Pediatric hereditary angioedema presenting as recurrent episodic abdominal pain and vomiting: Challenges in diagnosis and management

Recurrent episodic abdominal pain and vomiting, with symptom-free intervals between attacks, represent common and often challenging presentations in children, typically leading to extensive workups without a clear etiology, as standard diagnostic algorithms fail to include rare systemic conditions. We present the challenging diagnostic odyssey of a pediatric patient (symptom onset at age 4 years; diagnosis at age 8), culminating in an unexpected diagnosis of hereditary angioedema, a critical etiology often omitted from differentials. This case underscores a key gap in current clinical pathways and serves to expand the diagnostic consideration for specialists managing unexplained recurrent episodic abdominal symptoms.

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Publication Details

Journal
JPGN Reports
Published
2026-08-14
DOI
https://doi.org/10.1002/jpr3.70232
Primary Topic
Coagulation, Bradykinin, Polyphosphates, and Angioedema
Type
article
Field-Weighted Citation Impact
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article

Pediatric hereditary angioedema presenting as recurrent episodic abdominal pain and vomiting: Challenges in diagnosis and management

Verónica Busoni, Julio Busaniche, Judith Cohen Sabban, María Soledad Arcucci et al.
JPGN Reports
Coagulation, Bradykinin, Polyphosphates, and Angioedema
article

Pediatric hereditary angioedema presenting as recurrent episodic abdominal pain and vomiting: Challenges in diagnosis and management

Verónica Busoni, Julio Busaniche, Judith Cohen Sabban, María Soledad Arcucci, Valentina Riveros, Jhoanna Adauto Luizaga, Claudio Alberto Salvador Parisi, Agustina Venditti, Giancarlo Testa
article en

Abstract

Recurrent episodic abdominal pain and vomiting, with symptom-free intervals between attacks, represent common and often challenging presentations in children, typically leading to extensive workups without a clear etiology, as standard diagnostic algorithms fail to include rare systemic conditions. We present the challenging diagnostic odyssey of a pediatric patient (symptom onset at age 4 years; diagnosis at age 8), culminating in an unexpected diagnosis of hereditary angioedema, a critical etiology often omitted from differentials. This case underscores a key gap in current clinical pathways and serves to expand the diagnostic consideration for specialists managing unexplained recurrent episodic abdominal symptoms.

JPGN Reports
Hospital Italiano de Buenos Aires (AR), Hospital General de Niños Ricardo Gutierrez (AR)
Good health and well-being
Openalex Percentile: Top 10%
Coagulation, Bradykinin, Polyphosphates, and Angioedema
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