Case of Situs Inversus Totalis-A report

Published On 2019-06-17 12:30 GMT   |   Update On 2019-06-17 12:30 GMT

Dr Bryon A. Gentile, and Dr Dennis A. Tighe, at University of Massachusetts Medical School, Worcester, M have reported a case of Situs Inversus Totalis that has appeared in the New England Journal of Medicine.


Situs Inversus Totalis or Dextrocardia with situs inversus is a condition that is characterized by abnormal positioning of the heart and other internal organs. In people affected by dextrocardia, the tip of the heart points towards the right side of the chest instead of the left side. Situs inversus refers to the mirror-image reversal of the organs in the chest and abdominal cavity. Some affected people have no obvious signs or symptoms. However, a small percentage of people also have congenital heart defects, usually transposition of the great vessels. Dextrocardia with situs inversus can also be associated with primary ciliary dyskinesia (also known as Kartagener syndrome). Treatment typically depends on the heart or physical problems the person may have in addition to dextrocardia with situs inversus.


A 66-year-old man presented to the emergency department with a 3-day history of cough, congestion, and pain in his chest and the left side of his abdomen. Several months before presentation, he had immigrated to the United States after living in a refugee camp for 20 years. The results of the physical examination were notable for heart sounds best heard on the right side of the chest and for tenderness in the costochondral joints and the left upper quadrant on palpation.


An electrocardiogram showed right axis deviation, reverse precordial R-wave progression, and inverted P waves in leads I, aVL, and aVR. Findings on a chest radiograph included dextrocardia (Panel A), and computed tomography of the abdomen revealed mirror-image transposition of the abdominal organs (Panel B), confirming the presence of situs inversus totalis without acute pathologic features.



Situs inversus totalis can occur in isolation or in conjunction with primary ciliary dyskinesia. The patient had no history of recurrent respiratory infections suggestive of primary ciliary dyskinesia. Echocardiography revealed no structural abnormalities. A diagnosis of upper respiratory infection was made, and the musculoskeletal chest pain was treated with nonsteroidal anti-inflammatory drugs. The infection resolved several days after presentation.


For more details click on the link: DOI: 10.1056/NEJMicm1811002
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