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	<title>Radiology Picture of the Day</title>
	<atom:link href="http://www.radpod.org/feed/" rel="self" type="application/rss+xml" />
	<link>http://www.radpod.org</link>
	<description>A new medical image daily, with a brief description</description>
	<pubDate>Tue, 13 May 2008 16:01:28 +0000</pubDate>
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	<language>en</language>
			<item>
		<title>Leptomeningeal Haemosiderosis</title>
		<link>http://www.radpod.org/2008/05/14/leptomeningeal-haemosiderosis/</link>
		<comments>http://www.radpod.org/2008/05/14/leptomeningeal-haemosiderosis/#comments</comments>
		<pubDate>Tue, 13 May 2008 16:01:28 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Brain]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1033</guid>
		<description><![CDATA[<a href='None'><img src="http://www.radpod.org/wp-content/uploads/2008/05/haemosiderosis-75x84.jpg" alt="" title="leptomeningeal haemosiderosis" width="75" height="84" class="alignnone size-thumbnail wp-image-1034" /></a>]]></description>
			<content:encoded><![CDATA[<p><img src="http://www.radpod.org/wp-content/uploads/2008/05/haemosiderosis.jpg" alt="" title="leptomeningeal haemosiderosis" width="501" height="565" class="alignnone size-medium wp-image-1034" /></a></p>
<p>This patient presented with bilateral sensorineural hearing loss and dizziness. The axial T2-weighted MR image above shows signal loss over the cerebellar folia, a characteristic finding in leptomeningeal (a.k.a. superficial) haemosiderosis.</p>
<p>Leptomeningeal haemosiderosis typically presents with hearing loss and vestibular dysfunction as the vestibulocochlear nerve is particularly sensitive to it. Presentation may be with other cranial neuropathies, or cerebellar dysfunction. The condition may also be asymptomatic. The aetiology is considered to be repeated subarachnoid haemorrhages, and a search for a source is indicated. This should include spinal MR. Amyloid angiopathy has been described as a cause.</p>
<p>Reference: Linna J, et al. Subarachnoid hemosiderosis and superficial cortical hemosiderosis in cerebral amyloid angiopathy. <em>AJNR</em> 2008;29:184-186</p>
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		<item>
		<title>Tuberculosis of the Spine</title>
		<link>http://www.radpod.org/2008/05/12/tuberculosis-of-the-spine/</link>
		<comments>http://www.radpod.org/2008/05/12/tuberculosis-of-the-spine/#comments</comments>
		<pubDate>Sun, 11 May 2008 16:01:09 +0000</pubDate>
		<dc:creator>Aadil Ahmed</dc:creator>
		
		<category><![CDATA[Spine]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1030</guid>
		<description><![CDATA[<a href='None'><img src="http://www.radpod.org/wp-content/uploads/2008/05/tb_spine1-75x114.jpg" alt="" title="tuberculosis of the spine" width="75" height="114" class="alignnone size-thumbnail wp-image-1032" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/05/tb_spine1.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/tb_spine1.jpg" alt="" title="tuberculosis of the spine" width="311" height="475" class="alignnone size-medium wp-image-1032" /></a><br />
Extradural and paraspinal mass in patient with tuberculous discitis with resultant destruction of the disc and extension into the adjacent vertebral bodies. Subligamentous spread of disease is typical and evident on this image. Due to the local destruction there is resultant gibbus deformity of the thoracic spine. There is also spinal stenosis at the level in question by the extradural cold abcess. Tuberculous spondylitis is also called Pott&#8217;s disease of the spine</p>
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		<item>
		<title>Sickle Cell Anaemia</title>
		<link>http://www.radpod.org/2008/05/09/sickle-cell-anaemia/</link>
		<comments>http://www.radpod.org/2008/05/09/sickle-cell-anaemia/#comments</comments>
		<pubDate>Thu, 08 May 2008 16:01:29 +0000</pubDate>
		<dc:creator>Dr Ian Bickle</dc:creator>
		
		<category><![CDATA[Gastrointestinal]]></category>

		<category><![CDATA[Musculoskeletal]]></category>

		<category><![CDATA[Paediatrics]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1028</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/05/axr-sicklecellsplenomegalyavn.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/axr-sicklecellsplenomegalyavn-75x86.jpg" alt="" title="sickle cell anaemia with splenomegaly and femoral avascular necrosis" width="75" height="86" class="alignnone size-thumbnail wp-image-1029" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/05/axr-sicklecellsplenomegalyavn.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/axr-sicklecellsplenomegalyavn-520x600.jpg" alt="" title="sickle cell anaemia with splenomegaly and femoral avascular necrosis" width="520" height="600" class="alignnone size-medium wp-image-1029" /></a><br />
Sickle cell anaemia is an autosomal recessive genetic disease leading to production of a defective form of haemoglobin, haemoglobin S (HbS) causing sickle shaped erythrocytes. The major consequence of these sickled erthrocytes is that they much less deformable causing obstruction in the microcirculation.</p>
<p>Manifestations in the spleen include splenomegaly in childhood, with splenic infarction and autosplenectomy in adults.</p>
<p>Skeletal manifestations include avascular necrosis of the femoral head and H -shaped vertebrae.</p>
<p>This AXR shows massive splenomegaly and bilateral femoral head AVN.</p>
<p>Reference: <a href="http://www.emedicine.com/EMERG/topic26.htm" onclick="javascript:pageTracker._trackPageview('/outbound/article/www.emedicine.com');">eMedicine</a></p>
]]></content:encoded>
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		<item>
		<title>Cervical Incompetence</title>
		<link>http://www.radpod.org/2008/05/08/cervical-incompetence-2/</link>
		<comments>http://www.radpod.org/2008/05/08/cervical-incompetence-2/#comments</comments>
		<pubDate>Wed, 07 May 2008 16:01:35 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Obstetrics]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1027</guid>
		<description><![CDATA[<img id="image24" width=75 alt="cervical incompetence" src="http://radpod.org/wp-content/uploads/2006/11/cervical_incompetence.thumbnail.jpg" />]]></description>
			<content:encoded><![CDATA[<p><img id="image24" width=720 alt="cervical incompetence" src="http://radpod.org/wp-content/uploads/2006/11/cervical_incompetence.jpg" /></p>
<p>A sagittal transvaginal ultrasound image of the cervix at 21 weeks gestation shows funnelling of the proximal cervix, and reduction of the functional length to 10mm.<br />
Cervical incompetence is variably defined, however a cervical length of <25mm is often used. The risk of preterm delivery is inversely proportional to cervical length - 18% for <25mm and 25% for <20mm. The presence of funnelling is important. Greater than 50% funnelling before 25 weeks is associated with 80% risk of preterm delivery.</p>
<p>Patients at high risk for preterm delivery include: uterine anomalies; previous cervical trauma or surgery; history of recurrent spontaneous or therapeutic abortion; history of preterm (<32 weeks) birth. Transvaginal sonography is most commonly used to assess the cervix, however translabial and transperineal techniques have been used.</p>
<p>Management is controversial, with conflicting results, particularly regarding the efficacy of cerclage. Bed-rest, tocolysis, cerclage, and administration of steroids to accelerate foetal lung maturity are all treatment options to be considered. A recent metaanalysis suggests that cerclage is effective in reducing preterm births by 26% in singleton pregnancies (3).</p>
<p>References:<br />
1. Callen PW <i>Ultrasonography in Obstetrics and Gynecology</i>. 4th edition. WB Saunders, 2000<br />
2. Woodward PJ <i>Pocket Radiologist Obstetrics Top 100 Diagnoses</i> 1st edition. Amirsys / WB Saunders, 2003<br />
3. Berghella V, et al <i>Cerclage for short cervix on ultrasonography: meta-analysis of trials using individual patient-level data</i>. Obstetrics &#038; Gynecology. 106(1):181-9, 2005 Jul.</p>
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		</item>
		<item>
		<title>Retained Surgical Sponge</title>
		<link>http://www.radpod.org/2008/05/07/retained-surgical-sponge/</link>
		<comments>http://www.radpod.org/2008/05/07/retained-surgical-sponge/#comments</comments>
		<pubDate>Tue, 06 May 2008 16:01:16 +0000</pubDate>
		<dc:creator>jhamilton</dc:creator>
		
		<category><![CDATA[Gastrointestinal]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1025</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/05/retained_surgical_sponge.png'><img src="http://www.radpod.org/wp-content/uploads/2008/05/retained_surgical_sponge-75x98.png" alt="sagittal CT reformat of retained surgical sponge after 10 years in situ" title="retained_surgical_sponge" width="75" height="98" class="alignnone size-thumbnail wp-image-1026" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/05/retained_surgical_sponge.png'><img src="http://www.radpod.org/wp-content/uploads/2008/05/retained_surgical_sponge-459x600.png" alt="sagittal CT reformat of retained surgical sponge after 10 years in situ" title="retained_surgical_sponge" width="459" height="600" class="alignnone size-medium wp-image-1026" /></a></p>
<p>Gossypiboma is the name given to a retained surgical sponge, pad, or towel (gossypium (Latin), cotton; + plboma (Swahili), place of concealment).  Retained foreign bodies can cause either an acute inflammatory response or a chronic fibrinous response and so there is a very wide variation in the time course in which they are discovered, as evidence in a diverse array of case reports in the surgical and radiologic literature.  The sponge in the above picture was found over a decade after an exploratory laparotomy for trauma as an incidental finding on a study performed for an unrelated reason.</p>
<p>Policies and procedures such as thorough surgical instrument counts and intraoperative x-rays are designed to prevent this complication, however retained surgical instruments continue to be occur at a rate estimated to be around one in 1500 laparotomies.  It has been proposed that routine intraoperative x-rays are cost effective and should be performed for high-risk procedures despite correct instrument counts.</p>
<p>Surgical sponges are easily identified by the use of barium-impregnated threads woven into one side of the cloth.</p>
<p>Reference: N Engl J Med. 2003;348(3):228, 229-235</p>
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		</item>
		<item>
		<title>Chondrosarcoma of Petrous Apex</title>
		<link>http://www.radpod.org/2008/05/06/chondrosarcoma-of-petrous-apex/</link>
		<comments>http://www.radpod.org/2008/05/06/chondrosarcoma-of-petrous-apex/#comments</comments>
		<pubDate>Mon, 05 May 2008 16:01:13 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Head &amp; Neck]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1023</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/05/chondrosarcoma_t2_ax.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/chondrosarcoma_t2_ax-75x87.jpg" alt="" title="chondrosarcoma axial T2W MR" width="75" height="87" class="alignnone size-thumbnail wp-image-1024" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/05/chondrosarcoma_t2_ax.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/chondrosarcoma_t2_ax.jpg" alt="" title="chondrosarcoma axial T2W MR" width="515" height="600" class="alignnone size-medium wp-image-1024" /></a></p>
<p>This axial T2-weighted MR image shows a high signal lesion in the petrous apex region, also involving the clivus. The lesion is expansile and there is evidence of bone destruction. Histopathology demonstrated chondrosarcoma.</p>
<p>Chondrosarcomas of the skull base are typically off-midline, destructive lesions with high T2 signal and strong but heterogeneous contrast-enhancement. Approximately 50% demonstrate chondroid matrix calcification (best seen on CT).</p>
<p>Skull base chondrosarcoma has a better prognosis than skull base chordoma, with an 80% 5-year progression-free survival after resection and radiotherapy.</p>
<p>References:<br />
1. Osborn A. <em>Diagnostic Neuroradiology</em> Mosby 1994<br />
2. Cho YH, et al. Chordomas and chondrosarcomas of the skull base: comparative analysis of clinical results in 30 patients. <em>Neurosurg Rev</em> 2008;31(1):35-43</p>
]]></content:encoded>
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		</item>
		<item>
		<title>Venous Vascular Malformation</title>
		<link>http://www.radpod.org/2008/05/05/venous-vascular-malformation-2/</link>
		<comments>http://www.radpod.org/2008/05/05/venous-vascular-malformation-2/#comments</comments>
		<pubDate>Sun, 04 May 2008 16:01:36 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Head &amp; Neck]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1022</guid>
		<description><![CDATA[<img id="image23" width=75 alt="venous vascular malformation" src="http://radpod.org/wp-content/uploads/2006/11/vascular_malformation.thumbnail.jpg" />]]></description>
			<content:encoded><![CDATA[<p><img id="image23" alt="venous vascular malformation" src="http://radpod.org/wp-content/uploads/2006/11/vascular_malformation.jpg" /></p>
<p>Coronal T2W MRI of the head and neck of a 20 year-old male. There are areas of high signal with a trans-spatial distribution: base of tongue; the tonsillar region; the masticator space; the subcutaneous tissues of the neck; and the deep neck spaces including the larynx and upper trachea. This appearance is characteristic of vascular malformation. There are areas of low signal within some of the vascular spaces, consistent with phleboliths.</p>
<p>Vascular malformations are classified according to Mulliken &#038; Glowacki, 1982. They may be low-flow (venous, capillary, lymphatic, or mixed) or high-flow (arteriovenous) malformations. Vascular malformations are non-proliferative congenital abnormalities. They should be differentiated from capillary haemangioma of infancy, a common proliferative lesion. Vascular malformations (especially mixed type) are associated with Klippel-Trenaunay, Osler-Weber-Rendu, Maffucci, blue-rubber-bleb naevus, and other syndromes. Frequently there is associated tissue hypertrophy, although atrophy may also occur. Lesions are typically trans-spatial, involving subcutaneous, muscle, joint, bone and organ compartments.</p>
<p>Clinical presentation of venous malformation may be with cosmetic deformity, pain, haemorrhage, thrombosis, loss of function, or compression of vital structures. Management of these complex lesions is best undertaken in a multidisiplinary team environment, in specialised vascular birthmark clinics. Treatment may be with surgical excision or sclerotherapy. Surgical excision is often complicated by recurrence, as complete excision is rarely possible. Sclerotherapy with ethanol or foamed surfactants has been shown to be efficacious in reducing the symptoms and complications, and the complication rate is low. Complications of sclerotherapy include skin ulceration, sclerosant embolisation and nerve palsy.</p>
<p>References:<br />
1. Mulliken JB &#038; Glowacki J. Hemangiomas and Vascular Malformations in Infants and Children: A Classification Based on Endothelial Characteristics. <i>Plast. Reconst. Surg.</i> 1982; 69(3):412-420<br />
2. Burrows PE. Percutaneous Treatment of Low Flow Vascular Malformations. <i>J Vasc Interv Radiol.</i> 2004; 15:431-445</p>
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		</item>
		<item>
		<title>Neuropathic Osteoarthropathy</title>
		<link>http://www.radpod.org/2008/05/02/neuropathic-osteoarthropathy/</link>
		<comments>http://www.radpod.org/2008/05/02/neuropathic-osteoarthropathy/#comments</comments>
		<pubDate>Thu, 01 May 2008 16:01:18 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Musculoskeletal]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1020</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/05/charcot_lat.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/charcot_lat-75x54.jpg" alt="" title="neuropathic osteoarthropathy" width="75" height="54" class="alignnone size-thumbnail wp-image-1021" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/05/charcot_lat.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/05/charcot_lat.jpg" alt="" title="neuropathic osteoarthropathy" width="718" height="521" class="alignnone size-medium wp-image-1021" /></a></p>
<p>This lateral radiograph of the foot demonstrates the typical findings of neuropathic osteoarthropathy. The most common cause is diabetes mellitus. Findings include bone sclerosis, new bone formation, articular destruction and deformity, loose bodies, and subluxations / dislocations. Soft tissue swelling and joint effusions are also a feature.</p>
<p>Reference: Dahnert W. <em>Radiology Review Manual</em> 5th ed. Lippincott, Williams &#038; Wilkins 2003 </p>
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		</item>
		<item>
		<title>Perineural Metastasis</title>
		<link>http://www.radpod.org/2008/05/01/perineural-metastasis/</link>
		<comments>http://www.radpod.org/2008/05/01/perineural-metastasis/#comments</comments>
		<pubDate>Wed, 30 Apr 2008 16:01:15 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Head &amp; Neck]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1017</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/04/facial_nerve_enh.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/04/facial_nerve_enh-75x84.jpg" alt="" title="perineural spread of adenoid cystic carcinoma" width="75" height="84" class="alignnone size-thumbnail wp-image-1018" /></a>
]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/04/facial_nerve_enh_annot.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/04/facial_nerve_enh-531x600.jpg" alt="" title="perineural spread of adenoid cystic carcinoma" width="531" height="600" class="alignnone size-medium wp-image-1018" /></a><br />
This patient had known left parotid adenoid cystic carcinoma. The axial T1-weighted fat-saturated gadolinium-enhanced MR image shows enlargement and enhancement of the left facial nerve at the stylomastoid foramen (click image for an annotated version).<br />
Adenoid cystic carcinoma is notorious for its ability to metastasise by perineural spread.<br />
Facial nerve perineural enhancement may be a normal finding within the bony facial canal. Enhancement outside of the canal (below the skull base, within the internal auditory meatus, or in the cerebellopontine angle cistern) is always pathological. Other signs of perineural invasion are nerve thickening and widening of the bony canal. MR is more accurate when detecting perineural invasion than CT.<br />
References:<br />
1. Gebarski SS, Telian SA, Niparko JK. Enhancement along the normal facial nerve in the facial canal: MR imaging and anatomic correlation. <em>Radiology</em> 1992;183:391-394<br />
2. Hanna E, et al. The sensitivity and specificity of high-resolution imaging in evaluating perineural spread of adenoid cystic carcinoma to the skull base. <em>Arch Otolaryngol Head Neck Surg</em> 2007;133(6):541-5</p>
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		</item>
		<item>
		<title>Median Artery of the Corpus Callosum</title>
		<link>http://www.radpod.org/2008/04/30/median-artery-of-the-corpus-callosum/</link>
		<comments>http://www.radpod.org/2008/04/30/median-artery-of-the-corpus-callosum/#comments</comments>
		<pubDate>Tue, 29 Apr 2008 16:01:45 +0000</pubDate>
		<dc:creator>Dr Laughlin Dawes</dc:creator>
		
		<category><![CDATA[Brain]]></category>

		<guid isPermaLink="false">http://www.radpod.org/?p=1015</guid>
		<description><![CDATA[<a href='http://www.radpod.org/wp-content/uploads/2008/04/aca_anomaly1.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/04/aca_anomaly1-75x79.jpg" alt="median artery of the corpus callosum" title="aca_anomaly1" width="75" height="79" class="alignnone size-thumbnail wp-image-1016" /></a>]]></description>
			<content:encoded><![CDATA[<p><a href='http://www.radpod.org/wp-content/uploads/2008/04/aca_anomaly1.jpg'><img src="http://www.radpod.org/wp-content/uploads/2008/04/aca_anomaly1.jpg" alt="median artery of the corpus callosum" title="aca_anomaly1" width="522" height="555" class="alignnone size-medium wp-image-1016" /></a><br />
This time-of-flight MR angiogram shows 3 A2 segments of the anterior cerebral arteries. The central (anomalous) one arises from the anterior communicating artery, and is known as a median artery of the corpus callosum. This anomaly occurs in 3% of the population. As with other ACA anomalies, there is an increased incidence of cerebral aneurysm.<br />
Other ACA anomalies include unilateral hypoplastic A1 segment (6%), azygous (unpaired) A2 (2%), fenestrations (1%) and asymmetric A2 segments (bihemispheric A2). The incidence of ACA aneurysms in patients with unilateral hypoplastic A1 is around 14%, and is thought to be due to altered haemodynamic stresses at the A1/A2/ACOM junction.</p>
<p>Reference: Uchino A, et al. Anterior cerebral artery variations detected by MR angiography. <em>Neuroradiology</em> 2006;48:647-652</p>
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