Ostomy function after abdominoperineal resection—a clinical and patient evaluation

2012 ◽  
Vol 27 (10) ◽  
pp. 1267-1274 ◽  
Author(s):  
E. Angenete ◽  
A. Correa-Marinez ◽  
J. Heath ◽  
E. González ◽  
A. Wedin ◽  
...  
1998 ◽  
Vol 39 (6) ◽  
pp. 1203
Author(s):  
Jung Suk Lee ◽  
Byung Ran Park ◽  
Un Hyeon Moon ◽  
Dong Cheol Yang ◽  
Joo Hyeon Im ◽  
...  

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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