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骨外黏液样软骨肉瘤的骨骼复发和转移

Skeletal recurrences and metastases of extraskeletal myxoid chondrosarcoma.

作者信息

Ehara Shigeru, Nishida Jun, Shiraishi Hideo, Yoshioka Hiroshi, Okada Kyoji, Sumiya Hisashi, Takano Hideyuki

机构信息

Department of Radiology, Iwate Medical University School of Medicine, 19-1 Uchimaru, Morioka 020-8505, Japan.

出版信息

Skeletal Radiol. 2007 Sep;36(9):823-7. doi: 10.1007/s00256-007-0303-9. Epub 2007 Apr 17.

DOI:10.1007/s00256-007-0303-9
PMID:17437101
Abstract

OBJECTIVE

The objective was to elucidate clinical and imaging features of skeletal involvement, recurrences, and metastases of extraskeletal myxoid chondrosarcoma.

MATERIALS AND METHODS

Included in this series are 4 patients, aged 44 to 65 years, 3 of whom were men and 1 a woman.

RESULTS

The primary lesions were in the thigh (n = 3) and the upper arm (n = 1). Three patients with multiple metastases died of the disease, 2 were considered to have local recurrence in the adjacent bone. Skeletal metastases occurred after lung metastases in 2 cases, and before lung metastases in 1 case. Typical imaging findings are well-defined lesions with no sclerotic margin or matrix mineralization. A slow, but persistent growth is noted on the imaging features.

CONCLUSION

Although skeletal metastases of chondrosarcoma of bone and soft tissue are rare, myxoid chondrosarcomas, currently classified tumors of uncertain differentiation, rarely metastasize and/or recur in the bones. The imaging features are typically of a localized lesion with cortical disruption or expansion.

摘要

目的

旨在阐明骨外黏液样软骨肉瘤骨骼受累、复发及转移的临床和影像学特征。

材料与方法

本系列纳入4例患者,年龄44至65岁,其中3例为男性,1例为女性。

结果

原发灶位于大腿(n = 3)和上臂(n = 1)。3例发生多处转移的患者死于该疾病,2例被认为在相邻骨出现局部复发。2例骨骼转移发生在肺转移之后,1例发生在肺转移之前。典型的影像学表现为边界清晰的病变,无硬化边缘或基质矿化。影像学特征显示生长缓慢但持续。

结论

尽管骨和软组织软骨肉瘤的骨骼转移罕见,但黏液样软骨肉瘤(目前分类为分化不确定的肿瘤)很少在骨骼中发生转移和/或复发。影像学特征通常为伴有皮质破坏或膨胀的局限性病变。

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本文引用的文献

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Extraskeletal myxoid chondrosarcoma: updated clinicopathological and molecular genetic characteristics.骨外黏液样软骨肉瘤:更新的临床病理及分子遗传学特征
Pathol Int. 2005 Aug;55(8):453-63. doi: 10.1111/j.1440-1827.2005.01853.x.
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Extraskeletal myxoid chondrosarcoma: a Multi-Institutional Study of 42 Cases in Japan.骨外黏液样软骨肉瘤:日本42例多机构研究。
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Extraskeletal myxoid chondrosarcoma with multiple skeletal metastases.伴有多发骨转移的骨外黏液样软骨肉瘤
J Orthop Sci. 2000;5(2):171-4. doi: 10.1007/s007760050145.
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Extraskeletal myxoid chondrosarcoma: a clinicopathologic, immunohistochemical, and ploidy analysis of 23 cases.骨外黏液样软骨肉瘤:23例临床病理、免疫组化及倍体分析
Mod Pathol. 2000 Aug;13(8):900-8. doi: 10.1038/modpathol.3880161.
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Extraskeletal myxoid chondrosarcoma: multimodal diagnosis and identification of a new cytogenetic subgroup characterized by t(9;17)(q22;q11).骨外黏液样软骨肉瘤:多模态诊断及一个以t(9;17)(q22;q11)为特征的新细胞遗传学亚组的鉴定
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Skeletal Radiol. 1993 Nov;22(8):595-9. doi: 10.1007/BF00197142.
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Hum Pathol. 1972 Sep;3(3):421-35. doi: 10.1016/s0046-8177(72)80042-x.
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Myxoid chondrosarcoma with a translocation involving chromosomes 9 and 22.伴有9号和22号染色体易位的黏液样软骨肉瘤。
Cancer Genet Cytogenet. 1985 Jan 15;14(3-4):219-26. doi: 10.1016/0165-4608(85)90187-6.
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Recurrent breakpoints at 9q31 and 22q12.2 in extraskeletal myxoid chondrosarcoma.骨外黏液样软骨肉瘤中9q31和22q12.2处的复发性断点。
Cancer Genet Cytogenet. 1988 Jan;30(1):145-50. doi: 10.1016/0165-4608(88)90103-3.