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Background: Skull base reconstruction presents a number of challenges from anatomical and functional perspectives. This is especially the case with large anterior skull base defects with compromised recipient beds from repeated infection, multiple surgeries, or previous radiation. The purpose of the study was to demonstrate the use of the titanium mesh/radial forearm free flap (RFFF) mesh sandwich for reconstruction of large anterior skull base defects with a poor recipient bed or excessive bony defect.
Methods: Retrospective case series of 3 patients with complex anterior skull base defects reconstructed with a titanium mesh/RFFF mesh sandwich technique.
Results: Reconstruction of 3 cases using the titanium mesh/RFFF sandwich technique resulted in definitive treatment with no recurrent cerebral spinal fluid leaks, meningitis, or complications.
Conclusions: The titanium mesh/RFFF sandwich is an excellent reconstructive option for large anterior skull base defects with a poor recipient bed. This approach is facilitated using a combined open and endonasal endoscopic approach in a multidisciplinary team composed of head and neck surgery, rhinology, and neurosurgery.
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http://dx.doi.org/10.1097/SCS.0b013e3182653f29 | DOI Listing |
Pediatr Dev Pathol
September 2025
The Hospital for Sick Children, Division of Pathology, Toronto, Canada.
Background: Rhabdomyosarcoma (RMS) is the most common soft tissue sarcoma of childhood. For stratification purposes, rhabdomyosarcoma is classified into fusion-positive RMS (alveolar rhabdomyosarcoma) and fusion-negative RMS (embryonal or spindle cell/sclerosing, FN-RMS) subtypes according to its fusion status. This study aims to highlight the pathologic and molecular characteristics of a cohort of FN-RMS using a targeted NGS RNA-Seq assay.
View Article and Find Full Text PDFJ Leukoc Biol
September 2025
School of Pharmacy and Medical Science and Central Facility for Genomics, Griffith University, Parklands Drive, QLD, Australia.
There is limited understanding of the impact of anti-IL5 treatment on nasal polyp tissue biology in chronic rhinosinusitis with nasal polyps (CRSwNP). This study examined nasal polyp tissue cellular proteome and transcriptome responses to anti-IL5 treatment in CRSwNP utilising spatial profiling. GeoMx™ Digital Spatial Profiling (DSP) of 80 proteins and 1,833 mRNA targets in the polyp stroma and the whole transcriptome (18,815 mRNA targets) in polyp epithelia was undertaken on sinonasal biopsies collected from 20 individuals with eosinophilic CRSwNP before and after 16 and 24 weeks of mepolizumab treatment.
View Article and Find Full Text PDFOtolaryngol Head Neck Surg
September 2025
Department of Otolaryngology-Head and Neck Surgery, West Virginia University, Morgantown, West Virginia, USA.
Socioeconomic and neighborhood disadvantages have been increasingly investigated for their associations with outcomes in a variety of otolaryngologic conditions. The aim of this study is to explore the role of area deprivation index (ADI) on the hospital length of stay and 30-day readmission following endoscopic endonasal skull base surgery (EESBS). We performed a cross-sectional study of all patients who underwent EESBS between August 2020 and April 2024 at an academic institution.
View Article and Find Full Text PDFFacial Plast Surg
September 2025
ENT, Son Espases University Hospital, Palma, Spain.
Introduction Postoperative edema and fibrosis are key concerns following rhinoplasty, affecting outcomes and patient satisfaction. Triamcinolone acetonide (TA) is used for its proven anti-inflammatory and anti-fibrotic effects. Objective This study aims to evaluate the efficacy, usage profile, and safety of TA injections after rhinoplasty, focusing on postoperative edema and supratip fullness.
View Article and Find Full Text PDFCureus
August 2025
Pathology, Hanoi Medical University, Hanoi, VNM.
Parapharyngeal space (PPS) tumors are extremely rare in the pediatric population, accounting for a small fraction of all head and neck neoplasms. The majority of neoplasms in the PPS are benign tumors. We present a case of an eight-year-old male with a large PPS ganglioneuroma, who presented with a neck mass that had been progressing over five years with no symptoms of dysphasia.
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