scholarly journals A RARE CASE OF VASCULAR ANOMALY OF THE VERTEBROBASILAR SYSTEM IN A PATIENT WITH MIXED TYPE VERTIGO

2018 ◽  
Vol 8 (3) ◽  
pp. 49-54
Keyword(s):  
Rare Case ◽  
Mixed Type ◽  
Vascular Anomaly ◽  
Vertebrobasilar System

scholarly journals Intranodal capillary-cavernous hemangioma: Report of a very rare case

2019 ◽  
Vol 7 ◽  
pp. 2050313X1984671
Author(s):  
Jérôme Tessieras ◽  
Jinane Chenaye ◽  
Christophe Senechaud ◽  
Yara Banz
Keyword(s):  
Magnetic Resonance Imaging ◽  
Endothelial Cells ◽  
Differential Diagnosis ◽  
Magnetic Resonance ◽  
Cavernous Hemangioma ◽  
Rare Case ◽  
Mixed Type ◽  
Vascular Anomaly ◽  
Vascular Lesion ◽  
Resonance Imaging

Mixed type capillary-cavernous hemangioma is a rare vascular anomaly, with an intranodal localization being extremely rare. Its finding is often accidental but may be clinically symptomatic. The diagnosis relies on histopathology, showing a proliferation of capillaries and cavernous vessels filled with erythrocytes and lined by endothelial cells. Magnetic resonance imaging with enhanced and T2 STIR sequences is the most efficient imaging for diagnosing this type of hemangioma. Rarely, malignancy or another vascular lesion can be evoked as a differential diagnosis of mixed hemangioma. Treatment in this localization is often surgical, even if other possibilities exist for other areas. In this article, we describe a very rare case of intranodal capillary-cavernous hemangioma.

A rare case of a rapidly expanding high flow vascular anomaly

Pathology ◽  
2019 ◽  
Vol 51 ◽  
pp. S104-S105
Author(s):  
Francis H.X. Yap ◽  
Susan Adams ◽  
Christine Loo
Keyword(s):  
Rare Case ◽  
Vascular Anomaly ◽  
High Flow

A rare case of mixed type liposarcoma of breast arising in malignant phyllodes tumor

2019 ◽  
Vol 26 (2) ◽  
pp. 271-273 ◽  
Author(s):  
Jae‐Myung Kim ◽  
Eun Jung Jung ◽  
Ju‐Yeon Kim ◽  
Han Shin Lee ◽  
Hyo Jung An ◽  
...  
Keyword(s):  
Rare Case ◽  
Mixed Type ◽  
Phyllodes Tumor ◽  
Malignant Phyllodes Tumor

scholarly journals Incidental Finding of Complete Bilateral Persistent Sciatic Arteries

2021 ◽  
Vol 8 (1) ◽  
pp. 2
Author(s):  
Sofia M. Ramos ◽  
Reinhardt G. Dreyer ◽  
Thandi E. Buthelezi
Keyword(s):  
Computed Tomography ◽  
Lower Limb ◽  
Rare Case ◽  
Gunshot Wound ◽  
Incidental Finding ◽  
Treatment Options ◽  
Vascular Anomaly ◽  
Young Female ◽  
Imaging Findings ◽  
Accurate Reporting

Persistence of bilateral sciatic arteries (PSA) is a rare congenital vascular anomaly. We report an exceptionally rare case of complete bilateral persistent sciatic arteries, diagnosed incidentally on computed tomography angiography (CTA) in a young female patient who sustained a gunshot wound to the lower limb. The embryology, variants, clinical and imaging findings, potential complications, and treatment options are discussed. PSAs, found incidentally, are unlikely to have clinical significance, however, the unusual anatomy and higher incidence of future complications requires accurate reporting of such variants.

A Rare Case of Ischemic Colitis Due to an Inferior Mesenteric Vascular Anomaly Leading to Steal Phenomenon

2017 ◽  
Vol 112 ◽  
pp. S1067-S1068
Author(s):  
Dimitri Gitelmaker ◽  
Robert J. Bierwirth ◽  
Ethan Prince ◽  
Alan Epstein ◽  
Benjamin Young
Keyword(s):  
Ischemic Colitis ◽  
Rare Case ◽  
Vascular Anomaly ◽  
Steal Phenomenon

A RARE CASE OF CEREBRO-VASCULAR ANOMALY

2005 ◽  
Vol 26 (S 1) ◽  
Author(s):  
R Radulescu-Botica ◽  
D Pelinescu-Onciul ◽  
M Bari
Keyword(s):  
Rare Case ◽  
Vascular Anomaly

scholarly journals ​Venous anomalies in renal transplantation: an accessory left-sided IVC in a live kidney donor

2019 ◽  
Vol 12 (12) ◽  
pp. e232695
Author(s):  
Jack Whooley ◽  
Atakelet Ferede ◽  
Gordon Smyth ◽  
Dilly Little
Keyword(s):  
Rare Case ◽  
Inferior Vena ◽  
Vena Cava ◽  
Vascular Anomaly ◽  
Iliac Vein ◽  
Common Iliac Vein ◽  
Kidney Donor ◽  
Left Common Iliac Vein ◽  
Live Kidney Donor ◽  
The Right

Duplication of the inferior vena cava (IVC) resulting in an accessory left-sided IVC is a relatively rare vascular anomaly with a reported prevalence of 0.7%. Radiologically, a duplicated left-sided IVC is usually seen as a continuation of the left common iliac vein, crossing anterior to the aorta at the level of the renal vein to join the right-sided IVC. We present a rare case in which an accessory left-sided IVC was discovered intraoperatively, in a 47-year-old living donor, posing significant intraoperative challenges regarding extraction and subsequent transplantation.

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