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右侧耻骨支复发性骨外脑膜瘤的细胞形态学:一例报告及文献复习

Cytomorphology of Recurrent Osseous Extracranial Meningioma of Right Pubic Ramus:: Report of a Case and Literature Review.

作者信息

Bokhari Aqiba, Hibshoosh Hanina, Tiscornia-Wasserman Patricia G

机构信息

Division of Cytopathology, New York Presbyterian-Columbia University Medical Center, New York.

Department of Pathology and Cell Biology, New York Presbyterian-Columbia University Medical Center, New York.

出版信息

Diagn Cytopathol. 2016 Jul;44(7):618-22. doi: 10.1002/dc.23483. Epub 2016 Apr 15.

Abstract

Meningiomas are well-recognized neoplasms of the central nervous system. Primary extracranial meningiomas (ECMs) are extremely rare and arise in various anatomic sites. We present a 56-year-old female with 13-year history of primary grade I meningothelial meningioma of right pubic symphysis, orthotopic heart transplant, and right total hip arthroplasty, who presented with progressive right hip pain for 3 weeks. Primary intracranial, intraspinal and other tumors were excluded. Imaging revealed a destructive lytic lesion at right superior and inferior pubic rami and body, associated with extensive bone destruction and soft tissue mass. Touch imprint (TI) cytology of computed tomography (CT)-guided core biopsy from the right pubic ramus (PRA) lesion showed a spindle cell neoplasm, with classical syncytial, lobular, and whorling cellular arrangement, composed of spindle, oval or round nuclei with occasional pseudoinclusions, consistent with known history of osseous meningioma. Tumor was further characterized by histopathology as grade 1 meningioma with meningothelial features. To our knowledge, primary osseous ECM arising specifically at the PRA has not been reported previously. ECM at this site may pose a diagnostic challenge for cytologists as its features may resemble other more commonly observed lesions. Accurate diagnosis requires awareness of occurrence of ECM at PRA and recognition of its characteristic cytomorphology. TI cytological features of our case are presented and previously described cytology of ECMs and diagnostic pitfalls are reviewed. Diagn. Cytopathol. 2016;44:618-622. © 2016 Wiley Periodicals, Inc.

摘要

脑膜瘤是中枢神经系统中广为人知的肿瘤。原发性颅外脑膜瘤(ECM)极为罕见,可发生于各种解剖部位。我们报告了一名56岁女性,有13年右侧耻骨联合I级原发性脑膜皮型脑膜瘤病史,接受过原位心脏移植和右侧全髋关节置换术,她出现进行性右髋疼痛3周。排除了原发性颅内、脊髓及其他肿瘤。影像学检查显示右侧耻骨上下支及耻骨体有破坏性溶骨性病变,伴有广泛骨质破坏和软组织肿块。对右侧耻骨支(PRA)病变进行计算机断层扫描(CT)引导下的核心活检,其触摸印片(TI)细胞学检查显示为梭形细胞瘤,具有典型的合体细胞、小叶状和漩涡状细胞排列,由梭形、椭圆形或圆形核组成,偶尔可见假包涵体,与已知的骨脑膜瘤病史相符。肿瘤经组织病理学进一步特征化为具有脑膜皮特征的1级脑膜瘤。据我们所知,以前尚未报道过专门发生在PRA的原发性骨ECM。该部位的ECM可能给细胞病理学家带来诊断挑战,因为其特征可能类似于其他更常见的病变。准确诊断需要了解PRA处ECM的发生情况并识别其特征性细胞形态。本文展示了我们病例的TI细胞学特征,并回顾了既往报道的ECM细胞学及诊断陷阱。《诊断细胞病理学》2016年;44:618 - 622。© 2016威利期刊公司

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