98%
921
2 minutes
20
Objective: Traditionally, locally advanced scalp malignancies have been managed through composite, full-thickness calvarial resection. The aim of this study is to explore the oncologic outcomes of partial calvarial resection for locally invasive scalp malignancies without medullary space invasion, employing a burr-down approach.
Study Design: Retrospective case series.
Setting: Tertiary referral center.
Methods: This study analyzed records of 26 adult patients diagnosed with scalp cancer that spread to the calvarial region. Data collected included demographics, medical history, adjuvant therapy details, imaging, surgical outcomes, and postoperative oncological results.
Results: 26 patients with cancerous scalp lesions necessitating calvarial resection for deep margin control were identified in 22 men and 4 women. Mean age at diagnosis was 72.7 years. The most common histopathological diagnosis was Squamous cell carcinoma (n = 16). Partial removal of the calvarial lesions was achieved in all patients without any intraoperative complications. Twelve patients received adjuvant therapy consisting of the following modalities: radiation (6), chemotherapy (1), immunotherapy (1), a combination of immunotherapy and radiation (2), and a combination of chemotherapy and radiotherapy (2). There was a total of 7 recurrences: local (n = 3,11.5 %), regional (n = 3,11.5 %), distal (n = 1,3.8 %). Long term local control was achieved in (n = 23,88.4 %) of patients. The mean time of follow-up was 19.1 months, and the mean time to recurrence was 15.1 months.
Conclusion: Partial calvarial resection represents a viable, safe, and effective surgical technique for cancerous tissue removal, reducing risks associated with full thickness calvarial resection, and enhancing soft tissue healing when compared to the established gold standard.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.amjoto.2024.104456 | DOI Listing |
Zh Vopr Neirokhir Im N N Burdenko
August 2025
Burdenko Neurosurgical Center, Moscow, Russia.
Unlabelled: Malignant transformation of fibrous dysplasia in McCune-Albright syndrome is observed in less than 1% of cases, thus osteosarcoma is developing more frequently. According to the search in the PubMed database over the last 5 years, 13 publications were found, but none of them described cerebral cranium damage.
Material And Methods: A clinical observation of a 27-year-old patient with polyostotic fibrous dysplasia, skin manifestations and prolactin+HGH-secreting pituitary adenoma - McCune-Albright syndrome - without GNAS gene mutation is described.
Plast Reconstr Surg Glob Open
June 2025
Division of Pediatric Head and Neck Surgery, Department of Children's Surgery, AdventHealth for Children, Orlando, FL.
Langerhans cell histiocytosis is frequently characterized by lytic calvarial lesions, periodically necessitating cranioplasty in infant patients. Split calvarial bone graft cranioplasty is a feasible, though technically challenging option, which may be augmented with computer-assisted planning. Our case concerns a 14-month-old boy who presented with rapid evolution of soft calvarial masses of the subocciput.
View Article and Find Full Text PDFJ Neurosurg Case Lessons
June 2025
Departments of Neurosurgery, Renaissance School of Medicine at Stony Brook University, Stony Brook, New York.
Background: Supratentorial ependymoma, ZFTA fusion-positive, CNS WHO grade 3, is a rare pediatric brain tumor characterized by brisk mitotic activity and sometimes microvascular proliferation and/or necrosis. Typical treatment includes a combination of resection, chemotherapy, and radiation therapy. These tumors often present at age 3 or 4 years and have a poor prognosis.
View Article and Find Full Text PDFJ Craniofac Surg
June 2025
Division of Plastic Surgery, Department of Surgery, Mayo Clinic.
Surgical treatment and outcomes of fibrous dysplasia (FD) in pediatric patients are areas that have not been fully studied. The authors completed a retrospective review of 20 patients who had at least one surgery for craniofacial fibrous dysplasia before 18 years of age. Surgeries were categorized into 3 groups: bone contouring only; removal of the involved bone, contouring, and replacement of the contoured bone; or en bloc resection of the involved bone and reconstruction with an alloplastic material, bone allograft, or bone autograft obtained from non-involved sites.
View Article and Find Full Text PDFOral Maxillofac Surg Clin North Am
August 2025
Department of Neurosurgery, University Hospital Basel, Universitätsspital Basel, Neurochirurgie, Klinikum 1, Spitalstrasse 21, 4031 Basel, Switzerland.
Spheno-orbital (SOM) meningioma is a rare subtype of skull base tumor characterized by the proliferation of arachnoid cap cells with intradural expansion, hyperostosis of calvarial and spheno-orbital bone, and consecutive infiltration of critical surrounding neurovascular structures of the frontotemporal base of the skull. Surgical resection is often challenging due to the infiltrative growth and the anatomically complex localization. In most cases, a microsurgical transcranial approach is performed, resulting in the need to reconstruct the orbit with or without a cranioplasty.
View Article and Find Full Text PDF