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[Radiation-induced parotid leiomyosarcoma].
Ann Pathol
May 2024
Service d'anatomie et cytologie pathologiques, Inserm UMR 1253 I-brain, CHRU de Tours, université François-Rabelais de Tours, 2, boulevard Tonnellé, 37044 Tours, France; Faculté de médecine de Tours, université François-Rabelais de Tours, CHRU de Tours, 2, boulevard Tonnellé, 37044 Tours, France; House Institute Foundation, Los Angeles, CA 90057, États-Unis.
Introduction: First case of radiation-induced parotid leiomyosarcoma.
Anatomo-clinical Observation: A 50-year-old woman with a history of cervical irradiation for Hodgkin's lymphoma presented with a right parotid tumefaction. Examination noted a deep adherent pretragal mass with peripheral facial palsy.
Management of head & neck sarcomas in adults: A retrospective study.
J Craniomaxillofac Surg
August 2024
Plastic and Reconstructive Surgery Department, Athens General Anticancer - Oncology Hospital "Aghios Savvas", 171 Alexandras Ave, 11522, Athens, Greece. Electronic address:
The research purpose is to review the surgical approach and evaluate the results in adult patients with head and neck sarcomas. The histopathology varied, including two leiomyosarcomas, six malignant fibrous histiocytomas, two malignant peripheral nerve sheath tumors, four dermatofibrosarcomas protuberans, three osteosarcomas, two angiosarcomas, one liposarcoma, one Ewing sarcoma, one synovial sarcoma, two unclassified/non-differentiated sarcomas and one solitary fibrous tumor. Surgical resection included maxillectomy, mandibulectomy, craniectomy, parotidectomy, scalp resection, face skin resection and laminectomy.
View Article and Find Full Text PDFPrimary leiomyosarcoma of the parotid gland: Aspiration cytology with emphasis on differential diagnosis.
Cytopathology
November 2023
Department of Nuclear Medicine, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Most salivary gland neoplasms are of epithelial origin. Sarcomas of the parotid gland, including leiomyosarcoma, are exceedingly rare mesenchymal tumours. A definitive diagnosis of leiomyosarcoma is challenging on cytomorphology alone.
View Article and Find Full Text PDF[A case report of adult primary soft tissue sarcoma of the head and neck].
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi
February 2023
Head and neck primary soft tissue sarcoma is a rare adult connective tissue malignant tumor derived from mesenchymal tissue, which can occur in the paranasal sinuses, throat or neck space.The clinical manifestations are local spread masses in the head and neck or difficulty breathing, swallowing, etc al. MRI and enhanced CT examination are the most commonly used to diagnose such diseases.
View Article and Find Full Text PDFBirt-Hogg-Dubé Syndrome and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome: An Effective Multidisciplinary Approach to Hereditary Renal Cancer Predisposing Syndromes.
Front Oncol
September 2021
Faculty of Medicine, The University of Queensland, Herston, QLD, Australia.
Aim: We aimed to describe and analyse clinical features, characteristics, and adherence to surveillance guidelines in an Australian Birt-Hogg-Dubé syndrome (BHD) and hereditary leiomyomatosis and renal cell cancer (HLRCC) cohort.
Methods: All identified patients with a diagnosis of BHD or HLRCC at RBWH 01/01/2014-01/09/2019 were included (HREC/17/QRBW/276). All patients were initially assessed and counselled by a clinical geneticist and then referred to an adult nephrologist.
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