Department of Radiology (J.C.B., T.J.K., L.E., J.G.), Mayo Clinic, Rochester, Minnesota
Department of Laboratory Medicine and Pathology (J.T.-L.), Mayo Clinic, Rochester, Minnesota.
AJNR Am J Neuroradiol. 2021 Aug;42(8):1370-1374. doi: 10.3174/ajnr.A7136. Epub 2021 May 6.
Pilomyxoid astrocytoma is a rare form of pediatric CNS malignancy first classified in 2007 by the World Health Organization. The tumors are similar to pilocytic astrocytomas, sharing both some imaging and histologic traits. However, pilomyxoid astrocytomas portend a more ominous prognosis, with more aggressive local tendencies and a greater proclivity for leptomeningeal spread. Although tissue sampling is ultimately required to differentiate pilocytic astrocytomas and pilomyxoid astrocytomas, some imaging features can be used to suggest a pilomyxoid astrocytoma, including homogeneous enhancement, leptomeningeal seeding, and lack of intratumoral cysts. In this article, a case of a hypothalamic pilomyxoid astrocytoma is described, in which the presenting disorder was profound generalized lipodystrophy. The aforementioned imaging characteristics of pilomyxoid astrocytomas are reviewed, as are the pathologic features of such tumors, including their angiocentric cellular arrangement and myxoid background.
毛细胞黏液样星形细胞瘤是一种罕见的儿童中枢神经系统恶性肿瘤,于 2007 年由世界卫生组织首次分类。这些肿瘤与毛细胞星形细胞瘤相似,具有一些相似的影像学和组织学特征。然而,毛细胞黏液样星形细胞瘤预示着更凶险的预后,具有更具侵袭性的局部倾向和更高的向软脑膜播散的倾向。尽管最终需要组织取样来区分毛细胞星形细胞瘤和毛细胞黏液样星形细胞瘤,但一些影像学特征可用于提示毛细胞黏液样星形细胞瘤,包括均匀强化、软脑膜播散和肿瘤内无囊变。本文描述了一例下丘脑毛细胞黏液样星形细胞瘤,其表现为严重的全身性脂肪营养不良。本文回顾了毛细胞黏液样星形细胞瘤的上述影像学特征,以及这些肿瘤的病理特征,包括其血管中心性细胞排列和黏液样背景。