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鞍区非功能性垂体腺瘤与脑膜瘤组成的碰撞瘤:1例报告及文献复习

Collision Tumor Composed of Nonfunctioning Pituitary Adenoma and Meningioma in the Sellar Region: Report of a Case and Literature Review.

作者信息

Baldawa Sachin, Raikhailkar Abhay

机构信息

Department of Neurosurgery, SS Baldawa Neurosciences and Women's Care Hospital, Solapur, Maharashtra, India.

Department of Pathology, SS Baldawa Neurosciences and Women's Care Hospital, Solapur, Maharashtra, India.

出版信息

Asian J Neurosurg. 2024 May 27;19(2):327-333. doi: 10.1055/s-0044-1787117. eCollection 2024 Jun.

Abstract

The coexistence of two histologically distinct neoplasms in the same area without histological admixture or an intermediate cell population zone represents a rare tumor type called collision tumor. Collision tumor of pituitary adenoma and meningioma has been reported years later following irradiation to pituitary adenoma. However, collision tumor of pituitary adenoma and meningioma in absence of irradiation therapy is extremely uncommon.  We report an unusual case of collision tumor involving diaphragma sella meningioma and pituitary adenoma in a 50-year-old lady without prior radiation therapy. She presented with visual blurring and impaired field of vision. Her preoperative magnetic resonance imaging (MRI) was suggestive of pituitary adenoma. Total excision of the lesion was performed through endoscopic transsphenoidal route. Histological diagnosis was consistent with collision tumor of pituitary adenoma and meningioma.  Collision tumor comprising of nonfunctioning pituitary adenoma and meningioma is extremely rare. Preoperative MRI may not always be able to distinguish these histologically distinct neoplasms. Hence, histopathological examination is necessary to establish the diagnosis. Endoscopic transsphenoidal approach may suffice in excision of these collision tumors. Close follow-up is necessary to detect tumor recurrence. Though the association of these tumors can be coincidental, casual relationship between the occurrence of collision tumors cannot be totally excluded.

摘要

同一区域内存在两种组织学上不同的肿瘤,且无组织学混合或中间细胞群区域,这代表一种罕见的肿瘤类型,称为碰撞瘤。垂体腺瘤和脑膜瘤的碰撞瘤在垂体腺瘤放疗多年后已有报道。然而,在未接受放疗的情况下,垂体腺瘤和脑膜瘤的碰撞瘤极为罕见。 我们报告一例罕见的碰撞瘤病例,该病例发生在一位50岁未接受过放疗的女性身上,涉及鞍膈脑膜瘤和垂体腺瘤。她表现为视力模糊和视野受损。术前磁共振成像(MRI)提示垂体腺瘤。通过内镜经蝶窦途径对病变进行了全切除。组织学诊断与垂体腺瘤和脑膜瘤的碰撞瘤一致。 由无功能性垂体腺瘤和脑膜瘤组成的碰撞瘤极为罕见。术前MRI可能并不总能区分这些组织学上不同的肿瘤。因此,需要进行组织病理学检查以明确诊断。内镜经蝶窦入路可能足以切除这些碰撞瘤。需要密切随访以检测肿瘤复发。尽管这些肿瘤的关联可能是偶然的,但不能完全排除碰撞瘤发生之间的因果关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/877a/11226278/d74a51497b3b/10-1055-s-0044-1787117-i23120015-1.jpg

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