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颌骨混合性中央巨细胞肉芽肿和中央性牙源性纤维瘤样病变

Hybrid central giant cell granuloma and central odontogenic fibroma-like lesions of the jaws.

作者信息

Odell E W, Lombardi T, Barrett A W, Morgan P R, Speight P M

机构信息

Department of Oral Medicine and Pathology, UMDS Guy's Hospital, London, UK.

出版信息

Histopathology. 1997 Feb;30(2):165-71. doi: 10.1046/j.1365-2559.1997.d01-585.x.

Abstract

Ten lesions from eight cases are presented of a rare intra-osseous jaw lesion with the combined histological features of giant cell granuloma and central odontogenic fibroma. Lesions arose over a wide age range and presented as monolocular or multilocular radiolucencies with cortical expansion and, in one case, perforation. Two lesions recurred after curettage, one being eradicated by a second curettage and one by conservative excision. Histologically, zones of typical giant cell granuloma lay in a fibrous stroma containing islands, strands and clusters of epithelial cells. Islands often contained duct-like spaces or hyaline basement membrane globules. Trabeculae of osteoid were present in five lesions. Recurrent lesions showed features identical to the initial lesion, including recurrence of the prominent epithelial component. These features cannot be conclusively ascribed to a variant of either giant cell granuloma, central odontogenic fibroma or aneurysmal bone cyst, but the clinical features are slightly more suggestive of giant cell granuloma. Attention is drawn to the characteristic and potentially confusing histological appearances. The presence of giant cell granuloma-like areas in central odontogenic fibroma-like lesions is associated with an increased risk of recurrence following curettage.

摘要

本文呈现了8例患者的10处病损,这些病损是一种罕见的颌骨骨内病变,具有巨细胞肉芽肿和中央性牙源性纤维瘤的联合组织学特征。病损发生于较广的年龄范围,表现为单房或多房的透射影,伴有皮质膨胀,其中1例出现穿孔。2处病损刮除术后复发,1例经再次刮除治愈,1例经保守切除治愈。组织学上,典型的巨细胞肉芽肿区域位于含有上皮细胞岛、条索和团块的纤维性基质中。上皮岛常含有导管样间隙或透明基底膜小球。5处病损中有类骨质小梁。复发病损表现出与初始病损相同的特征,包括显著上皮成分的复发。这些特征不能明确归为巨细胞肉芽肿、中央性牙源性纤维瘤或动脉瘤样骨囊肿的变异型,但临床特征稍更提示巨细胞肉芽肿。文中提请注意其特征性且可能混淆的组织学表现。中央性牙源性纤维瘤样病变中存在巨细胞肉芽肿样区域与刮除术后复发风险增加相关。

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