Oda Yoshinao, Takahira Tomonari, Yokoyama Ryohei, Tsuneyoshi Masazumi
Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Higashi-ku, Fukuoka, Japan. surgpath.med.kyushi-u.ac.jp
Pathol Int. 2007 Sep;57(9):627-31. doi: 10.1111/j.1440-1827.2007.02150.x.
Diffuse-type giant cell tumor (GCT)/pigmented villonodular synovitis (PVNS) in the axial skeleton or spine is rare. Herein is reported a case of diffuse-type GCT/PVNS involving the sacrum and the fifth lumbar vertebra, in which the patient developed regional lymph node swelling after recurrence. The recurrent tumor was found to have atypical histological features such as spindle cell morphology, cytological atypia and high mitotic rate, which are compatible with the diagnostic criteria of secondary malignant diffuse-type GCT/PVNS. Although the nodal lesions were not sampled histologically, the clinical and histological features indicate that the current case is an example of malignant diffuse-type GCT/PVNS. This case is considered to be the first case of malignant diffuse-type GCT/PVNS in the spine, because no such lesions have been previously reported in the axial skeleton or spine. Careful surveillance should be required for diffuse-type GCT/PVNS arising at unusual site.
弥漫型巨细胞瘤(GCT)/色素沉着绒毛结节性滑膜炎(PVNS)累及中轴骨骼或脊柱较为罕见。本文报告1例累及骶骨和第5腰椎的弥漫型GCT/PVNS,该患者复发后出现区域淋巴结肿大。复发肿瘤具有非典型组织学特征,如梭形细胞形态、细胞异型性和高有丝分裂率,符合继发性恶性弥漫型GCT/PVNS的诊断标准。尽管未对淋巴结病变进行组织学取样,但临床和组织学特征表明本例为恶性弥漫型GCT/PVNS。该病例被认为是脊柱恶性弥漫型GCT/PVNS的首例,因为此前在中轴骨骼或脊柱中未报告过此类病变。对于发生在不寻常部位的弥漫型GCT/PVNS,应进行仔细监测。