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异基因骨髓移植治疗急性淋巴细胞白血病 11 年后发生食管鳞状细胞癌。

Esophageal squamous cell carcinoma developed 11 years after allogeneic bone marrow transplantation for acute lymphatic leukemia.

机构信息

Department of Esophago-Gastric Surgery, Tokyo Medical and Dental University, 1-5-45 Yushima, Bunkyo-ku, Tokyo 113-8519, Japan.

出版信息

Jpn J Clin Oncol. 2013 Jan;43(1):69-73. doi: 10.1093/jjco/hys184. Epub 2012 Dec 4.

Abstract

Younger patients (aged <30 years) presenting with esophageal cancer are rare. Bone marrow transplantation offers a curative therapy in patients with malignant and nonmalignant lymphohematopoietic diseases and other disorders. However, one important late complication in transplantation survivors is the development of secondary malignancies including solid tumors. Although some solid cancers have been demonstrated to occur after bone marrow transplantation, only a few cases of esophageal squamous cell carcinoma have thus far been reported. We herein describe the case of a 27-year-old male with esophageal squamous cell carcinoma, who was diagnosed with T-cell-type acute lymphatic leukemia at the age of 12 and relapsed 5 years later. He achieved a second complete remission and underwent bone marrow transplantation at the age of 17. A genetic analysis revealed germ-line lineage-derived chimeric cellular populations of the donor and patient on both the esophageal squamous cell carcinoma and non tumorous portions of the patient's esophageal mucosa with a preponderance of the patient's germ-line lineage-derived cells, suggesting that repopulated donor-derived hemopoietic stem cells in the esophageal epithelia only partially contributed to the carcinogenesis of esophageal squamous cell carcinoma several years after bone marrow transplantation. Multiple events occurring during the course of treatment for primary hematological disorder may play an important role in the development of esophageal squamous cell carcinoma.

摘要

年轻患者(<30 岁)患食管癌较为罕见。骨髓移植为恶性和非恶性淋巴血液疾病和其他疾病患者提供了一种治愈疗法。然而,移植幸存者的一个重要晚期并发症是发展为继发性恶性肿瘤,包括实体瘤。虽然已经证实某些实体瘤发生在骨髓移植后,但迄今为止仅报告了少数几例食管鳞状细胞癌病例。我们在此描述了一例 27 岁男性,患有食管鳞状细胞癌,他在 12 岁时被诊断为 T 细胞型急性淋巴细胞白血病,5 年后复发。他实现了第二次完全缓解,并在 17 岁时进行了骨髓移植。遗传分析显示,供体和患者的源自种系的嵌合细胞群体存在于患者食管黏膜的食管鳞状细胞癌和非肿瘤部分,患者的源自种系的细胞占优势,表明在骨髓移植后数年,重新填充的供体衍生造血干细胞仅部分促成了食管鳞状细胞癌的发生。在原发性血液系统疾病治疗过程中发生的多种事件可能在食管鳞状细胞癌的发展中起重要作用。

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