Department of Pathology.
Departments of Pathology, Neurology and Neurosurgery, University of Colorado, Aurora, Colorado.
J Neuropathol Exp Neurol. 2019 Dec 1;78(12):1171-1173. doi: 10.1093/jnen/nlz100.
Giant cell tumor (GCT) of bone is a locally aggressive tumor with low metastatic potential, usually originating in long bones. Numerous spinal examples have been reported and thus GCTs can be encountered by neuropathologists. We describe a 69-year-old man with more than a 10-year history of GCT primary to the femur that had recently metastasized to the occipital skull bone. The patient had been receiving denosumab, an adjuvant therapy for GCT, prior to the metastasis. Review of the histological features of the original primary tumor in the femur showed archetypal features of GCT, but the posttreatment occipital skull metastasis showed a predominantly low-to-medium cell density spindle cell tumor with complete depletion of osteoclastic giant cells. Although this effect of the drug is increasingly being recognized by soft tissue pathologists, the current case illustrates the potentially confusing histology of postdenosumab-treated GCT for neuropathologists. The absence of giant cells leads the posttherapy primary or metastatic lesion to show histologic similarity to a multitude of benign and malignant fibro-osseous lesions or spindle cell sarcoma and highlights the importance of eliciting appropriate clinical history.
骨巨细胞瘤(GCT)是一种局部侵袭性肿瘤,转移潜能低,通常起源于长骨。已有大量脊柱病例报道,因此神经病理学家也可能会遇到 GCT。我们描述了一名 69 岁男性,其股骨原发 GCT 病史超过 10 年,最近已转移至枕骨颅骨。该患者在转移前曾接受地舒单抗(一种 GCT 的辅助治疗药物)治疗。对股骨原发肿瘤的组织学特征进行回顾,显示出典型的 GCT 特征,但治疗后枕骨颅骨转移表现为以中低细胞密度为主的梭形细胞肿瘤,破骨细胞性巨细胞完全耗竭。虽然软组织病理学家越来越多地认识到这种药物的作用,但目前的病例说明了神经病理学家在处理地舒单抗治疗后的 GCT 时可能会出现混淆的组织学表现。巨细胞的缺失导致治疗后原发或转移病变的组织学表现与多种良性和恶性纤维骨病变或梭形细胞肉瘤相似,突出了获取适当临床病史的重要性。