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Sabeti, Nona, Hajmollarezaei, Ezat, Mohamad Pour, Ahmad, Pour Rajab, Emad. (1404). Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management. سامانه مدیریت نشریات علمی, 50(12), 873-876. doi: 10.30476/ijms.2025.105580.3943
Nona Sabeti; Ezat Hajmollarezaei; Ahmad Mohamad Pour; Emad Pour Rajab. "Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management". سامانه مدیریت نشریات علمی, 50, 12, 1404, 873-876. doi: 10.30476/ijms.2025.105580.3943
Sabeti, Nona, Hajmollarezaei, Ezat, Mohamad Pour, Ahmad, Pour Rajab, Emad. (1404). 'Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management', سامانه مدیریت نشریات علمی, 50(12), pp. 873-876. doi: 10.30476/ijms.2025.105580.3943
Sabeti, Nona, Hajmollarezaei, Ezat, Mohamad Pour, Ahmad, Pour Rajab, Emad. Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management. سامانه مدیریت نشریات علمی, 1404; 50(12): 873-876. doi: 10.30476/ijms.2025.105580.3943

Congenital Palatal Teratoma: A Rare Case of Postnatal Diagnosis and Multidisciplinary Management

Iranian Journal of Medical Sciences
مقاله 7، دوره 50، شماره 12، اسفند 2025، صفحه 873-876    اصل مقاله (1.22 M)
نوع مقاله: Case Report(s)
شناسه دیجیتال (DOI): 10.30476/ijms.2025.105580.3943
نویسندگان
Nona Sabeti1؛ Ezat Hajmollarezaei* 1؛ Ahmad Mohamad Pour2؛ Emad Pour Rajab2
1Supporting the Family and the Youth of Population Research Core, Department of Obstetrics and Gynecology, School of Medicine, Mashhad University of Medical Science, Mashhad, Iran
2Department of Pediatric Surgery, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
چکیده
Oropharyngeal teratoma (OPT) is a rare congenital tumor that may present either in isolation or in conjunction with craniofacial anomalies, often posing a major risk to infant survival. Recent advances in prenatal imaging, particularly high-resolution ultrasonography, have significantly improved the early detection and characterization of such tumors, enhancing clinical decision-making. Although prenatal sonography and MRI typically enable early diagnosis, the present study reported a case of OPT, diagnosed postpartum in an Iranian female infant weighing 4300 g. Despite the absence of prenatal diagnosis, the mass was successfully managed through prompt surgical intervention. The outcome was favorable, with no complications or recurrence. This case highlighted the critical role of early diagnosis and multidisciplinary perinatal planning in improving the prognosis of rare congenital tumors such as OPT.

تازه های تحقیق

Nona Sabeti (Google Scholar)

Ezat Hajmollarezaei (Google Scholar)

کلیدواژه‌ها
Oropharyngeal neoplasms؛ Teratoma؛ Congenital abnormalities؛ Prenatal diagnosis؛ Ultrasonography
سایر فایل های مرتبط با مقاله
مراجع
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