scholarly journals Modification of Diagnostic Criteria in Takotsubo Syndrome

2018 ◽  
Vol 86 (2) ◽  
pp. 79-81
Author(s):  
Yoshihiro J Akashi
Author(s):  
S.V. Kakorin ◽  
A. R. Ovezova ◽  
E. Yu. Rovda ◽  
P. Yu. Lopotovsky ◽  
N. B. Pavlova

ESC CardioMed ◽  
2018 ◽  
pp. 1278-1280
Author(s):  
Abhiram Prasad

Takotsubo syndrome (TTS) is also commonly known as apical ballooning syndrome and stress cardiomyopathy. The incidence of TTS has consistently been estimated to be close to 2% of all patients presenting with an initial diagnosis of an acute coronary syndrome, and perhaps as high as about 5% of women. TTS is a diagnosis of exclusion and in the absence of a diagnostic test, there is the need for diagnostic criteria. The Mayo Clinic diagnostic criteria are the most widely cited. The Heart Failure Association of the European Society of Cardiology published the most recent criteria in 2015.


2018 ◽  
Vol 39 (22) ◽  
pp. 2032-2046 ◽  
Author(s):  
Jelena-Rima Ghadri ◽  
Ilan Shor Wittstein ◽  
Abhiram Prasad ◽  
Scott Sharkey ◽  
Keigo Dote ◽  
...  

2014 ◽  
Vol 176 (1) ◽  
pp. 274-276 ◽  
Author(s):  
Björn Redfors ◽  
Yangzhen Shao ◽  
Alexander R. Lyon ◽  
Elmir Omerovic

ESC CardioMed ◽  
2018 ◽  
pp. 1278-1280
Author(s):  
Abhiram Prasad

Takotsubo syndrome (TTS) is also commonly known as apical ballooning syndrome and stress cardiomyopathy. The incidence of TTS has consistently been estimated to be close to 2% of all patients presenting with an initial diagnosis of an acute coronary syndrome, and perhaps as high as about 5% of women. TTS is a diagnosis of exclusion and in the absence of a diagnostic test, there is the need for diagnostic criteria. The Mayo Clinic diagnostic criteria are the most widely cited. The Heart Failure Association of the European Society of Cardiology published criteria in 2015. An update to this chapter includes the most recent criteria from 2018.


2018 ◽  
Vol 258 ◽  
pp. 29 ◽  
Author(s):  
Francesco Santoro ◽  
Thomas Stiermaier ◽  
Nicola Tarantino ◽  
Francesca Guastafierro ◽  
Tobias Graf ◽  
...  

Author(s):  
W.T. Gunning ◽  
G.D. Haselhuhn ◽  
E.R. Phillips ◽  
S.H. Selman

Within the last few years, adrenal cortical tumors with features concordant with the diagnostic criteria attributed to oncocytomas have been reported. To date, only nine reported cases exist in the literature. This report is the tenth case presentation of a presumptively benign neoplasm of the adrenal gland with a rare differentiation. Oncocytomas are well recognized benign tumors of the thyroid, parathyroid, and salivary glands and of the kidney. Other organs also give rise to these types of tumors, however with less frequency than the former sites. The characteristics generally used to classify a tumor as an oncocytoma include the following criteria: the tumor is 1) usually a solitary circumscribed mass with no gross nor microscopic evidence of metastasis (no tissue nor vascular invasion), 2) fairly bland in terms of mitotic activity and nuclear morphology, and 3) composed of large eosinophillic cells in which the cytoplasm is packed full of mitochondria (Figure 1).


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