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一名儿童后颅窝室管膜瘤,伴有广泛的软骨-骨化生,发生于小脑脑桥角,伪装成前庭神经鞘瘤:一种极其罕见的临床病理表现并文献复习

Posterior Fossa Ependymoma in a Child with Extensive Chondro-Osseous Metaplasia Occurring at Cerebellopontine Angle and Masquerading as a Vestibular Schwannoma: An Exceptionally Rare Clinicopathological Manifestation with Review of Literature.

作者信息

Malik Shaivy, Samanta Siddhartha Sankar, Kolte Sachin

机构信息

Department of Pathology, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India.

出版信息

J Neurol Surg Rep. 2024 Aug 29;85(3):e132-e137. doi: 10.1055/a-2372-6701. eCollection 2024 Jul.

Abstract

Ependymoma occurring at the cerebellopontine (CP) angle is an extremely uncommon sight and poses diagnostic and management dilemmas to neurosurgeons, radiologists, and neuropathologists alike. Moreover, the presence of extensive chondro-osseous metaplastic elements in ependymomas is an exceptionally infrequent histopathological manifestation. However, due to the seldom-seen nature of this histomorphological feature, there is no definite consensus regarding its etiopathogenesis and clinical consequences, and there is an extreme scarcity of literature elucidating its clinicopathological spectrum and prognostic significance. Herein, we illustrate an intriguing clinical tale of a 7-year-old male child with posterior fossa ependymoma, central nervous system (CNS) World Health Organization (WHO) grade 3, arising at the right CP angle and masquerading as a vestibular schwannoma, which in itself is a rare presentation, and additionally, exhibiting extensive chondro-osseous metaplasia, which is a very uncommon histomorphological observation. To the best of the authors' knowledge and after a comprehensive literature search, the coexistence of these two rare observations has merely been described once in international literature. This case sheds light on and highlights the importance of keeping ependymoma as a possible differential while coming across CP angle space-occupying lesions. They should be diligently distinguished from schwannomas and other masqueraders that typically occur at this site, as they have diverse management and follow-up protocols, with varying prognostic outcomes for the patients. Moreover, this case also unravels and details the clinicopathological characteristics of a scarcely described feature of chondro-osseous metaplasia in ependymomas.

摘要

发生于小脑桥脑角(CP角)的室管膜瘤极为罕见,给神经外科医生、放射科医生和神经病理学家带来了诊断和治疗难题。此外,室管膜瘤中广泛存在软骨-骨化生成分是一种极其罕见的组织病理学表现。然而,由于这种组织形态学特征罕见,其发病机制和临床后果尚无明确共识,且阐明其临床病理谱和预后意义的文献极为匮乏。在此,我们讲述一个有趣的临床病例,一名7岁男童患有后颅窝室管膜瘤,世界卫生组织(WHO)中枢神经系统(CNS)3级,起源于右侧CP角,伪装成前庭神经鞘瘤,而前庭神经鞘瘤本身就是一种罕见的表现,此外,该肿瘤还表现出广泛的软骨-骨化生,这是一种非常罕见的组织形态学观察结果。据作者所知,经过全面的文献检索,国际文献中仅一次描述过这两种罕见情况的共存。该病例揭示并强调了在遇到CP角占位性病变时,将室管膜瘤作为可能的鉴别诊断的重要性。应仔细将它们与通常发生在该部位的神经鞘瘤和其他伪装病变区分开来,因为它们有不同的治疗和随访方案,患者的预后结果也各不相同。此外,该病例还揭示并详细描述了室管膜瘤中罕见的软骨-骨化生特征的临床病理特点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c39d/11361780/482e2fbc8e45/10-1055-a-2372-6701-i24may0020-1.jpg

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