Akademik Veri Yönetim Sistemi
EUROPEAN JOURNAL OF PLASTIC SURGERY, cilt.44, sa.3, ss.393-398, 2021 (ESCI)
The Binder syndrome is a congenital anomaly mostly seen in females characterized by a flat facial profile and flat nose with absent nasal spine, short columella, flat nasal dorsum, hypoplastic lower lateral cartilages (LLC) and septum, class-III malocclusion, and cleft lip and palate. A 26-year-old female patient with a Binder syndrome was referred to the clinic with a flat nasal dorsum, hypoplastic LLC, deformed nostrils, and hypoplastic columella. She had a history of bilateral cleft lip and palate, ocular strabismus, hypothyroidism, and growth retardation. An augmentation rhinoplasty with an open approach was performed in January 2019. The seventh costal cartilage and the rectus fascia were preferred as autologous grafts. An extended columellar strut graft was prepared and fixed to the nasal spine. Two lateral crural strut grafts was prepared and placed. The hypoplastic LLC were fixated to these grafts. A dorsal onlay graft was settled. Then, the diced cartilage-fascia (DC-F) graft was prepared and it was settled in over the nasal dorsum. A smaller and spherical DC-F graft was constructed to be placed over the extended columellar strut graft for increasing the tip projection. One-year postoperative results of this case confirm that the DC-F graft conserved its volume and shape. The growth retardation has not been described in Binder syndrome in the current literature, and this is the first case of nasal augmentation with DC-F graft in Binder syndrome. DC-F graft is a reliable alternative for the augmentation of the nasal dorsum in Binder syndrome. Level of evidence: Level V, therapeutic study.