Huddleston Brent J, Sjostrom Christopher M, Collins Brian T
Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Acta Cytol. 2010 Sep-Oct;54(5 Suppl):958-62.
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare, aggressive tumor of the central nervous system. It is primarily seen in younger age-groups, and the cytomorphology has only been infrequently described.
We present a case of AT/RT arising in the cervical spine of a 6-month-old boy. The cerebrospinal fluid (CSF) cytology and correlating findings are described. The CSF cytomorphologic findings of the AT/RT cells are most notably large cells, eccentrically placed pleomorphic nuclei, prominent nucleoli and, commonly, cytoplasmic inclusions, as well as a second population of smaller mononuclear cells with minimal cytoplasm.
The cervical spine is a rare site for AT/RT to arise. It is important for pathologists to recognize the cytomorphologic features of AT/RT in the CSF of patients with this tumor to help determine prognosis and disease progression.
非典型畸胎样/横纹肌样瘤(AT/RT)是一种罕见的、侵袭性的中枢神经系统肿瘤。它主要见于较年轻的年龄组,其细胞形态学仅偶尔有描述。
我们报告一例发生于一名6个月大男婴颈椎的AT/RT病例。描述了脑脊液(CSF)细胞学及相关发现。AT/RT细胞的脑脊液细胞形态学发现最显著的是大细胞、偏心放置的多形性核、突出的核仁,并且通常有细胞质内含物,以及另一群细胞质极少的较小单核细胞。
颈椎是AT/RT罕见的发病部位。病理学家认识这种肿瘤患者脑脊液中AT/RT的细胞形态学特征对于帮助确定预后和疾病进展很重要。