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一名接受骨髓移植患者的巨细胞成纤维细胞瘤。

Giant-cell fibroblastoma in a patient with a bone-marrow transplant.

作者信息

Carroll D, Ramani P, Lander A D

机构信息

Department of Paediatric Surgery, Bristol Royal Hospital for Sick Children, St. Michael's Hill, Bristol, BS8 2BJ, UK.

出版信息

Pediatr Surg Int. 2003 Aug;19(6):495-6. doi: 10.1007/s00383-002-0827-y. Epub 2003 Jun 13.

DOI:10.1007/s00383-002-0827-y
PMID:12820000
Abstract

A case of an epigastric giant-cell fibroblastoma is reported in a 6-year-old girl who had undergone a bone-marrow transplant for severe combined immunodeficiency secondary to adenosine deaminase deficiency. A small subcutaneous nodule had been excised from the epigastrium at age 12 months.

摘要

报道了一例6岁女孩的上腹部巨细胞成纤维细胞瘤病例,该女孩因腺苷脱氨酶缺乏继发严重联合免疫缺陷而接受了骨髓移植。患儿12个月大时,上腹部一个小的皮下结节已被切除。

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1
Giant-cell fibroblastoma in a patient with a bone-marrow transplant.一名接受骨髓移植患者的巨细胞成纤维细胞瘤。
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Composite tumor consisting of dermatofibrosarcoma protuberans and giant cell fibroblastoma associated with intratumoral endometriosis. Report of a case.由隆突性皮肤纤维肉瘤和巨细胞成纤维细胞瘤组成并伴有瘤内子宫内膜异位症的复合性肿瘤。病例报告。
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引用本文的文献

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Long-Term Outcome of Adenosine Deaminase-Deficient Patients-a Single-Center Experience.腺苷脱氨酶缺乏症患者的长期预后:单中心经验。
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Multicentric dermatofibrosarcoma protuberans in patients with adenosine deaminase-deficient severe combined immune deficiency.多发性局灶性纤维组织细胞瘤在腺苷脱氨酶缺陷严重联合免疫缺陷症患者中。
J Allergy Clin Immunol. 2012 Mar;129(3):762-769.e1. doi: 10.1016/j.jaci.2011.10.028. Epub 2011 Dec 6.

本文引用的文献

1
Immunological surveillance in neoplasia.肿瘤中的免疫监视
Transplant Rev. 1971;7:3-25. doi: 10.1111/j.1600-065x.1971.tb00461.x.
2
Giant cell fibroblastoma. A distinctive, recurrent tumor of childhood.巨细胞成纤维细胞瘤。一种独特的儿童复发性肿瘤。
Am J Surg Pathol. 1987 Apr;11(4):263-71.
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Giant cell fibroblastoma of soft tissue: a clinicopathological and immunohistochemical study.
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Giant cell fibroblastoma: a report of three cases.
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Giant cell fibroblastoma. A juvenile form of dermatofibrosarcoma protuberans.
Cancer. 1989 Nov 15;64(10):2154-61. doi: 10.1002/1097-0142(19891115)64:10<2154::aid-cncr2820641030>3.0.co;2-n.