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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Autores principales: Saad, Emanuel José, Tarditi Barra, Ayelén, Monzoni, Gabriela, Villegas, Carolina, Tabares, Aldo Hugo
Formato: Artículo revista
Lenguaje:Inglés
Publicado: 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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id I10-R10article-25077
record_format ojs
institution Universidad Nacional de Córdoba
institution_str I-10
repository_str R-10
container_title_str 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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