Cannon T C, Bane B L, Kistler D, Schoenhals G W, Hahn M, Leech R W, Brumback R A
Pathology Department, The University of Oklahoma Health Sciences Center and VA Medical Center, Oklahoma City 73104, USA.
Arch Pathol Lab Med. 1998 Aug;122(8):737-9.
The authors report a case of a primary extraskeletal osteosarcoma arising within an epidermoid cyst in the parenchyma of the cerebellum in a 64-year-old woman. On initial presentation, the tumor involved the midline cerebellum without attachment to the surrounding dura mater or calvarium. Complete medical and radiologic evaluation failed to reveal a primary skeletal or other extraskeletal osteosarcoma. To our knowledge, this is the first reported case of a primary extraskeletal osteosarcoma within the cerebellum. Osteosarcoma as a primary brain tumor is exceedingly rare, and only three cases (all occurring within the cerebral hemispheres) have been reported previously. The histogenesis of primary sarcomas of the brain is not evident. The associated finding of an epidermoid cyst suggests the tumor originated from a teratoma.
作者报告了一例64岁女性小脑实质内表皮样囊肿内发生的原发性骨外骨肉瘤病例。初次就诊时,肿瘤累及小脑中线,未附着于周围硬脑膜或颅骨。全面的医学和影像学评估未能发现原发性骨或其他骨外骨肉瘤。据我们所知,这是首次报道的小脑内原发性骨外骨肉瘤病例。骨肉瘤作为原发性脑肿瘤极为罕见,此前仅报道过3例(均发生在大脑半球)。脑原发性肉瘤的组织发生尚不明确。表皮样囊肿这一相关发现提示肿瘤起源于畸胎瘤。