Shahrokh Soroush, Tran Daniel, Lines Barbara, Bhuriwala Murtaza N
Graduate Medical Education, HCA Houston Healthcare Kingwood Medical Center/University of Houston College of Medicine, Kingwood, USA.
Internal Medicine Residency Program/Internal Medicine, HCA Houston Healthcare Kingwood Medical Center/University of Houston College of Medicine, Kingwood, USA.
Cureus. 2022 Mar 6;14(3):e22885. doi: 10.7759/cureus.22885. eCollection 2022 Mar.
A 25-year-old male presented to our hospital with two months of progressively worsening left arm swelling, intermittent left-sided chest pressure, and a painless right testicular mass. CT of the chest, abdomen, and pelvis revealed a large mediastinal mass, multiple lung nodules, and several large right testicular nodules. The patient underwent a CT-guided biopsy of his right lung nodule, followed by a radical right inguinal orchiectomy. The testicular biopsy revealed a mixed germ cell tumor (GCT) consisting of 97% seminoma and 3% teratoma, while the lung biopsy revealed metastatic choriocarcinoma. The patient was treated with four cycles of bleomycin, etoposide, and platinum (BEP) and showed a great clinical response, with only residual disease in his retroperitoneal lymph nodes. He was referred for retroperitoneal lymph node dissection (RPLND); however, there was a delay of several months, which led to the recurrence of his disease. He received four cycles of paclitaxel, ifosfamide, and cisplatin and showed a moderate response. He later received salvage chemotherapy with high-dose carboplatin and etoposide and underwent bone-marrow transplant, leading to complete clinical response and eradication of his disease. There are different subtypes of testicular GCTs, each with distinct pathogenesis, treatment modality, and prognosis. In this report, we discuss the case of a patient who presented with a mixed GCT consisting of seminoma and teratoma in his testicle, which had metastasized as choriocarcinoma to his lung and mediastinum. This report elucidates the potential for testicular GCTs to metastasize as a pathologically different cancer compared to the primary tumor. This phenomenon has significant clinical ramifications, as it can considerably alter a patient's treatment and prognostic outcomes.
一名25岁男性因左臂肿胀进行性加重两个月、左侧胸部间歇性压迫感以及右侧睾丸无痛性肿块前来我院就诊。胸部、腹部和骨盆CT显示纵隔有一个大肿块、多个肺结节以及几个右侧睾丸大结节。患者接受了右肺结节的CT引导下活检,随后进行了根治性右腹股沟睾丸切除术。睾丸活检显示为混合性生殖细胞肿瘤(GCT),由97%的精原细胞瘤和3%的畸胎瘤组成,而肺活检显示为转移性绒毛膜癌。患者接受了四个周期的博来霉素、依托泊苷和顺铂(BEP)治疗,临床反应良好,仅腹膜后淋巴结有残留病灶。他被转诊进行腹膜后淋巴结清扫术(RPLND);然而,出现了数月的延迟,导致疾病复发。他接受了四个周期的紫杉醇、异环磷酰胺和顺铂治疗,反应中等。他后来接受了大剂量卡铂和依托泊苷的挽救化疗并进行了骨髓移植,实现了完全临床缓解并根除了疾病。睾丸GCT有不同的亚型,每种亚型都有独特的发病机制、治疗方式和预后。在本报告中,我们讨论了一名患者的病例,该患者睾丸出现由精原细胞瘤和畸胎瘤组成的混合性GCT,并已转移为绒毛膜癌至肺部和纵隔。本报告阐明了睾丸GCT与原发性肿瘤相比,有可能转移为病理类型不同的癌症。这种现象具有重要的临床意义,因为它会显著改变患者的治疗和预后结果。