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松果体区良、恶性肿瘤。

Benign and Malignant Tumors of the Pineal Region.

机构信息

Department of Neurological Surgery, Columbia University, New York, USA.

Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY, 10032, USA.

出版信息

Adv Exp Med Biol. 2023;1405:153-173. doi: 10.1007/978-3-031-23705-8_6.


DOI:10.1007/978-3-031-23705-8_6
PMID:37452938
Abstract

Pineal region tumors fall into five broad categories: benign pineal region tumors, glial tumors, papillary tumors, pineal parenchymal tumors, and germ cell tumors. Genetic and transcriptional studies have identified key chromosomal alterations in germinomas (RUNDC3A, ASAH1, LPL) and in pineocytomas/pineoblastomas (DROSHA/DICER1, RB1). Pineal region tumors generally present with symptoms of hydrocephalus including nausea, vomiting, papilledema, and the classical Parinaud's triad of upgaze paralysis, convergence-retraction nystagmus, and light-near pupillary dissociation. Workup requires neuroimaging and tissue diagnosis via biopsy. In germinoma cases, diagnosis may be made based on serum or CSF studies for alpha-fetoprotein or beta-HCG making the preferred treatment radiosurgery, thereby preventing the need for unnecessary surgeries. Treatment generally involves three steps: CSF diversion in cases of hydrocephalus, biopsy through endoscopic or stereotactic methods, and open surgical resection. Multiple surgical approaches are possible for approach to the pineal region. The original approach to the pineal region was the interhemispheric transcallosal first described by Dandy. The most common approach is the supracerebellar infratentorial approach as it utilizes a natural anatomic corridor for access to the pineal region. The paramedian or lateral supracerebellar infratentorial approach is another improvement that uses a similar anatomic corridor but allows for preservation of midline bridging veins; this minimizes the chance for brainstem or cerebellar venous infarction. Determination of the optimal approach relies on tumor characteristics, namely location of deep venous structures to the tumor along with the lateral eccentricity of the tumor. The immediate post-operative period is important as hemorrhage or swelling can cause obstructive hydrocephalus and lead to rapid deterioration. Adjuvant therapy, whether chemotherapy or radiation, is based on tumor pathology. Improvements within pineal surgery will require improved technology for access to the pineal region along with targeted therapies that can effectively treat and prevent recurrence of malignant pineal region tumors.

摘要

松果体区域肿瘤分为五类:良性松果体区域肿瘤、神经胶质瘤、乳头状肿瘤、松果体实质肿瘤和生殖细胞肿瘤。遗传和转录研究已经确定了生殖细胞瘤(RUNDC3A、ASAH1、LPL)和松果体细胞瘤/成松果体细胞瘤(DROSHA/DICER1、RB1)中的关键染色体改变。松果体区域肿瘤通常表现为脑积水的症状,包括恶心、呕吐、视乳头水肿和经典的 Parinaud 三联征,即上视麻痹、会聚性退缩性眼球震颤和光近瞳孔分离。检查需要神经影像学和通过活检进行组织诊断。在生殖细胞瘤的情况下,可能根据血清或 CSF 研究中的甲胎蛋白或β-HCG 进行诊断,从而使放射外科成为首选治疗方法,从而避免了不必要的手术。治疗通常包括三个步骤:脑积水患者行 CSF 引流、经内镜或立体定向方法进行活检以及开放性手术切除。松果体区域有多种手术入路。松果体区域的原始入路是 Dandy 首次描述的半球间经胼胝体入路。最常见的方法是小脑上后下开颅术,因为它利用了一个自然的解剖通道来进入松果体区域。旁正中或外侧小脑上后下开颅术是另一种改进方法,它使用了类似的解剖通道,但可以保留中线桥静脉;这最大限度地减少了脑干或小脑静脉梗死的机会。最佳入路的确定取决于肿瘤的特征,即肿瘤与深静脉结构的位置以及肿瘤的外侧偏心度。术后即刻非常重要,因为出血或肿胀可能导致梗阻性脑积水并导致迅速恶化。辅助治疗,无论是化疗还是放疗,都基于肿瘤病理学。松果体手术的改进需要改进进入松果体区域的技术以及可以有效治疗和预防恶性松果体区域肿瘤复发的靶向治疗。

相似文献

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Benign and Malignant Tumors of the Pineal Region.

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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
[Surgical approaches to pineal region - review article].

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引用本文的文献

[1]
Pineal Region Angiolipoma Resection by Supracerebellar Infratentorial Endoscopic Approach: A Case Study.

Am J Case Rep. 2025-3-21

[2]
Solitary fibrous tumor in the pineal region: A series of 5 cases and literature review.

J Neuropathol Exp Neurol. 2025-5-1

[3]
Pineal cyst in bipolar patient with normolithiaemia and positive fibromyalgic tender points.

Radiol Case Rep. 2024-12-12

本文引用的文献

[1]
In Reply: Mini-Pterional Craniotomy and Extradural Clinoidectomy for Clinoid Meningioma: Optimization of Exposure Using Augmented Reality Template: 2-Dimensional Operative Video.

Oper Neurosurg. 2020-12-15

[2]
Treatment outcome and long-term follow-up of central nervous system germ cell tumor using upfront chemotherapy with subsequent photon or proton radiation therapy: a single tertiary center experience of 127 patients.

BMC Cancer. 2020-10-9

[3]
Induction Chemotherapy Reduces Radiation Therapy Dose and Volume in the Treatment of Intracranial Germinoma: Results of the SMC-G13 Trial.

Int J Radiat Oncol Biol Phys. 2020-11-1

[4]
Optimization of Intracranial Germinoma Treatment: Radiotherapy Alone with Reduced Volume and Dose.

Int J Radiat Oncol Biol Phys. 2020-11-1

[5]
Papillary tumor in pineal region: Immunohistochemistry meeting the diagnostic challenge.

Indian J Pathol Microbiol. 2020

[6]
Pineoblastoma segregates into molecular sub-groups with distinct clinico-pathologic features: a Rare Brain Tumor Consortium registry study.

Acta Neuropathol. 2020-2

[7]
CBTRUS Statistical Report: Primary Brain and Other Central Nervous System Tumors Diagnosed in the United States in 2012-2016.

Neuro Oncol. 2019-11-1

[8]
CD24 and PRAME Are Novel Grading and Prognostic Indicators for Pineal Parenchymal Tumors of Intermediate Differentiation.

Am J Surg Pathol. 2020-1

[9]
Upfront chemotherapy followed by response adaptive radiotherapy for intracranial germinoma: Prospective multicenter cohort study.

Radiother Oncol. 2019-7-15

[10]
Pineal Region Gliomas: A Single-Center Experience with 25 Cases.

World Neurosurg. 2019-7-5

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