Variant cardiac transthyretin amyloidosis presenting as hypertrophic cardiomyopathy with left ventricular outflow tract obstruction: a case report
The present case illustrates that LVOTO can occur in patients with ATTRv. While cardiac imaging pointed towards sarcomeric HCM, the coexisting red flags initiated re-evaluation of the diagnosis suggesting cardiac amyloidosis as a potential cause. The presence of non-cardiac red flags of transthyretin amyloidosis (ATTR) should initiate specific diagnostic work-up even if ATTR is unlikely based on cardiac imaging.
Authors
- Andreas Zirlik (ORCID: https://orcid.org/0000-0001-6290-3297)
- Viktoria Höller (ORCID: https://orcid.org/0009-0001-7024-2131)
- Nicolas Verheyen (ORCID: https://orcid.org/0000-0001-7414-4056)
- Johannes Schmid (ORCID: https://orcid.org/0000-0001-8884-7924)
- Viktoria Santner (ORCID: https://orcid.org/0000-0001-8569-3683)
Institutions
- Medical University of Graz (AT)
Publication Details
- Journal
- European Heart Journal - Case Reports
- Published
- 2025-01-23
- DOI
- https://doi.org/10.1093/ehjcr/ytaf029
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00