一名有睾丸精瘤生殖细胞肿瘤史的患者。病例报告和文献综述

IF 0.1 Q4 ONCOLOGY
Mayra Cristina Galeana-Hernández , Jorge Martínez-Cedillo , Leopoldo Abraham Lugo-Alférez
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引用次数: 0

摘要

睾丸生殖细胞瘤是最可治愈的实体瘤,10年后的相对总生存率超过95%。大多数患者的治愈率和长期存活率引起了对与治疗相关的副作用的兴趣。第二,恶性肿瘤是影响幸存者预后的最严重的副作用之一。本研究的目的是描述一名半瘤型睾丸癌患者的病例,他在20年后出现了第二次原发性肿瘤。文献综述也提出。该病例涉及一名68岁的患者,有吸烟史,烟草指数为45,双侧隐睾和39岁的兰花切除术。诊断为右侧睾丸癌,腹膜后有一个8 × 8厘米的肿瘤。1993年,进行了根治性睾丸切除术,随后进行了化疗,治疗效果良好。二十年后,患者出现口腔耐受不良,胃脘痛,内窥镜显示为Bormann III型胃癌。组织病理学报告描述了一种低分化腺癌,弥漫着印戒细胞。计算机断层显示腹膜癌的证据。通过化疗和/或放疗治愈的生殖细胞癌存活患者面临治疗的长期影响,包括化疗相关毒性和第二原发肿瘤的出现,包括原发肿瘤诊断后长达30年的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Segundo primario en un paciente con antecedente de tumor germinal seminomatoso de testículo. Reporte del caso y revisión de la literatura

The testicular germ cell tumour is the most curable solid tumour, with a relative overall survival rate of more than the 95% after 10 years. The cure rate and long term survival of the majority of the patients has led to an interest in the side effects related to the treatment. Second malignant tumours are one of the most serious side effects that compromise the prognosis of the survivors. The aim of the present study is describe the case of one patient with seminomatous type testicular cancer, who presented with a second primary after 20 years. A literature review is also presented.

The case concerns a 68 year-old patient, with a smoking history with a tobacco index of 45, bilateral cryptorchidism, and an orchidopexy at 39 years old. Cancer was diagnosed in the right testicle with an 8 × 8 cm retroperitoneal tumour. In 1993, a radical orchiectomy was performed, followed by chemotherapy, with full response to the treatment. Twenty years later, he had oral intolerance, epigastralgia, with endoscopic evidence of a Bormann III gastric tumour. The histopathological report described a poorly differentiated adenocarcinoma, diffuse with signet ring cells. The computed tomography showed evidence of peritoneal carcinomatosis.

Surviving patients of germ cell cancer, cured with chemotherapy and/or radiotherapy, face the long-term effects of the treatment, including chemotherapy related toxicity and the appearance of a second primary, including a risk up to 30 years after diagnosis of primary tumour.

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