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颅骨淋巴瘤——一例病例报告及有助于鉴别诊断的特征

Cranial vault lymphoma - A case report and characteristics contributing to a differential diagnosis.

作者信息

Aoyama Satoshi, Nitta Naoki, Moritani Suzuko, Tsuji Atsushi

机构信息

Department of Neurosurgery, Shiga University of Medical Science, Otsu, Japan.

Department of Clinical Laboratory Medicine, Division of Diagnostic Pathology, Shiga University of Medical Science, Otsu, Japan.

出版信息

Surg Neurol Int. 2023 Mar 24;14:107. doi: 10.25259/SNI_1040_2022. eCollection 2023.

Abstract

BACKGROUND

Lymphomas of the cranial vault are rare and are often misdiagnosed preoperatively as presumptive meningioma with extracranial extension.

CASE DESCRIPTION

A 58-year-old woman was referred and admitted to our department with a rapidly growing subcutaneous mass over the right frontal forehead of 2 months' duration. The mass was approximately 13 cm at its greatest diameter, elevated 3 cm above the contour of the peripheral scalp, and attached to the skull. Neurological examination showed no abnormalities. Skull X-rays and computed tomography showed preserved original skull contour despite the large extra and intracranial tumor components sandwiching the cranial vault. Digital subtraction angiography showed a partial tumor stain with a large avascular area. Our preoperative diagnostic hypothesis was meningioma. We performed a biopsy and histological findings were characteristic of a diffuse large B-cell lymphoma. A very high preoperative level of soluble interleukin-2 receptor (5390 U/mL; received postoperatively) also suggested lymphoma. The patient received chemotherapy but died of disease progression 10 months after the biopsy.

CONCLUSION

Several preoperative features of the present case are clues to the correct diagnostic hypothesis of cranial vault diffuse large B-cell lymphoma rather than meningioma, including a rapidly growing subcutaneous scalp mass, poor vascularization, and limited skull destruction relative to the size of the soft-tissue mass.

摘要

背景

颅骨淋巴瘤罕见,术前常被误诊为伴有颅外扩展的推测性脑膜瘤。

病例描述

一名58岁女性因右侧额部皮下肿物迅速增大2个月前来就诊并入住我科。肿物最大直径约13 cm,高出周边头皮轮廓3 cm,与颅骨相连。神经系统检查无异常。颅骨X线和计算机断层扫描显示,尽管颅内外有巨大肿瘤成分夹在颅骨穹窿之间,但颅骨原始轮廓仍保留。数字减影血管造影显示部分肿瘤染色,有大片无血管区。我们术前的诊断假设是脑膜瘤。我们进行了活检,组织学检查结果为弥漫性大B细胞淋巴瘤特征性表现。术前可溶性白细胞介素-2受体水平非常高(5390 U/mL;术后测得)也提示为淋巴瘤。患者接受了化疗,但活检后10个月因疾病进展死亡。

结论

本病例的几个术前特征提示颅骨弥漫性大B细胞淋巴瘤而非脑膜瘤的正确诊断假设,包括迅速增大的头皮皮下肿物、血管化差以及相对于软组织肿物大小而言有限的颅骨破坏。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fcc/10070291/abfac0dda200/SNI-14-107-g001.jpg

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