Canacci Anastasia M, Nunez Carlos, Getty Patrick, Abdul-Karim Fadi
Department of Pathology, University Hospitals Case Medical Center Cleveland, Ohio 44106, USA.
Acta Cytol. 2010 Mar-Apr;54(2):190-2. doi: 10.1159/000325007.
Malignant granular cell tumor (GCT) is a rare sarcoma that is often difficult to differentiate histologically from its benign counterpart.
A 69-year-old Caucasian man with a long history of multiple GCTs presented with new-onset left shoulder pain and limitation of movement. Radiographic studies revealed a lytic lesion within the left humeral metaphysis and a pathologic fracture. Computed tomography-guided fine needle aspiration and needle core biopsies were performed. The patient subse quently underwent curettage of the tumor with prophylactic fixation of the left proximal humerus. He received postsurgical radiation and physical therapy.
The diagnosis of metastatic malignant GCT was rendered in this case. The fne needle aspiration ofmetastatic GCT may lack cytologic features of malignancy. The diagnosis necessitates clinical correlation and an understanding of the spectrum of histopathologic changes in GCT and malignant
恶性颗粒细胞瘤(GCT)是一种罕见的肉瘤,在组织学上常常难以与其良性对应物相鉴别。
一名69岁的白人男性,有多个GCT的长期病史,出现新发的左肩疼痛和活动受限。影像学检查显示左肱骨干骺端有一个溶骨性病变和一处病理性骨折。进行了计算机断层扫描引导下的细针穿刺抽吸和针芯活检。患者随后接受了肿瘤刮除术并对左肱骨近端进行了预防性固定。他接受了术后放疗和物理治疗。
本例诊断为转移性恶性GCT。转移性GCT的细针穿刺抽吸可能缺乏恶性的细胞学特征。诊断需要临床关联以及对GCT和恶性肿瘤组织病理学变化范围的了解。