Multimodality versus single modality multiparametric imaging of carotid atherosclerotic disease - time to change the approach to patient evaluation?

VASA ◽  
2016 ◽  
Vol 45 (6) ◽  
pp. 433-435 ◽  
Author(s):  
Sasan Partovi ◽  
Brian B. Ghoshhajra
2016 ◽  
Vol 15 (1) ◽  
pp. 5-9 ◽  
Author(s):  
Domenico Toraldo ◽  
Michele Benedetto ◽  
Luana Conte ◽  
Francesco Nuccio

2001 ◽  
Vol 59 (s78) ◽  
pp. 9-13 ◽  
Author(s):  
Jan T. Kielstein ◽  
Stefanie M. Bode-Boger ◽  
Jurgen C. Frolich ◽  
Hermann Haller ◽  
Rainer H. Boger

2021 ◽  
pp. 004947552110206
Author(s):  
Prasad Dange ◽  
Ankesh Gupta ◽  
Richa Juneja ◽  
Renu Saxena

Long-standing moderate to marked splenomegaly suggests several differential diagnoses, both haematological and infectious, particularly leishmaniasis and malaria in endemic areas. Non-infectious causes may be missed in these regions, especially if pitfalls of serological testing are not considered. Careful patient evaluation is necessary to arrive at the correct diagnosis. We report a case of a young male whose hereditary spherocytosis was initially missed because of RK-39 positivity, splenomegaly and the fact that he hailed from an endemic region.


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