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颅底恶性颗粒细胞瘤。

Malignant granular cell tumor of the skull base.

作者信息

Meling T R, Fridrich K, Evensen J F, Nedregaard B

机构信息

Department of Neurosurgery, Rikshospitalet-Radiumhospitalet University Hospital, Oslo, Norway.

出版信息

Skull Base. 2008 Jan;18(1):59-66. doi: 10.1055/s-2007-992763.

Abstract

OBJECTIVE AND IMPORTANCE

Malignant granular cell tumors (MGCTs) are extremely rare, high-grade sarcomas of Schwann cell origin. They often metastasize and are associated with short survival. We describe a patient with a large MGCT arising from the suboccipital nerve that eroded the posterior skull base, invaded the perifocal neck muscles, demonstrated perineural extension, and metastasized to regional lymph nodes.

CLINICAL PRESENTATION

A 60-year-old woman with several years' history of neck pain noticed a right-sided suboccipital swelling 4 months prior to seeking medical attention. Magnetic resonance imaging (MRI) showed a 5-cm bone-eroding suboccipital tumor and a second tumor, anterocaudal to this, 4 cm in diameter.

INTERVENTION

The patient underwent surgery. A 4-cm multinodular tumor was removed, freeing it from the internal jugular vein. A 5-cm suboccipital tumor infiltrated the trapezius, semispinalis capitis, and longissimus capitis muscles. The major and minor rectus capitis muscles were completely engulfed by tumor and their attachments to the occipital bone completely eroded. The oblique capitis muscle was infiltrated at its attachment to the C1 transverse process. These muscles were resected with a free margin to remove all tumor tissue. We then removed tumor encasing the right vertebral artery, the medial mastoid process up to the transverse sinus and anteriorly to the stylomastoid foramen, and lastly, the posterior third of the occipital condyle, achieving a gross total removal and no visible residual on postoperative contrast-enhanced MRI.

CONCLUSION

This case represents the first report of resected primary MGCT involving the posterior fossa and arising from the suboccipital nerve.

摘要

目的及重要性

恶性颗粒细胞瘤(MGCTs)是极为罕见的源自施万细胞的高级别肉瘤。它们常发生转移且生存期短。我们描述了一名患者,其巨大的MGCT起源于枕下神经,侵蚀了后颅底,侵犯了病灶周围的颈部肌肉,出现神经周围浸润,并转移至区域淋巴结。

临床表现

一名有多年颈部疼痛病史的60岁女性,在就医前4个月注意到右侧枕下肿胀。磁共振成像(MRI)显示一个5厘米大小侵蚀骨质的枕下肿瘤,以及在其前尾侧一个直径4厘米的第二个肿瘤。

干预措施

患者接受了手术。切除了一个4厘米大小的多结节肿瘤,并将其与颈内静脉分离。一个5厘米大小的枕下肿瘤浸润了斜方肌、头半棘肌和头最长肌。头直肌的主要和次要部分完全被肿瘤包绕,它们与枕骨的附着点完全被侵蚀。头斜肌在其与C1横突的附着处被浸润。这些肌肉被切除,切缘阴性以去除所有肿瘤组织。然后我们切除了包裹右椎动脉的肿瘤、直至横窦的内侧乳突以及茎乳孔前方的部分,最后切除了枕髁的后三分之一,实现了肉眼下全切,术后对比增强MRI未见明显残留。

结论

本病例是首例关于切除的原发性MGCT累及后颅窝并起源于枕下神经的报道。

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