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July 2015 Issue

 




Other Radiology articles from the Neuroradiology section Neuroradiology

Cystoid angiocentric glioma: A case report and literature review by Sainan Cheng et al.

Published: 2015 Jul
Issue: 9(7) :: Pages: 1-9


Free full text article: Cystoid angiocentric glioma:  A case report and literature review

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Abstract: Angiocentric glioma is a rare subtype of neuroepithelial tumor that is associated with a history of epilepsy. We report a case of cystoid angiocentric glioma associated with an area of calcification. This 25 year old male patient presented with tonic clonic spasm. He underwent craniotomy with complete resection of the lesion. Pathologic specimen showed monomorphous bipolar cells with angiocentric growth pattern.


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Computed Tomography, Magnetic Resonance Imaging, Microscopic pathology, Table





Other Radiology articles from the OB/GYN section OB/GYN

Hemorrhagic heterotopic pregnancy in a setting of prior tubal ligation and re-anastomosis by Jason Esterle et al.

Published: 2015 Jul
Issue: 9(7) :: Pages: 38-46


Free full text article: Hemorrhagic heterotopic pregnancy in a setting of prior tubal ligation and re-anastomosis

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Abstract: Heterotopic pregnancy is the occurrence of simultaneous intrauterine and extrauterine pregnancies. Heterotopic pregnancy most commonly occurs during the first trimester of pregnancy in women who have significant risk factors including assisted reproductive therapy, prior ectopic pregnancy, and prior pelvic surgery or pelvic inflammatory disease. Although rare, heterotopic pregnancy must be recognized using ultrasound so as to provide appropriate treatment to the extrauterine pregnancy with the goal of preserving the intrauterine pregnancy. The case presented describes a patient with a pathologically proven (figure 8A and 8B), surgically treated 1st trimester heterotopic pregnancy.


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Ultrasound, Other, Microscopic pathology, Table





Other Radiology articles from the Cardiac Imaging section Cardiac Imaging

Cardiovascular magnetic resonance and computed tomography in the evaluation of aneurysmal coronary-cameral fistula by Efstathios E Detorakis et al.

Published: 2015 Jul
Issue: 9(7) :: Pages: 10-21


Free full text article: Cardiovascular magnetic resonance and  computed tomography in the evaluation  of aneurysmal coronary-cameral fistula

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Abstract: Coronary artery fistulas represent abnormal communications between a coronary artery and a major vessel like venae cavae, pulmonary arteries or veins, the coronary sinus, or a cardiac chamber. The latter is called coronary cameral fistula is a rare condition and is most of the times congenital but can be also post traumatic or post surgical, especially after cardiovascular interventional procedures. Most patients are asymptomatic and coronary-cameral fistulae are discovered incidentally during angiographic evaluation for coronary vascular disorders, while other patients have a clinical presentation ranging from angina pectoris to heart failure. In this article, we report a rare case of an aneurysmal right coronary cameral fistula draining into the left ventricle. Echocardiography usually represents the first diagnostic imaging approach, but often due to a poor acoustic window may not show the entire course of the fistula which is crucial for the final diagnosis. ECG-gated cardiovascular CT may play an important role in the evaluation of the origin, course, termination and morphology of the fistula, its relation to the adjacent anatomical structures as well as the morphology and contractility of the heart. Cardiac MRI instead plays an additional crucial role regarding not only the above mentioned factors but also in estimating the blood flow within the fistula, providing more detailed information about the cardiac function but also about myocardial wall viability.


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Ultrasound, Conventional Radiography, Computed Tomography, Magnetic Resonance Imaging, Angiography, Interventional, Table





Other Radiology articles from the Gastrointestinal Radiology section Gastrointestinal Radiology

Heterotaxy Polysplenia Syndrome In An Adult With Unique Vascular Anomalies: Case Report With Review Of Literature by Chittapuram Srinivasan Rameshbabu et al.

Published: 2015 Jul
Issue: 9(7) :: Pages: 22-37


Free full text article: Heterotaxy Polysplenia Syndrome In An Adult With Unique Vascular Anomalies:  Case Report With Review Of Literature

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Abstract: The pattern of anatomical organization of the thoraco-abdominal visceral and vascular structures which is not the expected normal arrangement, is called as situs ambiguous or heterotaxy syndrome. Patients with heterotaxy syndrome exhibit a wide spectrum of anatomical variations involving thoraco-abdominal structures. We present here an incidental finding of heterotaxy syndrome associated with unique vascular anomalies in a 35 year old male patient evaluated initially for nephrolithiasis by ultrasonography, and intravenous pyelography. Further evaluation by multidetector row computed tomography showed bilateral bilobed lungs with hyparterial bronchi, cardiac apex to the left, five branches from left-sided aortic arch with retroesophageal right subclavian artery, interrupted inferior vena cava with azygos continuation, left renal vein continuing as hemiazygos vein and replaced common hepatic artery arising from the superior mesenteric artery. Other vascular anomalies include right internal iliac vein joining the left common iliac vein and precaval course of the single main right renal artery. Anomalies involving abdominal organs include right-sided stomach, midline liver, multiple splenules (polysplenia) in right upper quadrant of abdomen, short truncated pancreas, intestinal malrotation, inversion of superior mesenteric vessels and a preduodenal portal vein. To the best of our knowledge this is the first report of association of left renal vein continuing as hemiazygos vein, precaval right renal artery and anomalous branching pattern of aortic arch with heterotaxy syndrome.


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Ultrasound, Computed Tomography, Table





Other Radiology articles from the Pediatric Radiology section Pediatric Radiology

Primary synovial sarcoma of the abdominal wall: a case report and literature review by Supika Kritsaneepaiboon et al.

Published: 2015 Jul
Issue: 9(7) :: Pages: 47-52


Free full text article: Primary synovial sarcoma of the abdominal wall:  a case report and literature review

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Abstract: Synovial sarcoma (SS) is the fourth most common type of soft tissue sarcoma, following malignant fibrous histiocytoma, liposarcoma, and rhabdomyosarcoma. It usually occurs in the extremities near the large joints of middle-aged patients. We describe a case of synovial sarcoma of the anterior abdominal wall (SSAW) in an adolescent girl and undertake a review of the literature.


Available image modalities: (click on modality to browse for other articles)
Ultrasound, Computed Tomography, Macroscopic pathology, Microscopic pathology, Table





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