scholarly journals Sudden Cardiac Arrest - A Rare Presentation of Subarachnoid Hemorrhage

Author(s):  
M.T.T. Awad ◽  
S. Ghazaleh ◽  
Y. Khader ◽  
Z. Nesheiwat ◽  
A. Elzanaty ◽  
...  
Author(s):  
Divya Salhan ◽  
Deepak Sapkota ◽  
Prakash Verma ◽  
Saroj Kandel ◽  
Omar Abdulfattah ◽  
...  

2016 ◽  
Vol 1 (2) ◽  
pp. 132-135 ◽  
Author(s):  
Joseph Zachariah ◽  
Jessica A. Stanich ◽  
Sherri A. Braksick ◽  
Eelco FM. Wijdicks ◽  
Ronna L. Campbell ◽  
...  

2011 ◽  
Vol 50 (17) ◽  
pp. 1859-1859
Author(s):  
Wataru Mitsuma ◽  
Masahiro Ito ◽  
Hiroaki Obata ◽  
Makoto Kodama

PEDIATRICS ◽  
2017 ◽  
Vol 140 (4) ◽  
pp. e20162485 ◽  
Author(s):  
Isa Ozyilmaz ◽  
Bedir Akyol ◽  
Yakup Ergul

2019 ◽  
Vol 3 (9) ◽  
pp. 1678-1681 ◽  
Author(s):  
Nicole K Zern ◽  
Keith D Eaton ◽  
Mara Y Roth

Abstract Adrenocortical carcinoma (ACC) is a rare malignancy that usually is detected as a result of symptoms of hormone excess or mass effect. We describe a rare presentation of ACC with primary aldosterone production leading to profound hypokalemia and cardiac arrest. The patient was previously asymptomatic with low-grade, untreated hypertension and no documented electrolyte abnormalities. She had sudden cardiac arrest, and potassium levels were undetectable. After successful resuscitation, imaging showed a 6-cm left adrenal mass highly suspicious for malignancy. Biochemical workup revealed aldosterone excess as well as cortisol excess, despite the absence of Cushingoid symptoms. Histopathological examination after surgical resection demonstrated high-grade ACC. This case illustrates that the workup of cardiac arrest as a result of electrolyte abnormalities should include evaluation for adrenal pathology.


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