دورية أكاديمية

Congenital orbital teratoma: a rare case with intracranial extension.

التفاصيل البيبلوغرافية
العنوان: Congenital orbital teratoma: a rare case with intracranial extension.
المؤلفون: Magalhães Paiva C; Department of Pediatric Surgery, Division of Pediatric Neurosurgery, Fernandes Figueira National Institutes of Health for Women, Children, and Adolescents, Oswaldo Cruz Foundation (IFF-Fiocruz), Rio de Janeiro, Brazil. magalhaespaiva@gmail.com., da Costa Pereira MR; Department of Pediatric Surgery, Division of Pediatric Neurosurgery, Fernandes Figueira National Institutes of Health for Women, Children, and Adolescents, Oswaldo Cruz Foundation (IFF-Fiocruz), Rio de Janeiro, Brazil., Bellas AR; Department of Pediatric Surgery, Division of Pediatric Neurosurgery, Fernandes Figueira National Institutes of Health for Women, Children, and Adolescents, Oswaldo Cruz Foundation (IFF-Fiocruz), Rio de Janeiro, Brazil., Protzenko T; Department of Pediatric Surgery, Division of Pediatric Neurosurgery, Fernandes Figueira National Institutes of Health for Women, Children, and Adolescents, Oswaldo Cruz Foundation (IFF-Fiocruz), Rio de Janeiro, Brazil.
المصدر: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery [Childs Nerv Syst] 2024 Sep; Vol. 40 (9), pp. 2653-2657. Date of Electronic Publication: 2024 Jul 01.
نوع المنشور: Case Reports; Journal Article; Review
اللغة: English
بيانات الدورية: Publisher: Springer International Country of Publication: Germany NLM ID: 8503227 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1433-0350 (Electronic) Linking ISSN: 02567040 NLM ISO Abbreviation: Childs Nerv Syst Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Berlin : Springer International, c1985-
مواضيع طبية MeSH: Teratoma*/surgery , Teratoma*/congenital , Teratoma*/diagnostic imaging , Teratoma*/pathology , Orbital Neoplasms*/surgery , Orbital Neoplasms*/congenital , Orbital Neoplasms*/diagnostic imaging , Orbital Neoplasms*/pathology, Humans ; Magnetic Resonance Imaging ; alpha-Fetoproteins/metabolism ; Tomography, X-Ray Computed ; Female ; Male ; Infant, Newborn
مستخلص: Introduction: Teratoma is the most common congenital tumor, but the orbital location is rare. It is composed of tissues from ectoderm, mesoderm, and endoderm.
Clinical Presentation: Congenital orbital teratoma commonly presents as unilateral proptosis, with rapid growth, leading to exposure keratopathy.
Diagnosis: Prenatal ultrasound may detect the orbital mass, computed tomography (CT) scans, and magnetic resonance (MR) imaging are better in demonstrating multilocular cystic and solid mass, without bone erosion. Laboratory tests should include alfa-fetoprotein (AFP) and B-human chorionic gonadotropin (B-HCG), and histopathologically, it contains all three germ cell layers components. The management is surgical removal of the lesion, the mature teratoma has a benign behavior, and the immature has a poor prognostic. We describe a rare case of congenital orbital teratoma with intracranial extension of the lesion, in which was treated with orbital exenteration. After surgery, AFP levels decreased, the middle face displacement has improved and development milestones were appropriate.
(© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
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فهرسة مساهمة: Keywords: Congenital orbital teratoma; Immature teratoma; Intracranial teratoma; Orbital exenteration
المشرفين على المادة: 0 (alpha-Fetoproteins)
تواريخ الأحداث: Date Created: 20240702 Date Completed: 20240814 Latest Revision: 20240814
رمز التحديث: 20240814
DOI: 10.1007/s00381-024-06510-9
PMID: 38953912
قاعدة البيانات: MEDLINE
الوصف
تدمد:1433-0350
DOI:10.1007/s00381-024-06510-9