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下颌骨软骨母细胞性骨肉瘤:一例报告

Mandibular Chondroblastic Osteosarcoma: A Case Report.

作者信息

Hasen Yousef M, Tawel Hoda, Alreeshi Khoulah M, Khalifa Osama, Furjani Jamal M

机构信息

Department of Pathology, Faculty of Dentistry, University of Zawia, Zawia, LBY.

Department of Pathology, Faculty of Medicine, University of Zawia, Zawia, LBY.

出版信息

Cureus. 2024 Feb 6;16(2):e53713. doi: 10.7759/cureus.53713. eCollection 2024 Feb.

Abstract

Osteosarcoma is primarily a long-bone disease that rarely affects the facial bones. Chondroblastic osteosarcoma is a subvariant of osteosarcoma. Its defining characteristics include the presence of malignant spindle and polygonal cells, as well as a thick layer of chondroid matrix and interwoven neoplastic tissue deposition. Mandibular chondroblastic osteosarcoma, in particular, is often overlooked and disregarded as a presumptive diagnosis at the time of initial presentation. This is mainly because of its rarity or inadequate lesion evaluation. Here, we present the case of a 47-year-old female patient with a rapidly growing swelling at the anterior mandible that was initially misdiagnosed as an ossifying fibroma of the mandible. The subsequent histopathological examination confirmed the diagnosis of chondroblastic osteosarcoma of the mandible. The patient requested a more extensive and aggressive excision, with the possibility of adjuvant radiation or chemotherapy. This article illustrates a rare case of mandibular chondroblastic osteosarcoma, with a focus on the clinical and pathological features of the tumor that should be taken into account when making a differential diagnosis for oral bone lesions.

摘要

骨肉瘤主要是一种长骨疾病,很少累及面骨。软骨母细胞性骨肉瘤是骨肉瘤的一个亚型。其特征性表现包括存在恶性梭形细胞和多角形细胞,以及一层厚厚的软骨样基质和交织的肿瘤组织沉积。特别是下颌骨软骨母细胞性骨肉瘤,在初次就诊时常常被忽视或误诊。这主要是因为其罕见性或对病变评估不足。在此,我们报告一例47岁女性患者,其下颌前部出现迅速增大的肿物,最初被误诊为下颌骨骨化性纤维瘤。随后的组织病理学检查确诊为下颌骨软骨母细胞性骨肉瘤。患者要求进行更广泛、积极的切除,并可能进行辅助放疗或化疗。本文阐述了一例罕见的下颌骨软骨母细胞性骨肉瘤病例,重点关注在对口腔骨病变进行鉴别诊断时应考虑的肿瘤临床和病理特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58aa/10919317/c4b3eb233037/cureus-0016-00000053713-i01.jpg

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