A Huge Thoracic Aortic Aneurysm as a Rare Complication of Hyperimmunoglobulin E Syndrome.

Leila Bigdelu, Ossama Maadarani, Ali Azari, Ali Heidari-Bakavoli, Zahra Oskoueyan, Zouhair Bitar

Abstract readCase Reports

In one paragraph

Article in JACC. Case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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5 · Who and what money

Authors and funding

6 authors.

Leila BigdeluVascular and Endovascular Surgery Research Center, Mashhad University of Medical Sciences, Mashhad, Iran. Electronic address: omaadarani@kockw.com.

Ossama MaadaraniCritical Care Unit, Internal Medical Department, Ahmadi Hospital-Kuwait Oil Company, Al Ahmadi, Kuwait.

Ali AzariVascular and Endovascular Surgery Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Ali Heidari-BakavoliDepartment of Imaging, Razavi Hospital, Mashhad, Iran.

Zahra OskoueyanVascular and Endovascular Surgery Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.

Zouhair BitarCritical Care Unit, Internal Medical Department, Ahmadi Hospital-Kuwait Oil Company, Al Ahmadi, Kuwait.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperimmunoglobulin E syndromes (HIES) are a heterogeneous group of primary immunodeficiencies sharing manifestations including recurrent lung infection, staphylococcal skin abscesses, eczema, and significantly raised serum levels of immunoglobulin E. Arterial aneurysms are among the rare vascular manifestations of HIES that may lead to devastating outcomes. We present a case of a 17-year-old girl who had a known history of HIES since childhood. She manifested a recurrent chest infection and skin rash, and it was discovered that she had a large thoracic descending aortic aneurysm, which required surgical repair to prevent devastating complications.

Indexed as

aortacomputed tomographyechocardiography

Identifiers

PMID40973336

DOI10.1016/j.jaccas.2025.104911

PMCPMC12478479

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