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周皮细胞增多症与水肿形成:脑膜瘤的一种独特临床病理变体

Pericytosis and edema generation: a unique clinicopathological variant of meningioma.

作者信息

Robinson J C, Challa V R, Jones D S, Kelly D L

机构信息

Department of Neurosurgery, Wake Forest University, Bowman Gray School of Medicine, Winston-Salem, North Carolina, USA.

出版信息

Neurosurgery. 1996 Oct;39(4):700-6; discussion 706-7. doi: 10.1097/00006123-199610000-00009.

Abstract

OBJECTIVE

We report a group of eight patients with a distinctive histological variant of meningioma that is associated with severe peritumoral edema. The clinical presentation, radiographic findings, and histology of this type of tumor may lead to misdiagnosis as an aggressive or malignant process.

METHODS

We reviewed the histology from patients who had removal of meningiomas performed in our institution between 1978 and 1992. Tumors having abnormal proliferation of cells in the intramural vascular spaces were selected for study; case histories and radiographs were reviewed. Tumor material was subjected to special stains, immunocytochemical examination, and election microscopy.

RESULTS

Several lesions were misread radiographically as being malignant. Patients underwent craniotomy with complete excision of the tumor. All lesions were small (< or = 3 cm), and no brain invasion, unusual tumor vascularity, or dural sinus involvement was noted in any case. Histologically, the meningioma pattern in each case was meningothelial and benign in appearance. The immunocytochemical and electron microscopic features of the unusual cells in the blood vessel walls are most consistent with their being of pericytic origin. All patients have remained asymptomatic and without evidence of tumor recurrence with follow-up from 3 to 12 years.

CONCLUSION

These tumors showed proliferation of pericytes in blood vessel walls and represent a new subtype of meningothelial meningioma. The apparently benign nature of these lesions necessitates their recognition. Characteristic findings of pericytic proliferation associated with edema generation have led us to descriptively term this the PEG variant of meningioma.

摘要

目的

我们报告一组8例患有独特组织学变异型脑膜瘤的患者,该变异型与严重的瘤周水肿相关。这类肿瘤的临床表现、影像学表现及组织学特征可能导致被误诊为侵袭性或恶性病变。

方法

我们回顾了1978年至1992年间在我们机构接受脑膜瘤切除术患者的组织学情况。选择壁内血管间隙中细胞异常增殖的肿瘤进行研究;回顾病例史和影像学资料。对肿瘤组织进行特殊染色、免疫细胞化学检查及电子显微镜检查。

结果

数例病变在影像学上被误读为恶性。患者接受了开颅手术并完整切除肿瘤。所有病变均较小(≤3 cm),且在任何病例中均未发现脑侵犯、异常肿瘤血管或硬脑膜窦受累。组织学上,每例脑膜瘤的形态均为脑膜上皮型且外观良性。血管壁中异常细胞的免疫细胞化学和电子显微镜特征最符合其为周细胞起源。所有患者在3至12年的随访中均无症状且无肿瘤复发迹象。

结论

这些肿瘤显示血管壁周细胞增殖,代表脑膜上皮型脑膜瘤的一种新亚型。这些病变明显的良性性质需要予以识别。与水肿形成相关的周细胞增殖的特征性表现使我们将其描述性地命名为脑膜瘤的PEG变异型。

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