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中枢神经系统钙化假性肿瘤累及颅底后部:病例报告及文献复习。

Calcifying Pseudoneoplasm of the Neuraxis Involving the Posterior Skull Base: A Case Report and Literature Review.

机构信息

University of Texas Health San Antonio, TX, USA.

出版信息

Int J Surg Pathol. 2021 Oct;29(7):733-739. doi: 10.1177/1066896921988935. Epub 2021 Jan 19.

Abstract

Calcifying pseudoneoplasm of the neuraxis is an uncommon, nonneoplastic fibro-osseous lesion of the central nervous system. At the time of this report, at least 150 cases have been reported in the literature. Because of the rarity of this lesion, it is often diagnostically challenging for radiologists and pathologists alike. In this article, we present a case of a 44-year-old woman with a 5.8-cm intracranial/skull base calcifying pseudoneoplasm of the neuraxis that was concerning for osteosarcoma on initial frozen section. Permanent sections revealed bone and fibrous stroma, calcifications, and nests of histiocytes with granuloma formation. Scattered, focally dense inflammatory foci and spindled cells outlining abundant large nodules of chondromyxoid matrix were also present. In this case report, we also reviewed recent literature for clinical presentations, radiologic findings, and histologic differential diagnoses. Familiarity with this lesion is important to avoid misdiagnosis leading to unnecessary and potentially harmful treatment.

摘要

中枢神经系统的钙化假性肿瘤是一种罕见的、非肿瘤性的中枢神经系统纤维骨性病变。在本报告之时,文献中至少已经报道了 150 例这种病变。由于这种病变非常罕见,放射科医生和病理科医生在诊断时都面临着挑战。在本文中,我们报告了一例 44 岁女性,颅内/颅底有一个 5.8 厘米的中枢神经系统钙化假性肿瘤,初步冷冻切片检查结果提示骨肉瘤。石蜡切片显示有骨和纤维基质、钙化以及组织细胞巢和肉芽肿形成。还存在散在的、局灶性密集的炎症灶和梭形细胞,围绕着大量软骨黏液样基质的大结节。在本病例报告中,我们还回顾了最近的文献,包括临床表现、影像学表现和组织学鉴别诊断。熟悉这种病变对于避免误诊导致不必要的和潜在有害的治疗非常重要。

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