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一例表现为皮肤亲表皮性肿瘤且潜伏期短的放射性诱发颅骨骨肉瘤病例。

A case of radiation-induced osteosarcoma of the skull presenting as a cutaneous epidermotropic tumor with a short latent period.

作者信息

Rashidghamat Elham, Calonje Jaime Eduardo

机构信息

St. John's Institute of Dermatology, Guy's and St Thomas' NHS Trust, London, UK.

出版信息

J Cutan Pathol. 2018 May;45(5):352-354. doi: 10.1111/cup.13103. Epub 2018 Mar 12.

DOI:10.1111/cup.13103
PMID:29330865
Abstract

Radiation-induced sarcoma (RIS) is an unusual but well documented tumor. The frequency of RIS of the head and neck region has been reported as 0.143%. In the literature the median interval between irradiation and development of sarcoma is 11 years. Cases of RIS with a short latent period, that is, less than 4 years are rare. We report a case of a 34-year-old female who developed an osteosarcoma of the scalp, over a previous craniotomy scar, 3 years after excision of a frontal anaplastic oligodendroglioma which had been followed by a course of 6 weeks radiotherapy (58 Gy) and 6 cycles of temozolomide. The histological features were those of a high-grade osteosarcoma with epidermotropism of tumor cells. Lymph nodes were partially replaced by high-grade metastatic osteosarcoma, with extra-nodal lymphatic tumor thrombi. To our knowledge the only other case report of post-radiation osteosarcoma with a short latency period was a case of osteosarcoma in the craniofacial bone 3 years after radiotherapy for maxillary squamous cell carcinoma. The histological finding of prominent replacement of the epidermis by osteosarcoma has not been reported before.

摘要

放射性肉瘤(RIS)是一种罕见但有充分文献记载的肿瘤。头颈部RIS的发生率据报道为0.143%。文献中肉瘤发生与放疗之间的中位间隔时间为11年。潜伏期短(即少于4年)的RIS病例罕见。我们报告一例34岁女性,在切除额叶间变性少突胶质细胞瘤并接受6周放疗(58 Gy)及6个周期替莫唑胺治疗3年后,在既往开颅手术瘢痕处发生头皮骨肉瘤。组织学特征为高级别骨肉瘤伴肿瘤细胞亲表皮性。淋巴结部分被高级别转移性骨肉瘤取代,伴有结外淋巴管肿瘤血栓形成。据我们所知,另一例放疗后潜伏期短的骨肉瘤病例报告是上颌鳞状细胞癌放疗3年后发生在颅面骨的骨肉瘤。骨肉瘤显著取代表皮的组织学表现此前未见报道。

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