Pollack I F, Hurtt M, Pang D, Albright A L
Department of Neurosurgery, University of Pittsburgh Medical Center, Children's Hospital of Pittsburgh, PA 15213.
Cancer. 1994 Jun 1;73(11):2869-78. doi: 10.1002/1097-0142(19940601)73:11<2869::aid-cncr2820731134>3.0.co;2-i.
The authors report three cases of histologically benign intracranial astrocytomas that developed in children and disseminated within the neuraxis. Multicentric disease was evident at the time of diagnosis in two of these patients, one of whom subsequently developed peritoneal seeding of tumor after placement of a ventriculoperitoneal shunt. To our knowledge, this latter represents the first documented case of extraneural seeding of a benign astrocytoma. All three children are currently alive and well 17-117 months after the diagnosis of tumor dissemination. We review the literature regarding this uncommon problem and discuss the pathophysiology and treatment options. Our results indicate that the presence of disseminated disease may not preclude long term survival, provided the lesions are truly benign histologically and that adjuvant therapy is instituted promptly.
作者报告了3例组织学上为良性的颅内星形细胞瘤病例,这些肿瘤发生于儿童,并在神经轴内播散。其中2例患者在诊断时即有明显的多中心病变,其中1例在置入脑室腹腔分流管后出现肿瘤的腹膜种植。据我们所知,后者是良性星形细胞瘤神经外种植的首例有记录病例。所有3例患儿在肿瘤播散诊断后17 - 117个月均存活且情况良好。我们回顾了关于这个罕见问题的文献,并讨论了病理生理学和治疗选择。我们的结果表明,只要病变在组织学上是真正良性的,并且及时进行辅助治疗,播散性疾病的存在可能并不妨碍长期生存。