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具有不同组织形态学模式的颌骨骨肉瘤:病例报告

Osteosarcoma of Jaw with Varying Histomorphologic Patterns: Case Report.

作者信息

Agrawal Ruchika Ravi, Bhavthankar Jyoti Dilip, Mandale Mandakini Subhash, Patil Purva Prakash

机构信息

Department of Oral Pathology, Government Dental College and Hospital, Aurangabad, Maharashtra, India.

出版信息

J Orthop Case Rep. 2017 Jan-Feb;7(1):61-64. doi: 10.13107/jocr.2250-0685.690.

DOI:10.13107/jocr.2250-0685.690
PMID:28630843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5458701/
Abstract

INTRODUCTION

Osteosarcoma is a malignant mesenchymal tumor whose cancerous cells produce osteoid matrix. It is a common primary malignant bone tumor, representing 23% of total head and neck malignancies. Osteosarcomas of the jaws are rare lesions, representing only 4-7% of all osteosarcomas. This presentation discusses the clinical, radiographical, and histopathological features of a case of osteosarcoma of the mandible with unusual histopathological appearance.

CASE REPORT

A 21-year-old male patient reported with a diffuse swelling of the right side of mandible with dull ache and increasing difficulties with eating and speech. Incisional biopsy done showed a histopathological picture of osteosarcoma and osteoblastoma. Hemimandibulectomy was done and the histopathology showed varying patterns of the lesion-like osteoblastoma-like osteosarcoma and osteoblastic variant of osteosarcoma. Focal areas in the lesion also showed fibrohistiocytic differentiation which may be mistaken for malignant fibrous histiocytoma. Hemangiopericytomatous appearance was also seen. Hence, it was necessary to differentiate between all the lesions as the treatment plan for all these lesions is different. Rarely, tumor may show a spectrum of histopathology as seen here in a case of osteosarcoma of the mandible.

CONCLUSION

The treatment plan and prognosis for each type of these lesions are different. Thus, thorough histopathological evaluation will help in accurate diagnosis, proper treatment planning, and prognosis of these lesions.

摘要

引言

骨肉瘤是一种恶性间充质肿瘤,其癌细胞可产生类骨质基质。它是一种常见的原发性恶性骨肿瘤,占头颈部恶性肿瘤总数的23%。颌骨骨肉瘤是罕见的病变,仅占所有骨肉瘤的4-7%。本文介绍一例具有不寻常组织病理学表现的下颌骨骨肉瘤的临床、影像学和组织病理学特征。

病例报告

一名21岁男性患者因下颌骨右侧弥漫性肿胀、隐痛以及进食和言语困难加重前来就诊。切开活检显示为骨肉瘤和成骨细胞瘤的组织病理学图像。行半侧下颌骨切除术,组织病理学显示病变呈现不同模式,如成骨细胞瘤样骨肉瘤和骨肉瘤的成骨细胞变体。病变中的局灶区域还显示纤维组织细胞分化,可能被误诊为恶性纤维组织细胞瘤。还可见血管外皮细胞瘤样表现。因此,由于所有这些病变的治疗方案不同,有必要对所有病变进行鉴别。罕见情况下,肿瘤可能呈现一系列组织病理学表现,如下颌骨骨肉瘤病例所示。

结论

这些病变各类型的治疗方案和预后不同。因此,全面的组织病理学评估将有助于对这些病变进行准确诊断、合理治疗规划和判断预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/edbca8e7a166/JOCR-7-61-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/1f79aeb94d6f/JOCR-7-61-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/9d7b4755d595/JOCR-7-61-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/edbca8e7a166/JOCR-7-61-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/1f79aeb94d6f/JOCR-7-61-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/9d7b4755d595/JOCR-7-61-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce2d/5458701/edbca8e7a166/JOCR-7-61-g003.jpg

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引用本文的文献

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Clin Case Rep. 2023 Apr 12;11(4):e7198. doi: 10.1002/ccr3.7198. eCollection 2023 Apr.

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Diaphyseal osteosarcoma with varying histomorphologic patterns.具有不同组织形态学模式的骨干骨肉瘤
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