Feizi Iraj, Sedigh-Namin Atabak, Kani AmirAbbas, Namin Sonia Sharifi, Toularoud Alireza Bagheri
Department of Surgery, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Students Research Committee, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran.
Int J Surg Case Rep. 2025 May;130:111305. doi: 10.1016/j.ijscr.2025.111305. Epub 2025 Apr 14.
Multiple primary malignancies (MPMTs), the occurrence of two or more different primary cancers in a single person, are rare. These tumors can be synchronous or metachronous, with an incidence ranging from 0.73 % to 11.70 % in cancer patients. While invasive ductal carcinoma (IDC) is the most common form of breast cancer and lung neuroendocrine tumors (NETs) are rare, their co-occurrence as MPMT is extremely rare. In addition, chronic myeloid leukemia (CML) makes such cases even more complex.
We report the case of a 59-year-old woman who presented with a lump in the left breast. Diagnostic examinations confirmed breast IDC. Metastatic examination identified a separate primary, well-differentiated NET of the left lung. Both malignancies were treated surgically followed by appropriate adjuvant therapy. A year later, routine follow-up revealed an elevated white blood cell count and a subsequent bone marrow biopsy confirmed the diagnosis of CML.
The diagnosis of IDC and pulmonary NET as primary tumors is rare and the subsequent development of CML in this setting has not been reported previously. This case highlights the critical importance of thorough diagnostic evaluations to accurately differentiate between metastatic disease and MPMTs. The occurrence of three different malignancies in a single patient presents significant treatment challenges and highlights the need for personalized treatment approaches.
This report emphasizes the need for comprehensive diagnostic protocols in the evaluation of multiple tumors and contributes to the growing body of knowledge about MPMT. The coexistence of IDC, pulmonary NET and subsequent CML represents a rare and complex clinical scenario that requires continuous research into optimal management strategies for such cases.
多原发性恶性肿瘤(MPMTs)指的是在同一个人身上出现两种或更多不同的原发性癌症,这种情况较为罕见。这些肿瘤可以是同时发生的,也可以是异时发生的,在癌症患者中的发病率为0.73%至11.70%。虽然浸润性导管癌(IDC)是乳腺癌最常见的形式,而肺神经内分泌肿瘤(NETs)较为罕见,但它们作为MPMT同时出现的情况极为罕见。此外,慢性髓性白血病(CML)使此类病例更加复杂。
我们报告了一名59岁女性的病例,她因左侧乳房出现肿块就诊。诊断检查确诊为乳腺IDC。转移灶检查发现了一个独立的、分化良好的左肺原发性NET。两种恶性肿瘤均接受了手术治疗,随后进行了适当的辅助治疗。一年后,常规随访显示白细胞计数升高,随后的骨髓活检确诊为CML。
将IDC和肺NET诊断为原发性肿瘤的情况罕见,且此前尚未报道过在此情况下随后发生CML的病例。该病例凸显了进行全面诊断评估以准确区分转移性疾病和MPMTs的至关重要性。单一患者出现三种不同的恶性肿瘤带来了重大的治疗挑战,并凸显了个性化治疗方法的必要性。
本报告强调了在评估多种肿瘤时需要全面的诊断方案,并为有关MPMT的知识体系不断发展做出了贡献。IDC、肺NET和随后的CML共存代表了一种罕见且复杂的临床情况,需要对这类病例的最佳管理策略进行持续研究。