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传统型骨巨细胞瘤的自发恶性转化

Spontaneous malignant transformation of conventional giant cell tumor.

作者信息

Grote H J, Braun M, Kalinski T, Pomjanski N, Back W, Bleyl U, Böcking A, Roessner A

机构信息

Institute of Cytopathology, Heinrich Heine University, Moorenstrasse 5, D-40225 Düsseldorf, Germany.

出版信息

Skeletal Radiol. 2004 Mar;33(3):169-75. doi: 10.1007/s00256-003-0682-5. Epub 2004 Jan 29.

Abstract

Spontaneous malignant transformation of conventional giant cell tumor (GCT) of bone is exceedingly rare. We report on a case of GCT of the iliac crest in a 35-year-old woman with malignant change into a high-grade osteosarcoma 10 years after the first appearance of GCT on a radiograph. Since the patient refused therapy for personal reasons the tumor remained untreated until sarcomatous transformation occurred. Image cytometry showed DNA aneuploidy and a suspiciously high 2c deviation index (2cDI) in the primary bone lesion. A thorough review of the world literature revealed only seven fully documented cases of secondary malignant GCT which matched the definition of a "sarcomatous growth that occurs at the site of a previously documented benign giant cell tumor" and not treated by radiotherapy. These cases as well as the current one suggest that a spontaneous secondary malignant GCT presents as a frankly sarcomatous tumor in the form of an osteosarcoma or malignant fibrous histiocytoma. It usually appears at sites of typical GCTs-often without any recurrent intermediate state-and is diagnosed 3 or more years after the primary bone lesion. The prognosis is poor.

摘要

骨传统型巨细胞瘤(GCT)的自发恶性转变极为罕见。我们报告一例35岁女性的髂嵴GCT病例,该病例在X线片首次出现GCT 10年后恶变为高级别骨肉瘤。由于患者出于个人原因拒绝治疗,肿瘤一直未得到治疗,直至发生肉瘤样转变。图像细胞术显示原发性骨病变中存在DNA非整倍体以及可疑的高2c偏差指数(2cDI)。对世界文献的全面回顾仅发现7例有充分记录的继发性恶性GCT病例,这些病例符合“在先前记录的良性巨细胞瘤部位发生的肉瘤样生长”的定义且未接受放疗。这些病例以及当前这例表明,自发继发性恶性GCT表现为骨肉瘤或恶性纤维组织细胞瘤形式的明显肉瘤样肿瘤。它通常出现在典型GCT的部位,常常没有任何复发的中间状态,且在原发性骨病变后3年或更长时间被诊断出来。预后很差。

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