Thoracoabdominal compartment syndrome complicating right-sided diaphragmatic eventration with co-existent unilateral renal agenesis

Authors

DOI:

https://doi.org/10.4322/acr.2020.155

Keywords:

Diaphragmatic Eventration, Compartment Syndrome, Hereditary renal agenesis

Abstract

Diaphragmatic eventration (DE) associated with intestinal malrotation and renal agenesis is a rare entity. The authors report a case of a 69-year-old man who had symptoms of heart failure. He had a previous imaging diagnosis of right diaphragmatic eventration and dilated cardiomyopathy. He died on the second day after the hospital admission and had a post mortem examination that confirmed complete right diaphragmatic eventration, intestinal malrotation, left renal agenesis, dilated cardiomyopathy, and anteriorly rotated right kidney and had findings suggestive of a thoracoabdominal compartment syndrome. Thoracoabdominal compartment syndrome is described as transmission of abdominal pressure through a defective diaphragm causing compression of the hemithorax viscera and mediastinal shift with a hemodynamic alteration. The association of these anomalies is rare, and the possibility of this finding in a patient with eventration should always be considered.

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Published

2020-07-06

Issue

Section

Article / Autopsy Case Report

How to Cite

Omenai, S. A., Adebowale, E. O., & Nwanji, I. D. (2020). Thoracoabdominal compartment syndrome complicating right-sided diaphragmatic eventration with co-existent unilateral renal agenesis. Autopsy and Case Reports, 10(2), e2020155. https://doi.org/10.4322/acr.2020.155