An Intriguing Case of Infrarenal Aortic Hypoplasia

Infrarenal aortic hypoplasia is a very rare anomaly of the vascular tree characterised by diffuse stenosis of the infrarenal abdominal aorta. The pathogenesis of this condition seems to be unclear despite the advancements of vascular surgery. In general, the most common presenting symptom is claudic...

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Main Authors: Dilip Vincent, Rohini Avavantsa, Kabekkodu Venkata Tejaswi
Format: Article
Language:English
Published: JCDR Research and Publications Private Limited 2020-03-01
Series:Journal of Clinical and Diagnostic Research
Subjects:
Online Access:https://jcdr.net/articles/PDF/13547/43378_CE[Ra1]_F(KM)_PF1(AG_SHU)_PFA(SL)_PB(AG_KM)_PN(SL).pdf
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spelling doaj-a739636b2a2e47709762fa498a0b5b142020-11-25T02:38:58ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2020-03-01143TD01TD0210.7860/JCDR/2020/43378.13547An Intriguing Case of Infrarenal Aortic HypoplasiaDilip Vincent0Rohini Avavantsa1Kabekkodu Venkata Tejaswi2Junior Resident, Department of Radiodiagnosis, K S Hegde Medical Academy, Mangalore, Karnataka, India.Associate Professor, Department of Radiodiagnosis, K S Hegde Medical Academy, Mangalore, Karnataka, India.Senior Resident, Department of Radiodiagnosis, K S Hegde Medical Academy, Mangalore, Karnataka, India.Infrarenal aortic hypoplasia is a very rare anomaly of the vascular tree characterised by diffuse stenosis of the infrarenal abdominal aorta. The pathogenesis of this condition seems to be unclear despite the advancements of vascular surgery. In general, the most common presenting symptom is claudication occurring in 3rd to 4th decade of life. Here, a rare and interesting case of infrarenal aortic hypoplasia is reported in a 32 year-old female patient who presented with a history of low backache and bilateral intermittent lower extremity claudication. Using Doppler ultrasonography and computed tomographic angiography, we could demonstrate the abrupt termination of the infrarenal aorta with collateral reformation.https://jcdr.net/articles/PDF/13547/43378_CE[Ra1]_F(KM)_PF1(AG_SHU)_PFA(SL)_PB(AG_KM)_PN(SL).pdfabdominal aortic hypoplasiaaortic coarctationintermittent claudication
collection DOAJ
language English
format Article
sources DOAJ
author Dilip Vincent
Rohini Avavantsa
Kabekkodu Venkata Tejaswi
spellingShingle Dilip Vincent
Rohini Avavantsa
Kabekkodu Venkata Tejaswi
An Intriguing Case of Infrarenal Aortic Hypoplasia
Journal of Clinical and Diagnostic Research
abdominal aortic hypoplasia
aortic coarctation
intermittent claudication
author_facet Dilip Vincent
Rohini Avavantsa
Kabekkodu Venkata Tejaswi
author_sort Dilip Vincent
title An Intriguing Case of Infrarenal Aortic Hypoplasia
title_short An Intriguing Case of Infrarenal Aortic Hypoplasia
title_full An Intriguing Case of Infrarenal Aortic Hypoplasia
title_fullStr An Intriguing Case of Infrarenal Aortic Hypoplasia
title_full_unstemmed An Intriguing Case of Infrarenal Aortic Hypoplasia
title_sort intriguing case of infrarenal aortic hypoplasia
publisher JCDR Research and Publications Private Limited
series Journal of Clinical and Diagnostic Research
issn 2249-782X
0973-709X
publishDate 2020-03-01
description Infrarenal aortic hypoplasia is a very rare anomaly of the vascular tree characterised by diffuse stenosis of the infrarenal abdominal aorta. The pathogenesis of this condition seems to be unclear despite the advancements of vascular surgery. In general, the most common presenting symptom is claudication occurring in 3rd to 4th decade of life. Here, a rare and interesting case of infrarenal aortic hypoplasia is reported in a 32 year-old female patient who presented with a history of low backache and bilateral intermittent lower extremity claudication. Using Doppler ultrasonography and computed tomographic angiography, we could demonstrate the abrupt termination of the infrarenal aorta with collateral reformation.
topic abdominal aortic hypoplasia
aortic coarctation
intermittent claudication
url https://jcdr.net/articles/PDF/13547/43378_CE[Ra1]_F(KM)_PF1(AG_SHU)_PFA(SL)_PB(AG_KM)_PN(SL).pdf
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