AI Article Synopsis
- Timely recognition of atypical Takayasu arteritis (TA) is essential, as unusual symptoms can complicate diagnosis.
- A specific case involved a 42-year-old male with pericardial effusion, where a CT angiogram confirmed the diagnosis of large vessel vasculitis.
- Successful management with immunosuppressive therapy highlights the need for collaborative care among various medical specialists to improve patient outcomes in TA.
Article Abstract
Key Clinical Message: Timely recognition of atypical Takayasu arteritis is crucial. Unusual presentations, such as pericardial effusion, can complicate diagnosis. CT angiogram aids in precise diagnosis, guiding targeted immunosuppressive therapy. Multidisciplinary collaboration is vital for comprehensive management, improving patient outcomes in this challenging condition.
Abstract: This case study highlights the diagnostic challenges posed by atypical presentations of Takayasu arteritis (TA), focusing on a 42-year-old male presenting with pericardial effusion. Despite inconclusive initial investigations, a CT angiogram revealed large vessel vasculitis, confirming TA. Management with immunosuppressive therapy led to clinical improvement. This case emphasize the importance of recognizing unusual manifestations of TA for timely diagnosis and appropriate treatment, emphasizing the role of multidisciplinary collaboration in optimizing patient outcomes.
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| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11147744 | PMC |
| http://dx.doi.org/10.1002/ccr3.9051 | DOI Listing |
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