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  2. Keyword: Eisenmenger Complex
Figure 1
ABC
Anatomopathological Session

Case 1/2016 – 56-Year-Old Male with Atrial Septal Defect, Pulmonary Arterial Hypertension, Hospitalized Due to Eisenmenger Syndrome

Carolina Santana et al. Antonio Augusto B. Lopes Antonio Fernando Lins de Paiva Luiz Alberto Benvenuti

Postmortem examination

The heart was enlarged and globoid, weighing 832 g. On gross examination, the RV was prominent. The opening of the cavities evidenced eccentric hypertrophy of the four chambers, mainly the right ones, which showed marked dilation. A large ASD was identified in the fossa ovalis (ostium secundum type), measuring 3.5 x 3.0 cm (). The ventricular septum was intact, no other heart malformation being identified. The microscopic examination revealed hypertrophy of the cardiomyocytes and myocardial interstitial fibrosis in both ventricles, with no evidence of ischemic lesions (infarction). The pulmonary trunk was dilated (diameter of 4.0 cm) and showed complicated atherosclerosis, with calcified areas. The right pulmonary artery showed calcified atherosclerosis, organized partial thrombosis, and markedly dilation of its parenchymatous branches. The process was similar in the left lung, but the thrombosis was more extensive, affecting numerous arterial branches, in an occlusive way, including the pulmonary hilum (). The microscopic examination of the lungs confirmed the extensive organizing arterial thrombosis detected on gross examination, in addition to revealing: organized and rechanneled arteriolar thrombosis (); recent focal thrombosis of a small artery and small hemorrhagic infarction in the lower lobe of the right lung (); areas of alveolar hemorrhage; anthracosis; microscopic evidence of chronic bronchitis; and diffuse pulmonary emphysema. In addition, a small in situ adenocarcinoma was found in the right lung, measuring 9 mm. Moderate aorta atherosclerosis was identified, with calcified plaques. Neither pneumothorax nor bronchopneumonia were evidenced.

[…]

  • Eisenmenger Complex
  • Heart Defects, Congenital
  • Heart Septal Defects, Atrial
  • Hypertension Pulmonary
  • Lung Diseases, Obstructive
  • Pulmonary embolism
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Creative Commons Attribution (CC BY) Creative Commons license
01/03/2016 DOI: 10.5935/abc.20160035 Views 2

How to cite this article

EndNote RIS

Electronic Document Format (Vancouver)

Santana C, Lopes AAB, Paiva AFL, Benvenuti LA. Case 1/2016 – 56-Year-Old Male with Atrial Septal Defect, Pulmonary Arterial Hypertension, Hospitalized Due to Eisenmenger Syndrome. Arquivos Brasileiros de Cardiologia 2016;106(3):250-8.

Electronic Document Format (ABNT)

Santana, Carolina; Lopes, Antonio Augusto B.; Paiva, Antonio Fernando Lins de; Benvenuti, Luiz Alberto. Case 1/2016 – 56-Year-Old Male with Atrial Septal Defect, Pulmonary Arterial Hypertension, Hospitalized Due to Eisenmenger Syndrome. Arquivos Brasileiros de Cardiologia, v. 106, n. 3, p. 250-258, Feb. 2016.

Electronic Document Format (APA)

Santana, C., Lopes, A. A. B., Paiva, A. F. L. , & Benvenuti, L. A. (2016). Case 1/2016 – 56-Year-Old Male with Atrial Septal Defect, Pulmonary Arterial Hypertension, Hospitalized Due to Eisenmenger Syndrome. Arquivos Brasileiros de Cardiologia, 106(3), 250-258.

Electronic Document Format (ISO)

Santana, Carolina and Lopes, Antonio Augusto B. and Paiva, Antonio Fernando Lins de and Benvenuti, Luiz Alberto. Case 1/2016 – 56-Year-Old Male with Atrial Septal Defect, Pulmonary Arterial Hypertension, Hospitalized Due to Eisenmenger Syndrome. Arquivos Brasileiros de Cardiologia [online]. 2016, vol. 106, n. 3, [cited 2026-10-14], pp. 250-258. Available from: <https://journals.cardiol.br/en/article/case-1-2016-56-year-old-male-with-atrial-septal-defect-pulmonary-arterial-hypertension-hospitalized-due-to-eisenmenger-syndrome/>. ISSN 0066-782X

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