Sickle cell trait: a cause of abdominal pain and pulmonary embolism
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. Ho...
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Formato: | Artículo revista |
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Universidad Nacional Cba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología
2020
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Acceso en línea: | https://revistas.unc.edu.ar/index.php/med/article/view/25077 |
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Universidad Nacional de Córdoba |
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Revistas de la UNC |
language |
Inglés |
format |
Artículo revista |
topic |
rasgo drepanocítico infarto del bazo embolia pulmonar inhibidor de coagulación del lupus. sickle cell trait splenic infarction pulmonary embolism lupus coagulation inhibitor. traço falciforme infarto do baço embolia pulmonar inibidor de coagulação do lúpus. |
spellingShingle |
rasgo drepanocítico infarto del bazo embolia pulmonar inhibidor de coagulación del lupus. sickle cell trait splenic infarction pulmonary embolism lupus coagulation inhibitor. traço falciforme infarto do baço embolia pulmonar inibidor de coagulação do lúpus. Saad, Emanuel José Tarditi Barra, Ayelén Monzoni, Gabriela Villegas, Carolina Tabares, Aldo Hugo Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
topic_facet |
rasgo drepanocítico infarto del bazo embolia pulmonar inhibidor de coagulación del lupus. sickle cell trait splenic infarction pulmonary embolism lupus coagulation inhibitor. traço falciforme infarto do baço embolia pulmonar inibidor de coagulação do lúpus. |
author |
Saad, Emanuel José Tarditi Barra, Ayelén Monzoni, Gabriela Villegas, Carolina Tabares, Aldo Hugo |
author_facet |
Saad, Emanuel José Tarditi Barra, Ayelén Monzoni, Gabriela Villegas, Carolina Tabares, Aldo Hugo |
author_sort |
Saad, Emanuel José |
title |
Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
title_short |
Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
title_full |
Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
title_fullStr |
Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
title_full_unstemmed |
Sickle cell trait: a cause of abdominal pain and pulmonary embolism |
title_sort |
sickle cell trait: a cause of abdominal pain and pulmonary embolism |
description |
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. |
publisher |
Universidad Nacional Cba. Facultad de Ciencias Médicas. Secretaria de Ciencia y Tecnología |
publishDate |
2020 |
url |
https://revistas.unc.edu.ar/index.php/med/article/view/25077 |
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