Immature Orbital Teratoma With Intracranial Extension.

J Craniofac Surg

Division of Head and Neck Surgery, Instituto Nacional de Cancerología, Mexico City, Mexico Division of Oral and Maxillofacial Surgery, Clínica El Bosque. Bogotá, Colombia. Instituto Nacional de Cancerología, Mexico City, Mexico Division of Oral Pathology, Universidad El Bosque, Bogotá, Colombia. Oral and Maxillofacial Surgery Department, Clínica Fundadores Oral Pathology Residency Program, Universidad El Bosque, Bogotá, Colombia. Research Department, Institución Universitaria Colegios de Colombia, Bogotá Oral and Maxillofacial Surgery Department, Universidad del Sinú School of Dentistry, Montería, Colombia Universidad Evangélica de El Salvador School of Dentistry, San Salvador, El Salvador.

Published: September 2016

Download full-text PDF

Source
http://dx.doi.org/10.1097/SCS.0000000000002848DOI Listing

Publication Analysis

Top Keywords

immature orbital
4
orbital teratoma
4
teratoma intracranial
4
intracranial extension
4
immature
1
teratoma
1
intracranial
1
extension
1

Similar Publications

Background: Congenital intracranial immature teratoma is a rare tumor that is present in the first year of life. It is composed of three embryonic germ layers. These tumors are mainly manifested by hydrocephalus.

View Article and Find Full Text PDF

Congenital orbital teratoma: a rare case with intracranial extension.

Childs Nerv Syst

September 2024

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.

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.

View Article and Find Full Text PDF

Relapse of acute myeloid leukemia (AML) is highly aggressive and often treatment refractory. We analyzed previously published AML relapse cohorts and found that 40% of relapses occur without changes in driver mutations, suggesting that non-genetic mechanisms drive relapse in a large proportion of cases. We therefore characterized epigenetic patterns of AML relapse using 26 matched diagnosis-relapse samples with ATAC-seq.

View Article and Find Full Text PDF

Introduction: Fibrous dysplasia is a disorder in which normal bone is gradually replaced by immature fibro-osseous tissue, with an incidence of less than 7% of all benign bone tumors. The management of this disease is a challenge for plastic surgeons and neurosurgeons.

Goal: To describe the diagnostic, therapeutic, and outcome approach of patients with craniofacial fibrous dysplasia seen at the Plastic Surgery Service of the Hospital San José in Bogotá, Colombia.

View Article and Find Full Text PDF

Orbital Abscess Secondary to Nasolacrimal Duct Obstruction in an Extremely Preterm Infant.

Ophthalmic Plast Reconstr Surg

January 2024

Oculoplastic Division, Department of Ophthalmology, Bascom Palmer Eye Institute, University of Miami, Miami, Florida, U.S.A.

Orbital abscesses are rarely encountered in children younger than 1 year. The literature is limited to isolated case reports and a few case series. Most such cases are reported in infants born at term, with the earliest reported gestational birth age at 34 weeks.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!