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成釉细胞瘤。一例经穿刺细胞学检查、鉴别诊断及免疫组化分析的病例报告。

Adamantinoma. A case report with aspiration cytology and differential diagnostic and immunohistochemical considerations.

作者信息

Laucirica R, Mody D, MacLeay L, Kearns R J, Ramzy I

机构信息

Department of Pathology, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Acta Cytol. 1992 Nov-Dec;36(6):951-6.

PMID:1449035
Abstract

Fine needle aspiration biopsy of bone lesions is routinely used in the metastatic workup of patients with radiographically suspicious areas. However, caution must be used when interpreting smears from aspirates performed on primary bone neoplasms. These tumors are often heterogeneous, and problems with sampling may be encountered. We report a case of a 25-year-old male who presented with a 3-cm lytic lesion in the tibia. A diagnosis of benign fibroosseous lesion was based on the clinical presentation, radiographic appearance and presence of numerous sheets and single cytologically bland spindle cells. Subsequent curettage of the specimen revealed an adamantinoma with a prominent fibrous component. Most of these rare, locally aggressive neoplasms are located in the tibia. They are characterized histologically as having a fibrous background with islands of basaloid, spindle or squamoid cells. Furthermore, a differentiated, regressing variant with an osteofibrous dysplasia-like appearance also exists. Smears consisting primarily of spindle cells or fibrous tissue may lead to an erroneous diagnosis of a fibrohistiocytic neoplasm, fibrous dysplasia, fibrous cortical defect or ossifying fibroma. Pertinent cytomorphologic features should aid in establishing the correct diagnosis of adamantinoma.

摘要

骨病变的细针穿刺活检常用于对影像学检查有可疑区域的患者进行转移灶检查。然而,在解读原发性骨肿瘤穿刺涂片时必须谨慎。这些肿瘤通常具有异质性,可能会遇到取材问题。我们报告一例25岁男性患者,其胫骨出现一个3厘米的溶骨性病变。根据临床表现、影像学表现以及存在大量成片和单个细胞形态温和的梭形细胞,诊断为良性纤维骨性病变。随后对标本进行刮除术,结果显示为具有显著纤维成分的造釉细胞瘤。这些罕见的、局部侵袭性肿瘤大多位于胫骨。它们在组织学上的特征是具有纤维背景,伴有基底样、梭形或鳞状细胞岛。此外,还存在一种具有骨纤维发育异常样外观的分化、消退型。主要由梭形细胞或纤维组织组成的涂片可能会导致错误诊断为纤维组织细胞瘤、纤维发育异常、纤维皮质缺损或骨化性纤维瘤。相关的细胞形态学特征应有助于确立造釉细胞瘤的正确诊断。

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