External auditory canal obstruction due to tuberous sclerosis complex angiofibromas: a case report

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Küçük Resim

Tarih

2022

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Springer

Erişim Hakkı

info:eu-repo/semantics/openAccess

Özet

Background: Tuberous sclerosis complex (TSC), an autosomal dominant genetic disorder and auricula and external auditory canal (EAC) involvement, is rare. Surgical excision is rarely recommended for cutaneous lesions. Case presentation: A 31-year-old male patient was admitted with a complaint of left fullness, discharge, and conductive hearing loss. Symmetrical nodular cutaneous lesions on the malar region, tragus, and lateral portion of the EAC bilaterally were noted. The patient had diagnosed with TSC during adolescence clinically and genetically. Surgery was planned to obtain a favorable, self-cleaning EAC rather than total excision of angiofibromas. Angiofibromas on the EAC and tragus were excised. The defect was repaired by sliding a fasciocutaneous island flap inferiorly created in the preauricular area. No EAC stenosis or angiofibroma recurrence was observed during follow-up. Discussion: Surgical excision for this clinical entity provides satisfactory management even if it was not routinely recommended for other skin lesions.

Açıklama

Anahtar Kelimeler

Tuberous sclerosis complex, Neurocutaneous syndromes, Hamartoma, External ear, Island flap

Kaynak

Egyptian Journal of Otolaryngology

WoS Q Değeri

N/A

Scopus Q Değeri

Q4

Cilt

38

Sayı

1

Künye

İşlek, A. ve Şimşek, S. (2022). External auditory canal obstruction due to tuberous sclerosis complex angiofibromas: a case report. Egyptian Journal of Otolaryngology, 38(1), 62.