The swell within: a rare case of type 1 hereditary angioedema.

Proc (Bayl Univ Med Cent)May 11, 2026 (epub)
Case ReportAllergy & ImmunologyOpen access

Desai Jay Manharlal, Naman Singh, Manik Gakhar et al.

✦ AI-curated · Sources linked

Case in brief

A 20-year-old woman presented with facial swelling and recurrent abdominal pain. Evaluation revealed type 1 hereditary angioedema due to low levels of C1 esterase inhibitor. Following timely diagnosis and personalized management, her overall well-being improved significantly. This case underscores the importance of recognizing hereditary angioedema in patients with unexplained recurrent symptoms.

Diagnostic / clinical pearl

Clinicians should consider hereditary angioedema in patients with recurrent angioedema and abdominal pain, even in the absence of cutaneous symptoms.

Why it matters

Heightened awareness of hereditary angioedema can lead to timely diagnosis and management, reducing morbidity and preventing misdiagnosis in young patients.

Source

Published in Proc (Bayl Univ Med Cent). This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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