;CSV import&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;[[File:Nephroma2.jpg|Nephroma2|thumb]] &amp;#039;&amp;#039;&amp;#039;Nephroma&amp;#039;&amp;#039;&amp;#039; is a term that can refer to different concepts depending on the context in which it is used. In the field of [[medicine]], it typically refers to a type of [[kidney tumor]], while in the realm of [[biology]], it pertains to a genus of [[lichens]]. This article will focus on the medical aspect of nephroma, specifically relating to its implications as a kidney tumor.&lt;br /&gt;
&lt;br /&gt;
==Overview==&lt;br /&gt;
Nephroma in the medical context, often termed as &amp;#039;&amp;#039;renal nephroma&amp;#039;&amp;#039; or &amp;#039;&amp;#039;kidney nephroma&amp;#039;&amp;#039;, is a rare, usually benign tumor that originates from the [[kidney]]&amp;#039;s tissues. Despite its benign nature, careful diagnosis and management are crucial due to the potential for misdiagnosis as more malignant forms of [[kidney cancer]].&lt;br /&gt;
&lt;br /&gt;
==Classification==&lt;br /&gt;
Kidney tumors are classified based on their histological appearance, origin, and potential for malignancy. Nephroma can be categorized into different types based on these criteria, including:&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Mesoblastic Nephroma&amp;#039;&amp;#039;&amp;#039;: This type is most commonly found in infants and is generally benign.&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;Adult Nephroma&amp;#039;&amp;#039;&amp;#039;: Rare in adults, these tumors can sometimes mimic more aggressive forms of kidney cancer and require thorough evaluation.&lt;br /&gt;
&lt;br /&gt;
==Symptoms==&lt;br /&gt;
The symptoms of nephroma can vary widely and may include:&lt;br /&gt;
* [[Hematuria]] (blood in the urine)&lt;br /&gt;
* Abdominal mass&lt;br /&gt;
* Pain in the side or lower back&lt;br /&gt;
* Fever&lt;br /&gt;
* Hypertension (high blood pressure)&lt;br /&gt;
&lt;br /&gt;
It&amp;#039;s important to note that these symptoms can also be associated with a variety of other kidney conditions, making accurate diagnosis essential.&lt;br /&gt;
&lt;br /&gt;
==Diagnosis==&lt;br /&gt;
Diagnosis of nephroma involves a combination of clinical evaluation and imaging studies. Techniques such as [[ultrasound]], [[computed tomography (CT) scan]], and [[magnetic resonance imaging (MRI)]] are commonly used to visualize the tumor. In some cases, a biopsy may be necessary to confirm the diagnosis and rule out malignancy.&lt;br /&gt;
&lt;br /&gt;
==Treatment==&lt;br /&gt;
The treatment for nephroma typically involves surgical removal of the tumor. In cases where the tumor is benign and poses no immediate health risk, careful monitoring may be recommended instead. The choice of treatment depends on several factors, including the size and location of the tumor, the patient&amp;#039;s overall health, and the potential for the tumor to become malignant.&lt;br /&gt;
&lt;br /&gt;
==Prognosis==&lt;br /&gt;
The prognosis for individuals with nephroma is generally good, especially for those with benign tumors that have been completely removed. Regular follow-up is important to monitor for any signs of recurrence or complications.&lt;br /&gt;
&lt;br /&gt;
==Conclusion==&lt;br /&gt;
Nephroma, while rare, represents an important diagnostic consideration in patients presenting with kidney-related symptoms. Due to its potential overlap with more aggressive kidney cancers, a thorough and careful diagnostic process is essential to ensure appropriate management and treatment.&lt;br /&gt;
&lt;br /&gt;
[[Category:Kidney diseases]]&lt;br /&gt;
[[Category:Tumors]]&lt;br /&gt;
&lt;br /&gt;
{{medicine-stub}}&lt;/div&gt;</summary>
		<author><name>Prab</name></author>
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