The gastrointestinal tract is the most common extranodal site affected by NHL, accounting for about 50–60% of all extranodal cases[2], whereas the stomach is the most common gastrointestinal site (60–75%)[3]. Patients with NHL have a higher rate of secondary malignancy than the general population, and lung cancer is the most common type[4, 5], chemotherapy such as CHOP or CHOP-like regimen and radiotherapy should be accounted for it[1, 6, 7]. However, coexistence of primary lymphoma and primary lung cancer has rarely been reported. After an extensive literature search, only eleven other published cases were identified [8–18] (Table 1).
Table 1
Synchronous malignant lymphoma and lung cancer in the literature
Year/ref. | Age /gender | Lung cancer | Malignant lymphoma | Treatment | Outcome | Survival time (months) |
1999/[8] | 71/F | SCC | TCL/lung | lobectomy + chemotherapy(CHOP) | died of progression of lymphoma | 7 |
2000/[9] | 67/M | SCC | MALToma/lung | lobectomy + chemotherapy (THP-COP) | died of pulmonary fibrosis due to chemotherapy | 11 |
2001/[10] | 74/M | Adenoca | MALToma/lung | lobectomy | alive | 12 |
2002/[11] | 67/M | SCC | MALToma/lung | lobectomy + chemotherapy (CHOP + carboplastin plus taxol) | alive | 6 |
2008/[12] | 73/M | Adenoca | MCL/pleura | chemotherapy Endoxan + Farmorubicin + Vincristine) | alive | 14 |
2008/[13] | 74/M | Adenoca | MALToma/lung | lobectomy, NHL was left untreated | N/A | N/A |
2012/[14] | 60/F | Adenoca | MALToma/lung | lobectomy, NHL was left untreated | N/A | N/A |
2017/[15] | 45/M | Adenoca | MCL/lung | 6 cures of alternating RCHOP and RDHAP (dexamethasone, high-dose Ara-Cytarabine and cisplatin) + autologous stem cell transplantation. | died of treatment complications | 36 |
2020/[16] | 69/F | Adenoca | MALToma/lung | lobectomy + chemotherapy (CHOP) | alive | 12 |
2020/[17] | 64/M | SCC | MALToma/lung | N/A | N/A | N/A |
2021/(The current case) | 75/M | Adenoca | DLBCL/stomach | RFA + chemotherapy(R-CHOP) + Radioactive seed implantation | alive | 27 |
2023/[18] | 63/M | SCC | MALToma/lung | surgical resection | alive | N/A |
SCC: squamous cell carcinoma; Adenoca: Adenocarcinoma; TCL: T-cell lymphoma; MALToma: Mucosa-associated lymphoid tissue lymphoma; MCL: Mantle cell lymphoma; DLBCL: diffuse large B-cell lymphoma; THP-COP: cyclophosphamide, pirarubicin, vincristine, and prednisolone; |
As presented in Table 1, all the twelve cases, including our case, were older than 45 years with a mean age of 66.8 years, and nine of them were men. All these cases suffered from non-small-cell lung cancer (NSCLC), and the most common type of lymphoma was mucosa-associated lymphoid tissue type (eight cases). The present case could be the first case of synchronous gastric lymphoma and lung cancer. Although the exact etiology of synchronous gastric lymphoma and lung cancer remains unknown, some scholars speculated that common predisposing factors, including smoking, Helicobacter pylori (H. pylori) infection, and genomic alternations, may play a role[9, 10, 13]. For the present case, however, the patient never smoked and was negative for H. pylori infection. In addition, the patient’s chromosome karyotype was normal, and no gene mutations other than EGFR were identified. Thus, whether the two primary malignancies observed in the present case were correlated or whether they were the result of independent events could not be confirmed.
Reviewing the eleven reported cases, the treatment protocols varied from observation to surgery, chemotherapy or in combination; however, the best treatment option remains controversial. Therefore, an individualized management is necessary. The present case is an old man who could not tolerate two entirely different types of chemotherapy, whereas R-CHOP regimen is the best choice for NHL; thus, the two lung cancer lesions were locally treated and managed first. CT-guided RFA was selected as it is an effective and minimally invasive treatment for medically inoperable NSCLC[19]. However, the left lung adenocarcinoma was not suitable for RFA; therefore, radioactive particle implantation was opted instead. Another key point to consider is prophylactic antifungal treatment before and during chemotherapy as the mortality of disseminated cryptococcosis after the R-CHOP regimen has been reported to be as high as 54%[20, 21]. After undergoing a series of treatment, the patient was finally discharged from our hospital with complete remission of gastric lymphoma and stable remission of lung adenocarcinoma; pulmonary cryptococcosis was also successfully treated.
In conclusion, synchronous primary diffuse large B-cell gastric lymphoma and bilateral primary lung adenocarcinoma is extremely rare, with the present case being the only one reported. This case highlights the need for proper staging and investigation of questionable findings before developing a patient’s treatment plan. The good clinical condition of the patient and CT scan results during the clinical follow-up indicated that the treatment was successful; however, the most suitable treatment protocol still needs to be identified on a case-by-case basis.