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
2019 ◽  
Vol 7 ◽  
pp. 2050313X1984671
Author(s):  
Jérôme Tessieras ◽  
Jinane Chenaye ◽  
Christophe Senechaud ◽  
Yara Banz

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.


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

2019 ◽  
Vol 26 (2) ◽  
pp. 271-273 ◽  
Author(s):  
Jae‐Myung Kim ◽  
Eun Jung Jung ◽  
Ju‐Yeon Kim ◽  
Han Shin Lee ◽  
Hyo Jung An ◽  
...  

2021 ◽  
Vol 8 (1) ◽  
pp. 2
Author(s):  
Sofia M. Ramos ◽  
Reinhardt G. Dreyer ◽  
Thandi E. Buthelezi

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.


2017 ◽  
Vol 112 ◽  
pp. S1067-S1068
Author(s):  
Dimitri Gitelmaker ◽  
Robert J. Bierwirth ◽  
Ethan Prince ◽  
Alan Epstein ◽  
Benjamin Young

Author(s):  
R Radulescu-Botica ◽  
D Pelinescu-Onciul ◽  
M Bari
Keyword(s):  

2019 ◽  
Vol 12 (12) ◽  
pp. e232695
Author(s):  
Jack Whooley ◽  
Atakelet Ferede ◽  
Gordon Smyth ◽  
Dilly Little

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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