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下颌骨间叶性软骨肉瘤:一大难题——1例罕见的下颌骨间叶性软骨肉瘤病例报告及诊断与治疗难题讨论

Mesenchymal Chondrosarcoma of the Mandible, a Big Dilemma: Report of a Rare Case in Mesenchymal Chondrosarcoma of the Mandible-Report of a Case With Discussion of Diagnostic and Therapeutic Dilemmas.

作者信息

Karimi Abbas, Derakhshan Samira, Mosavat Farzaneh, Gholamhoseini Zahra, Khiavi Monir Moradzadeh

机构信息

Oral and Maxillofacial Surgery Department, Craniomaxillofacial Research Center, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.

Oral and Maxillofacial Pathology Department, School of Dentistry, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Case Rep Dent. 2024 Oct 28;2024:8884697. doi: 10.1155/2024/8884697. eCollection 2024.

Abstract

Chondrosarcomas are a group of malignant neoplasms with cartilaginous matrix production mostly found in flat and peripheral long bones. Mesenchymal chondrosarcoma is one of the most unusual and rare histological variants of chondrosarcoma, with a distinct histopathological appearance and biologically aggressive behavior. The amount of cartilage in mesenchymal chondrosarcoma may be so abundant that it is easily found in random sections or so scarce that numerous sections are required to discover it. In such cases, it is tough to make an accurate diagnosis, which leads to a big dilemma for pathologists and surgeons regarding diagnosis and treatment. Here, we report a mandibular mesenchymal chondrosarcoma in a 38-year-old male with a diagnosis of malignant small round cell tumor in incisional biopsy without any bone or chondroid formation. After ruling out lymphoma, a complete lesion excision was done. Diagnosis of mesenchymal chondrosarcoma was confirmed with small foci of chondroid material and strong positivity of tumoral cells for CD99 and S100. We highlight the fact that incisional biopsy frequently fails to provide sufficient tissue to establish the diagnosis of mesenchymal chondrosarcoma. Adequate tissue with multiple sections, detailed histopathological examination, and adjunctive IHC study are the keys to a definitive diagnosis.

摘要

软骨肉瘤是一组产生软骨基质的恶性肿瘤,多见于扁平骨和四肢长骨的外周。间叶性软骨肉瘤是软骨肉瘤中最不常见且罕见的组织学变体之一,具有独特的组织病理学表现和生物学侵袭性行为。间叶性软骨肉瘤中的软骨量可能很多,以至于在随机切片中很容易发现,也可能很少,以至于需要多张切片才能找到。在这种情况下,很难做出准确诊断,这给病理学家和外科医生在诊断和治疗方面带来了很大的困境。在此,我们报告一例38岁男性下颌骨间叶性软骨肉瘤,其切开活检诊断为恶性小圆形细胞肿瘤,未见任何骨或软骨样形成。排除淋巴瘤后,进行了完整病变切除。通过软骨样物质小灶以及肿瘤细胞对CD99和S100呈强阳性,确诊为间叶性软骨肉瘤。我们强调切开活检常常无法提供足够组织来确诊间叶性软骨肉瘤这一事实。足够的多切片组织、详细的组织病理学检查以及辅助免疫组化研究是明确诊断的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca8a/11535178/092f4376a197/CRID2024-8884697.001.jpg

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