Mosalleum Esraa, Afrogheh Amir, Stofberg Sacha, Bezuidenhout Abraham Fourie, Schneider Johann, Hille Jos
Department of Oral & Maxillofacial Pathology, NHLS, Tygerberg Hospital Laboratories, Faculty of Dentistry, University of the Western Cape, Cape Town, South Africa,
Head Neck Pathol. 2015 Mar;9(1):158-64. doi: 10.1007/s12105-014-0550-8. Epub 2014 Jun 20.
Sarcomas of the larynx are exceedingly uncommon, of which primary laryngeal osteosarcomas are the rarest. To date, 25 cases of primary laryngeal osteosarcomas have been reported in the literature. Laryngeal osteosarcomas may closely simulate sarcomatoid carcinomas, since both entities share clinical, histological and immunohistochemical features. Herein, we report a case of primary laryngeal osteosarcoma in a 55 year old male, focusing on the importance of light microscopic, immunohistochemical and ultrastructural features in accurately establishing the diagnosis. In addition, the current paper provides a review of the English language literature on the subject. Laryngeal osteosarcomas usually carry a dismal prognosis with no general consensus on the most effective mode of therapy. Similarly, the current patient developed bilateral lung metastases 8 months after the initial surgery.
喉肉瘤极为罕见,其中原发性喉骨肉瘤最为罕见。迄今为止,文献中已报道25例原发性喉骨肉瘤。喉骨肉瘤可能与肉瘤样癌极为相似,因为这两种实体在临床、组织学和免疫组化特征上有共同之处。在此,我们报告一例55岁男性原发性喉骨肉瘤病例,重点阐述光学显微镜、免疫组化和超微结构特征在准确诊断中的重要性。此外,本文还对该主题的英文文献进行了综述。喉骨肉瘤通常预后不佳,对于最有效的治疗方式尚无普遍共识。同样,该患者在初次手术后8个月出现双侧肺转移。