ISSN: 1308-5727 | E-ISSN: 1308-5735
Volume: 16 Issue: 3 Year: 2024
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Abstracting & Indexing
Turkish Society for Pediatric Endocrinology and Diabetes
A Potentially Fatal Outcome of Oral Contraceptive Therapy: Estrogen-Triggered Hereditary Angioedema in an Adolescent [J Clin Res Pediatr Endocrinol]
J Clin Res Pediatr Endocrinol. 2023; 15(2): 210-213 | DOI: 10.4274/jcrpe.galenos.2021.2021.0053

A Potentially Fatal Outcome of Oral Contraceptive Therapy: Estrogen-Triggered Hereditary Angioedema in an Adolescent

Uğur Berkay Balkancı1, Demet Demirkol2, Gül Yeşiltepe Mutlu3, Esra Birben4, Özge Soyer4, Özlem Yılmaz5, Cansın Saçkesen5
1Koç University Faculty of Medicine, İstanbul, Turkey
2Koç University Faculty of Medicine, Department of Pediatric Intensive Care; İstanbul University, İstanbul Faculty of Medicine, Department of Pediatric Intensive Care, İstanbul, Turkey
3Koç University Faculty of Medicine, Department of Pediatric Endocrinology, İstanbul, Turkey
4Hacettepe University Faculty of Medicine, Department of Pediatric Allergy, Ankara, Turkey
5Koç University Faculty of Medicine, Department of Pediatric Allergy, İstanbul, Turkey

Hereditary angioedema (HAE) is characterized by recurrent angioedema attacks with no urticaria. This disease has a high mortality due to asphyxia. Level of complement component 4 (C4), C1 esterase inhibitor (C1-INH) level and function, and genetic mutations determine different endotypes of HAE. Clinical presentation and the triggers of vasogenic edema may change according to the endotypes. An adolescent girl with oligomenorrhea, obesity, hirsutism, and acanthosis nigricans was diagnosed with polycystic ovary syndrome and prescribed ethinyl estradiol and cyproterone acetate containing oral contraceptive (OC). On the sixteenth day of treatment, she developed angioedema of the face, neck, and chest leading to dyspnea. Adrenaline, antihistamine, and corticosteroid treatments were ineffective. In the family history, the patient’s mother and two cousins had a history of angioedema. C1-INH concentrate was administered with a diagnosis of HAE. C4 and C1-INH level and activity were normal. Genetic analysis identified a mutation in the factor 12 (F12) gene, and the diagnosis of F12-related HAE was made. OC treatment was discontinued. She has had no additional angioedema attacks in the follow-up period of two years. OC containing estrogen may induce the life-threatening first attack of F12-related HAE even in children. Recurring angioedema attacks in the family should be asked before prescribing estrogen-containing OC pills.

Keywords: Hereditary angioedema type 3, hereditary angioedema, angioedema, factor 12, polycystic ovary syndrome

Corresponding Author: Cansın Saçkesen, Türkiye
Manuscript Language: English
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