Sakamaki Yasushi, Kogita Yuya, Minami Seigo, Azuma Kouji, Kou Yuuki, Matsuda Ryosuke, Goto Takayoshi
Department of Thoracic Surgery, Osaka Keisatsu Hospital, Osaka, JPN.
Department of Respiratory Medicine, National Hospital Organization Osaka Medical Center, Osaka, JPN.
Cureus. 2025 Jun 22;17(6):e86526. doi: 10.7759/cureus.86526. eCollection 2025 Jun.
Cancer of unknown primary (CUP) rarely originates in the mediastinum and is even less common as a second malignancy following a prior CUP resection. A 61-year-old man with no prior malignancy was diagnosed with an anterior mediastinal tumor, resected and identified as metastatic squamous cell carcinoma of unknown primary originating in a lymph node. Eighteen months later, during pneumonia treatment, a computed tomography (CT) scan revealed enlarged lower paratracheal lymph nodes. Initial biopsy showed no malignancy, and the lymph nodes remained stable for 20 months. Over the next year, these nodes progressively enlarged, extending to the subcarinal and left hilar lymph nodes. A transbronchial biopsy confirmed the subcarinal lesion as a poorly differentiated adenocarcinoma, distinct from the initial cancer. A comprehensive systemic workup failed to identify a primary site, leading to a second CUP diagnosis. Due to chronic respiratory failure from underlying lung disease, the patient was ineligible for cancer treatment. One year after the second CUP diagnosis, a CT scan detected a mass in the right lower lobe, which grew over the following year, as confirmed by a follow-up CT scan, suggesting a hidden lung cancer that emerged later. The patient passed away 75 months after the first cancer surgery and 24 months after the second CUP diagnosis, two weeks after the final scan, without an autopsy. This case highlights the rare occurrence of sequential, histologically distinct CUPs - likely represents the first reported instance - and the diagnostic challenges in identifying primary cancer sites, compounded by the patient's comorbidities precluding treatment.
原发灶不明的癌症(CUP)很少起源于纵隔,作为先前CUP切除术后的第二原发性恶性肿瘤则更为罕见。一名61岁无既往恶性肿瘤病史的男性被诊断为前纵隔肿瘤,经切除后被确定为起源于淋巴结的原发灶不明的转移性鳞状细胞癌。18个月后,在肺炎治疗期间,计算机断层扫描(CT)显示气管旁下淋巴结肿大。初次活检未发现恶性肿瘤,这些淋巴结在20个月内保持稳定。在接下来的一年里,这些淋巴结逐渐增大,延伸至隆突下和左肺门淋巴结。经支气管活检证实隆突下病变为低分化腺癌,与最初的癌症不同。全面的全身检查未能确定原发部位,导致第二次CUP诊断。由于潜在肺部疾病导致的慢性呼吸衰竭,该患者不符合癌症治疗条件。第二次CUP诊断一年后,CT扫描在右下叶发现一个肿块,在随后的一年里持续增大,后续CT扫描证实了这一点,提示后来出现了隐匿性肺癌。患者在首次癌症手术后75个月、第二次CUP诊断后24个月,即最后一次扫描两周后去世,未进行尸检。该病例突出了罕见的序贯性、组织学上不同的CUP的发生——可能是首例报道——以及在识别原发癌部位时面临的诊断挑战,患者的合并症使治疗更加复杂。