Case 2– A 66-year-old male patient with coronary artery pathology was admitted to our facility, and during his evaluation, a lesion in the upper lobe of the right lung that showed malignant characteristics was detected. Eventually, the patient underwent coronary artery bypass grafting (CABG) and pulmonary resection simultaneously, and a histopathological examination revealed an adenocarcinoma of the lung (Figure 2a). Five years later, the patient was diagnosed with prostate adenocarcinoma and had a prostatectomy. Two years after this operation, a lesion on the skin of the right side of his nose appeared, which was then excised and diagnosed as basal cell carcinoma of the skin. Five years after his last surgery, the patient was readmitted to our clinic with a 6 cm lesion with malignant features in the left paracardiac region adjacent to the mediastinum (Figure 2b). Systemic screening revealed no metastasis, and the mass was completely removed and identified as a malignant solitary fibrous tumor demonstrating excessive mitosis. The patient remained free of disease during a six-month follow-up period.
Although it has been postulated that the incidence of MPMs increase in correlation with increased elderly population, other reasons such as the long-time survival of malignancies and the immunostimulating effect of previous cancer also likely may play a part.[3] Both of our cases were diagnosed and treated at an age which puts them in the “old” category.
Genetic, hormonal, environmental, and immunological factors may play a role in the etiology of MPMs,[1] and Keller et al.[4] showed that the most important factors responsible for these malignancies are genetic predisposition and chromosomal aberrations. In addition, during the follow-up of certain types of malignancies, development of a tumor in a secondary organ is possible, but this depends on the effect of the exposure to carcinogenic agents.[5] Unfortunately, we did not investigate this aspect in our patients.
As our two cases and the review by Koutsopoulos et al.[6] point out, MPMs can be seen synchronously. Our cases were diagnosed with three and four different malignancies, respectively, and to the best of our knowledge, no cases like these have been previously reported in the literature.
Declaration of conflicting interests
The authors declared no conflicts of interest with
respect to the authorship and/or publication of this
article.
Funding
The authors received no financial support for the
research and/or authorship of this article.
1) Kılcıksız SC, Kaynak C, Eski E, Yersal O, Unlu I, Callı A, et
al. Evaluation of multiple primary tumors and single tumors
characteristics: a study from hospital-based cancer registry in
Izmir. TJ Oncol 2007;22:55-62.
2) Demandante CG, Troyer DA, Miles TP. Multiple primary
malignant neoplasms: case report and a comprehensive
review of the literature. Am J Clin Oncol 2003;26:79-83.
3) Balducci L, Beghe’ C. Cancer and age in the USA. Crit Rev
Oncol Hematol 2001;37:137-45.
4) Keller U, Grabenbauer G, Kuechler A, Sprung CN, Müller
E, Sauer R, et al. Cytogenetic instability in young patients
with multiple primary cancers. Cancer Genet Cytogenet
2005;157:25-32.