Gleason Briana C, Kleinman Paul K, Debelenko Larisa V, Rahbar Reza, Gebhardt Mark C, Perez-Atayde Antonio R
Department of Pathology, Children's Hospital, Boston, MA 02115, USA.
Am J Surg Pathol. 2007 Jun;31(6):926-32. doi: 10.1097/PAS.0b013e31802fb498.
Giant cell-rich lesions of bone, including giant cell tumor of bone, giant cell reparative granuloma (GCRG), and aneurysmal bone cyst (ABC), may have overlapping clinical, radiologic, and histopathologic features. In fact, GCRG and solid ABC are currently differentiated solely based on skeletal location. Prior cytogenetic studies have reported that telomeric associations are present in the majority of giant cell tumors of bone, whereas translocations involving 16q22 and/or 17p13 are characteristic of ABCs. There is only one previously published karyotype of a GCRG, which revealed a reciprocal translocation, t(X;4)(q22;q31.3). We report 3 cases of giant cell-rich bone lesions with novel karyotypes: one lesion located in the first metacarpal, a typical location for GCRG, was histologically consistent with a giant cell tumor and showed the following karyotype [46,XX,inv(2)(p13q21),t(inv2;11)(q21;q13)]; the second lesion, also a giant cell tumor of bone, in the sacrum showed the following karyotype [46,XX,r(9)(p24q34)[cp7]/46,idem,?r(16)(p13.3q24)[cp10]/46,XX]. The third lesion, a hard palate mass, had the histopathologic features of a GCRG and a karyotype showing a reciprocal translocation, 46,XY,t(2;10)(q23;q24). These findings suggest that at least a subset of GCRGs may be neoplastic and that these lesions differ cytogenetically from classic giant cell tumors of bone or solid ABC, although the latter entity is otherwise indistinguishable from reparative granuloma. Further cytogenetic characterization of giant cell-rich bone lesions may improve the utility of karyotyping as a tool in their differential diagnosis and may shed light on the pathogenetic relationship between these lesions.
富含巨细胞的骨病变,包括骨巨细胞瘤、巨细胞修复性肉芽肿(GCRG)和骨动脉瘤样囊肿(ABC),可能具有重叠的临床、放射学和组织病理学特征。事实上,目前GCRG和实性ABC仅根据骨骼位置进行区分。先前的细胞遗传学研究报告称,大多数骨巨细胞瘤存在端粒关联,而涉及16q22和/或17p13的易位是ABC的特征。之前仅发表过一份GCRG的核型,显示为相互易位,t(X;4)(q22;q31.3)。我们报告3例具有新核型的富含巨细胞的骨病变:1例位于第一掌骨,这是GCRG的典型部位,组织学上与骨巨细胞瘤一致,核型为[46,XX,inv(2)(p13q21),t(inv2;11)(q21;q13)];第2例也是骨巨细胞瘤,位于骶骨,核型为[46,XX,r(9)(p24q34)[cp7]/46,idem,?r(16)(p13.3q24)[cp10]/46,XX]。第3例病变为硬腭肿物,具有GCRG的组织病理学特征,核型显示为相互易位,46,XY,t(2;10)(q23;q24)。这些发现表明,至少一部分GCRG可能是肿瘤性的,并且这些病变在细胞遗传学上与经典的骨巨细胞瘤或实性ABC不同,尽管后者在其他方面与修复性肉芽肿难以区分。对富含巨细胞的骨病变进行进一步的细胞遗传学特征分析,可能会提高核型分析作为鉴别诊断工具的实用性,并可能揭示这些病变之间的发病机制关系。