Metastatic Testicular Cancer Complicated by Myelodysplastic Syndrome

IF 0.5 Q4 Medicine
Nobuhiko Shimizu, Tomoki Okada, Ryuga Kato, Sosuke Niwa, Takahiro Yanase, Rei Unno, Shoichiro Iwatsuki, Toshiki Etani, Atsushi Okada, Takahiro Yasui
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引用次数: 0

Abstract

Introduction

The coexistence of testicular cancer and hematopoietic disorders is rare, and reports on optimal treatment strategies are limited. Here, we present a case of metastatic testicular cancer associated with myelodysplastic syndrome.

Case Presentation

A 24-year-old man with pancytopenia underwent right orchiectomy for a right scrotal mass. Histopathological examination revealed embryonal carcinoma. Subsequent imaging demonstrated para-aortic lymph node metastasis. Pancytopenia was diagnosed as myelodysplastic syndrome. The patient received chemotherapy with dose modifications and a prolonged treatment course, followed by retroperitoneal lymph node dissection; viable tumor cells were identified in the resected specimens. After adjuvant chemotherapy, allogenic hematopoietic stem cell transplantation was performed for myelodysplastic syndrome. The patient remained free of testicular cancer recurrence for 2 years post-surgery.

Conclusion

This case suggests that durable disease control may be achievable in metastatic testicular cancer associated with myelodysplastic syndrome through carefully managed chemotherapy and surgery.

转移性睾丸癌合并骨髓增生异常综合征
摘要睾丸癌与造血系统疾病共存的情况很少见,关于最佳治疗策略的报道也很有限。在此,我们报告一例转移性睾丸癌合并骨髓增生异常综合征。一例24岁男性全血细胞减少症患者因右侧阴囊肿块行右侧睾丸切除术。组织病理学检查显示胚胎癌。随后影像学显示主动脉旁淋巴结转移。全血细胞减少症诊断为骨髓增生异常综合征。患者接受剂量调整和延长疗程的化疗,随后进行腹膜后淋巴结清扫;在切除的标本中发现了活的肿瘤细胞。辅助化疗后,行异基因造血干细胞移植治疗骨髓增生异常综合征。患者术后2年无睾丸癌复发。结论本病例提示,通过精心管理的化疗和手术,转移性睾丸癌伴骨髓增生异常综合征的患者可以获得持久的疾病控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IJU Case Reports
IJU Case Reports Medicine-Urology
CiteScore
0.60
自引率
0.00%
发文量
147
审稿时长
15 weeks
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