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部分切除术后四十年,起源于桥小脑角表皮样囊肿残余的颅内鳞状细胞癌

Intracranial Squamous Cell Carcinoma Arising From a Cerebellopontine Angle Epidermoid Cyst Remnant Four Decades After Partial Resection.

作者信息

Cuoco Joshua A, Rogers Cara M, Busch Christopher M, Apfel Lisa S, Entwistle John J, Marvin Eric A

机构信息

Section of Neurosurgery, Carilion Clinic, Roanoke, VA, United States.

Virginia Tech Carilion School of Medicine, Roanoke, VA, United States.

出版信息

Front Oncol. 2019 Jul 30;9:694. doi: 10.3389/fonc.2019.00694. eCollection 2019.

DOI:10.3389/fonc.2019.00694
PMID:31428577
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6689955/
Abstract

Intracranial epidermoid cysts are benign lesions that typically remain asymptomatic; however, although histopathologically benign, these cysts can rarely undergo malignant transformation into squamous cell carcinoma. Primary intracranial squamous cell carcinoma carries a poor prognosis as optimal treatment modalities remain unclear due to their low incidence. Here, we present a case of a cerebellopontine angle epidermoid cyst remnant that underwent malignant transformation into squamous cell carcinoma 40 years after partial resection. To our knowledge, this case establishes the longest time interval to date for an intracranial epidermoid cyst to undergo malignant transformation. We also review the relevant literature and discuss recent retrospective clinical studies that have analyzed the effect of multimodal treatment approaches on survival outcomes in patients with these lesions.

摘要

颅内表皮样囊肿是良性病变,通常无症状;然而,尽管这些囊肿在组织病理学上是良性的,但很少会恶变为鳞状细胞癌。原发性颅内鳞状细胞癌预后较差,由于其发病率低,最佳治疗方式仍不明确。在此,我们报告一例桥小脑角表皮样囊肿残余物在部分切除40年后恶变为鳞状细胞癌的病例。据我们所知,该病例是迄今为止颅内表皮样囊肿发生恶变时间间隔最长的。我们还回顾了相关文献,并讨论了最近的回顾性临床研究,这些研究分析了多模式治疗方法对这些病变患者生存结果的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e23/6689955/8f1b092d8259/fonc-09-00694-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e23/6689955/3f1a9ba0596d/fonc-09-00694-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e23/6689955/8f1b092d8259/fonc-09-00694-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e23/6689955/3f1a9ba0596d/fonc-09-00694-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2e23/6689955/8f1b092d8259/fonc-09-00694-g0002.jpg

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Meckel Cave Epidermoid Cyst Presenting as Multiple Cranial Nerve Deficits Due to Indirect Tumoral Compression of the Cavernous Sinus: A Case Report and Literature Review.因海绵窦间接肿瘤压迫导致多发颅神经功能缺损的梅克尔腔表皮样囊肿:一例报告及文献综述
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Cancers (Basel). 2024 Oct 15;16(20):3487. doi: 10.3390/cancers16203487.
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