# SARS-CoV-2 Coronavirus Disease in Patients with Underlying Congenital Inferior Vena Cava Anomalies

**Authors:** Fadia Salman, Pierfrancesco Antonio Annuvolo, Marta Minucci, Francesco Sposato, Ottavia Borghese, Yamume Tshomba

PMC · DOI: 10.3390/biomedicines13061336 · Biomedicines · 2025-05-29

## TL;DR

This paper discusses how a 36-year-old man with a rare heart condition developed severe blood clots after contracting COVID-19.

## Contribution

The paper presents a rare case linking congenital cardiovascular anomalies with severe DVT following COVID-19.

## Key findings

- Patients with congenital cardiovascular anomalies may develop extensive DVT after contracting COVID-19.
- Anticoagulation treatment must be carefully tailored to balance clot prevention and bleeding risks in these patients.

## Abstract

Background: COVID-19-related deep vein thrombosis (DVT) in patients with pre-existing congenital anomalies or genetic diseases of the cardiovascular system has been rarely reported, and a clear definition of best treatment in this setting remains undefined. Methods: We report the rare case of a 36-year-old male patient affected with a congenital cardiovascular anomaly, presenting extensive venous thrombosis following COVID-19-induced coagulopathy. An insight into current treatment strategies in this setting is also reported. Results and Conclusions: COVID-19 disease appears to be a determining factor in the development of extensive DVT in patients with congenital anomalies and genetic disorders. Anticoagulation should be tailored to the individual risk factors, balancing the risk-benefit between prevention of VTE and hemorrhagic complications.

## Linked entities

- **Diseases:** congenital cardiovascular anomaly (MONDO:0024239), COVID-19 (MONDO:0100096)

## Full-text entities

- **Diseases:** hemorrhagic complications (MESH:D006470), Congenital Inferior Vena Cava Anomalies (MESH:C563013), coagulopathy (MESH:D001778), COVID-19 (MESH:D000086382), DVT (MESH:D020246), congenital cardiovascular anomaly (MESH:D018376), congenital anomalies (MESH:D000013), genetic diseases (MESH:D030342)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12189561/full.md

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12189561/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12189561/full.md

---
Source: https://tomesphere.com/paper/PMC12189561