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Unique Presentation of Pediatric Orbital Varix.
Ophthalmic Plast Reconstr Surg
January 2025
Department of Ophthalmology, University of Kentucky College of Medicine, Lexington, Kentucky, U.S.A.
A 2-year-old girl initially presented with an enlarging and fluctuating mass resembling a bruise several months after orbital trauma. CT imaging showed soft tissue contusion and possible hematoma, without cystic characteristics. Surgical excision was conducted and immunohistochemistry staining revealed CD34+ endothelium.
View Article and Find Full Text PDFRegression of bilateral persistent primitive ophthalmic artery: a case report.
Surg Radiol Anat
December 2024
Department of Neurosurgery, Nagoya University of Graduate School of Medicine, Tsurumai-Cho 65, Showa-Ku, Nagoya, Aichi, Japan.
Purpose: We report a case of regression of a 2-year-old girl with bilateral primitive ophthalmic arteries (POAs).
Case Report: The patient presented with a headache and had no visual impairment or visual field abnormalities. Magnetic resonance angiography (MRA) revealed arteries originating bilaterally from the cavernous internal carotid artery segments, diagnosed as persistent POAs.
Ingestion of Multiple Magnets by Children: Diagnosis and Management When Ingestion is not Witnessed.
Ann Ital Chir
December 2024
General and Thoracic Pediatric Surgery Unit, Bambino Gesù Children's Hospital, IRCCS, 00165 Rome, Italy.
Aim: Foreign body ingestion, particularly that of magnets, is a significant issue for children aged 6 months to 3 years due to their prevalence in toys and household items. Most ingested foreign bodies pass naturally, but 10%-20% of such cases require endoscopic removal, and <1% require surgery.
Case Presentation: A 2-year-old girl presented with abdominal pain, nausea, and vomiting.
Genetic analysis of partial duplication of the long arm of chromosome 16.
BMC Med Genomics
December 2024
Department of Pediatrics, Sichuan Provincial Woman's and Children's Hospital, The Affiliated Women's and Children's Hospital of Chengdu Medical College, Chengdu, China.
Background: Pure partial trisomy 16q12.1q22.1 is a rare chromosome copy number variant (CNV).
View Article and Find Full Text PDFSurgical management of a huge mediastinal mature teratoma in a 2-year-old girl: a case report.
Gen Thorac Cardiovasc Surg Cases
December 2024
Department of Surgery II, Faculty of Medicine, Yamagata University, 2-2-2 Iida-Nishi, Yamagata, Japan.
Background: Mature teratomas are benign cystic tumors that are most commonly asymptomatic. However, in some cases, mediastinal teratomas rupture the lungs and mediastinum with potentially fatal outcomes. Herein, we report a case of a large mediastinal mature teratoma that expanded to the entire left hemithorax in a child with common cold-like symptoms.
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