Retrospective Review of Craniosynostosis Cases: Bursa Uludağ University Experience

Rabia Nur Balçın; Hanside Setenay Ünal; Pınar Eser Ocak; Mevlüt Özgür Taşkapılıoğlu

Makale detayları

Retrospective Review of Craniosynostosis Cases: Bursa Uludağ University Experience

Yazarlar:

Rabia Nur Balçın | Hanside Setenay Ünal | Pınar Eser Ocak | Mevlüt Özgür Taşkapılıoğlu

Yayıncı:

Bursa Uludağ University

Ana Başlıklar:

Cerrahi (Diğer)

Dergi:

Uludağ Üniversitesi Tıp Fakültesi Dergisi Vol.50 Issue 1, pp.85-88

Belge Tipi:

Makale

Yayın Tarihi:

5/2024

Belge Dili:

Türkçe

Document ID (Org No.):

2001317385

pISSN:

1300-414X

Anahtar kelimeler:

Özet:

 Craniosynostosis is a developmental craniofacial anomaly that causes neuronal developmental problems and abnormal skull shape. In this study, the patient files of pediatric patients who were followed and treated in our clinic between January 2005 and December 2022 were retrospectively evaluated. 94 patients were included in our study. 57 60.6 of the patients were male and 37 39.4 were female. 45 47.9 cases were operated for scaphocephaly, 31 33 for trigonocephaly, and 12 12.8 for plagiocephaly. There were 4 4.25 cases of syndromic craniosynostosis. Median operative time was 95 minutes. A significant correlation was found between operation time and hospitalization time. Postoperative complications developed in 3 3.2 cases. Mortality was observed in the early postoperative period in 3 3.2 cases. Craniosynostosis, one of the main pathologies of pediatric neurosurgery, is not just a cosmetic problem; It is a pathology that needs to be treated at the right time to ensure neuronal development. It should be kept in mind that it is a serious pathology that can cause mortality and morbidity despite developing surgical techniques.

 Craniosynostosis is a developmental craniofacial anomaly that causes neuronal developmental problems and abnormal skull shape. In this study, the patient files of pediatric patients who were followed and treated in our clinic between January 2005 and December 2022 were retrospectively evaluated. 94 patients were included in our study. 57 60.6 of the patients were male and 37 39.4 were female. 45 47.9 cases were operated for scaphocephaly, 31 33 for trigonocephaly, and 12 12.8 for plagiocephaly. There were 4 4.25 cases of syndromic craniosynostosis. Median operative time was 95 minutes. A significant correlation was found between operation time and hospitalization time. Postoperative complications developed in 3 3.2 cases. Mortality was observed in the early postoperative period in 3 3.2 cases. Craniosynostosis, one of the main pathologies of pediatric neurosurgery, is not just a cosmetic problem; It is a pathology that needs to be treated at the right time to ensure neuronal development. It should be kept in mind that it is a serious pathology that can cause mortality and morbidity despite developing surgical techniques.

 Craniosynostosis is a developmental craniofacial anomaly that causes neuronal developmental problems and abnormal skull shape. In this study, the patient files of pediatric patients who were followed and treated in our clinic between January 2005 and December 2022 were retrospectively evaluated. 94 patients were included in our study. 57 60.6 of the patients were male and 37 39.4 were female. 45 47.9 cases were operated for scaphocephaly, 31 33 for trigonocephaly, and 12 12.8 for plagiocephaly. There were 4 4.25 cases of syndromic craniosynostosis. Median operative time was 95 minutes. A significant correlation was found between operation time and hospitalization time. Postoperative complications developed in 3 3.2 cases. Mortality was observed in the early postoperative period in 3 3.2 cases. Craniosynostosis, one of the main pathologies of pediatric neurosurgery, is not just a cosmetic problem; It is a pathology that needs to be treated at the right time to ensure neuronal development. It should be kept in mind that it is a serious pathology that can cause mortality and morbidity despite developing surgical techniques.

 Kraniosinostoz, beyin gelişiminde bozulmaya ve anormal kafatası şekline neden olan gelişimsel bir kraniofasiyal anomalidir. Bu çalışmamızda kliniğimizde Ocak 2005- Aralık 2022 tarihleri arasında takip ve tedavi edilen pediatrik hastaların dosyaları retrospektif olarak incelenmiştir. Çalışmamıza 94 hasta dahil edilmiştir. Hastaların 57 60,6 tanesi erkek, 37si 39,4 kadındı. 45 47,9 olgu skafosefali, 31 33 olgu trigonosefali, 12 plagiosefali 12,8 nedeni ile opere edildi. 4 4,25 sendromik kraniosinostoz olgusu mevcuttu. Median operasyon süresi 95 dakikaydı. Operasyon süresi ile yatış süresi arasında anlamlı korelasyon saptandı. 3 3,2 olguda postoperatif komplikasyon gelişti. 3 3.2 olguda postoperatif erken dönemde mortalite gözlendi. Pediatrik nöroşirürjinin ana patolojilerinden biri olan kraniosinositoz sadece kozmetik bir sorun değil; nöronal gelişimin sağlanması için doğru zamanda tedavi edilmesi gereken bir patolojidir. Gelişen cerrahi tekniklere rağmen mortalite ve morbiditelere neden olabilecek ciddi bir patoloji olduğu akılda tutulmalıdır.

Makale detayları

Retrospective Review of Craniosynostosis Cases: Bursa Uludağ University Experience

Yazarlar:

Rabia Nur Balçın | Hanside Setenay Ünal | Pınar Eser Ocak | Mevlüt Özgür Taşkapılıoğlu

Yayıncı:

Bursa Uludağ University

Ana Başlıklar:

Cerrahi (Diğer)

Dergi:

Uludağ Üniversitesi Tıp Fakültesi Dergisi Vol.50 Issue 1, pp.85-88

Belge Tipi:

Makale

Yayın Tarihi:

5/2024

Belge Dili:

Türkçe

Document ID (Org No.):

2001317385

pISSN:

1300-414X

Craniosynostosis

scaphocephaly

trigonocephalyKraniosinositoz

skafosefali

trigonosefali

Sayı

Makale detayları

Retrospective Review of Craniosynostosis Cases: Bursa Uludağ University Experience

Yazarlar: Rabia Nur Balçın | Hanside Setenay Ünal | Pınar Eser Ocak | Mevlüt Özgür Taşkapılıoğlu

Yayıncı: Bursa Uludağ University

Ana Başlıklar: Cerrahi (Diğer)

Dergi: Uludağ Üniversitesi Tıp Fakültesi Dergisi Vol.50 Issue 1, pp.85-88

Belge Tipi: Makale

Yayın Tarihi: 5/2024

Belge Dili: Türkçe

Document ID (Org No.): 2001317385

pISSN: 1300-414X

Craniosynostosis

scaphocephaly

trigonocephalyKraniosinositoz

skafosefali

trigonosefali

Sayı

Yazarlar:

Rabia Nur Balçın | Hanside Setenay Ünal | Pınar Eser Ocak | Mevlüt Özgür Taşkapılıoğlu

Yayıncı:

Bursa Uludağ University

Ana Başlıklar:

Cerrahi (Diğer)

Dergi:

Uludağ Üniversitesi Tıp Fakültesi Dergisi Vol.50 Issue 1, pp.85-88

Belge Tipi:

Makale

Yayın Tarihi:

5/2024

Belge Dili:

Türkçe

Document ID (Org No.):

2001317385

pISSN:

1300-414X