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酷似矢状窦旁脑膜瘤的额顶叶原发性骨肉瘤:一例报告

Frontoparietal primary osteosarcoma mimicking parasagittal meningioma: A case report.

作者信息

Pokhrel Milan, Dhenga Sonam, Rauniyar Simran, Ali Abid, Buha Nirav Kumar, Gaire Roshan

机构信息

Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.

Maharajgunj Medical Campus, Institute of Medicine, Tribhuvan University, Kathmandu, Nepal.

出版信息

Int J Surg Case Rep. 2025 Sep;134:111724. doi: 10.1016/j.ijscr.2025.111724. Epub 2025 Jul 23.

Abstract

INTRODUCTION

Although Osteosarcoma is the most common primary malignant bone tumor, it rarely occurs in the craniofacial region. The incidence of primary craniofacial osteosarcoma is 0.33 to 0.41 per million.

CASE PRESENTATION

A 44-year-old male presented with a mass over the head for 5 months, blurring of vision for 1 month, and weakness of the left lower limb for 1 month. On physical examination, a mass of 10∗10 cm over the frontal region of the head with normal overlying skin without any tenderness. CT and MRI scans showed a mass centered around the midline cranium with both intracranial and extracranial components, with perilesional edema in adjacent brain tissue, with mass effect. Subtotal excision of the tumor was performed, and the patient was referred to another centre for radiotherapy and chemotherapy.

CLINICAL DISCUSSION

Osteosarcoma, being rare in the skull region, can often be confused with a much more common condition like meningioma. Osteosarcoma may resemble meningioma clinically and radiologically, particularly when meningioma has an extensive intraosseous component, either due to primary intraosseous origin or secondary bony invasion. Histopathology is the key to differentiating the two conditions. Surgery, along with radiotherapy and chemotherapy, is the key to management.

CONCLUSION

Osteosarcoma is a rare but important differential diagnosis in patients presenting with skull masses.

摘要

引言

骨肉瘤是最常见的原发性恶性骨肿瘤,但很少发生于颅面部区域。原发性颅面部骨肉瘤的发病率为百万分之0.33至0.41。

病例介绍

一名44岁男性,头部肿物5个月,视力模糊1个月,左下肢无力1个月。体格检查发现头部额部有一10×10厘米的肿物,其上覆盖皮肤正常,无压痛。CT和MRI扫描显示肿物以颅中线为中心,有颅内和颅外成分,相邻脑组织有瘤周水肿及占位效应。行肿瘤次全切除,患者被转至另一中心接受放疗和化疗。

临床讨论

骨肉瘤在颅骨区域罕见,常易与更常见的疾病如脑膜瘤相混淆。骨肉瘤在临床和影像学上可能类似脑膜瘤,尤其是当脑膜瘤有广泛的骨内成分时,这可能是由于原发性骨内起源或继发性骨侵犯。组织病理学是区分这两种疾病的关键。手术联合放疗和化疗是治疗的关键。

结论

骨肉瘤在出现颅骨肿物的患者中是一种罕见但重要的鉴别诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/12309478/368187cab778/gr1.jpg

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