scholarly journals A case of pulmonary thromboembolism and splenic infarction in mycoplasma pneumonia

2021 ◽  
Vol 9 (1) ◽  
pp. 36
Author(s):  
Eun Wook Kwon ◽  
Dong Won Lee
2020 ◽  
Vol 77 (4) ◽  
pp. 360-362
Author(s):  
Emanuel José Saad ◽  
Ayelén Tarditi Barra ◽  
Gabriela Monzoni ◽  
Carolina Villegas ◽  
Aldo Hugo Tabares

Introduction: Sickle cell trait (SCT) is a rare and underdiagnosed disorder in the Argentinian population. In this condition, individuals carry the mutation of the HbS gene in one of the two beta-globin genes. In general, SCT does not present with the typical manifestations of sickle cell anemia. However, under certain circumstances, some clinical characteristics of the disease may develop. Methods: We discussed the case of a 39-Year old man who presented with persistent abdominal pain of unknown origin after traveling to a high-altitude place. He underwent laparotomy without a definite diagnosis. After that, the patient developed signs of splenic infarction and pulmonary thromboembolism that were confirmed by computed tomography. Results: A sickling test was positive, and a hemoglobin electrophoresis revealed an abnormal fraction at the HbS level. In this context a diagnosis of SCT was made. Additional, tests revealed a strongly positive lupus anticoagulant. Conclusion: SCT presentation as abdominal pain and thromboembolic disease in adult patients after exposure to high altitudes is a rarely suspected diagnosis.


JAMA ◽  
1965 ◽  
Vol 194 (4) ◽  
pp. 336-338 ◽  
Author(s):  
R. D. Sautter

2003 ◽  
Vol 48 (4) ◽  
pp. 361
Author(s):  
Jung Eun Cheon ◽  
Woo Sun Kim ◽  
In One Kim ◽  
Young Yull Koh ◽  
Hoan Jong Lee ◽  
...  

1999 ◽  
Vol 41 (2) ◽  
pp. 407 ◽  
Author(s):  
Soo Hyeon Lee ◽  
Joung Sook Kim ◽  
Jung Hee Yoon ◽  
Gham Hur ◽  
Chang Gun Kim
Keyword(s):  

2019 ◽  
Vol 81 (3) ◽  
pp. 170-174 ◽  
Author(s):  
Taketoshi IDE ◽  
Maiko OHNO ◽  
Takamichi ITO ◽  
Karin TSUKAMOTO ◽  
Anna HIRANO ◽  
...  

1990 ◽  
Vol 1 (1) ◽  
pp. 36-40
Author(s):  
Hiroshi HASEGAWA

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