Double primary non-small cell lung cancer with synchronous small cell lung cancer N2 nodes: a case report

Abstract

Synchronous multiple primary lung cancer (SMPLC) is rare and very hard to distinguish from metastatic disease. Recent studies indicate the presence of this entity in the lung, with no mention to the involvement of the mediastinum. An extremely rare case of a 68-year-old male with double primary non-small cell lung cancer (NSCLC) in the left upper lobe and N2 positive nodes for small cell lung cancer (SCLC) is presented. Modern diagnostic criteria as well as aggressive curative strategies are encouraged, in order to achieve better survival rates for such patients.

Introduction

Synchronous multiple primary lung cancer (SMPLC) is a rare entity with an incidence of 1.5-2% per patient per year (1). The first diagnostic criteria for patients with SMPLC were established by Martini et al. in 1975 (2), and were refined by Antakli et al. in 1995 (3). However, not all patients with SMPLC match the above criteria (2). Involvement of the mediastinum is, surprisingly, excluded from these reports, leaving a vast gap in the staging and therapeutic strategy of such patients. The rise of modern diagnostic and imaging methods in addition to new curative and histological techniques are generally encouraged, with the hope of providing better survival rates, as reported recently (4-6).

Case presentation

A 68-year-old male patient, with Eastern Cooperative Oncology Group (ECOG) score 0-1, was referred to our clinic for surgical resection of a left upper lobe mass. A CT-guided biopsy of the tumor was performed a few days earlier, which revealed squamous cell carcinoma.

His medical history consisted of heavy smoking (110 PY) and hypertension. Chest-CT with 5 mm-thick images indicated a 4.3 cm diameter mass in the left upper lobe (Figure 1). No pathological lymph nodes of the mediastinum were described, and complete CT scan was negative for distant metastases. Laboratory findings were within normal limits. The spirometry results were quite satisfactory [forced expiratory volume in 1 second (FEV₁): 1.78-64%, forced vital capacity (FVC): 2.6-73%].

Figure 1.

Chest CT showing the 4.3 cm tumor in the left upper lobe, mediastinal and lung windows respectively.

An open left posterolateral thoracotomy was performed, with left upper lobectomy and mediastinal lymph node dissection from stations 5, 6, 9 and 10. The patient was hospitalized in the intensive care unit (ICU) of our hospital for the first 24 hours past fully conscious surgery. His post-operative recovery was uneventful and was discharged on the 8^th post-operative day.

Pathologic examination of the left upper lobe revealed two lesions; tumor 1, measured 6 cm in size, was confirmed to be a squamous cell carcinoma with low differentiation; tumor 2, 1 cm away from the first tumor, measured 0.5 cm in size, was identified as adenosquamous carcinoma with moderate differentiation. Immunohistochemical staining for tumor 1 showed strong positivity for cytokeratin (CK) 5/6 and p63 (Figure 2A), focal positivity for CK 7, while it was negative for thyroid transcription factor-1 (TTF-1), CK 20, chromogranin and synaptophysin. Tumor 2 matched the morphological characteristics of squamous carcinoma along with those of adenocarcinoma at about 10% (Figure 2B). Subaortic and aortopulmonary window lymph nodes were positive for small cell lung cancer (SCLC) (Figure 2C). Immunohistochemical staining was positive for low molecular weight CK, CK 7, chromogranin, CD56, p63 and TTF-1 (Figure 2D), weakly positive for synaptophysin and CK 5/6, while ki-67 was positive in almost 100% of the neoplasmatic cells. Pulmonary ligament and hilar lymph nodes were negative for metastasis. It is worth mentioning that the entire lobe was examined thoroughly under microscopic observation to exclude any potential SCLC component.

Figure 2.

Histology figures. (A) Squamous cell carcinoma, P63 immunostaining, original magnification ×20; (B) adenosquamous carcinoma, H-E stain, Presence of neoplastic glands and squamous cell nests, original magnification ×20; (C) small cell lung cancer (SCLC), H-E stain, fibrous tissue infiltrated by SCLC, original magnification ×20; (D) SCLC, thyroid transcription factor-1 (TTF-1) immunostaining, original magnification ×40.

The Thoracic Oncology Board of our hospital discussed the patient’s case, in order to determine the therapeutic plan that should be followed. Concurrent chemotherapy for SCLC with mediastinal radiation was decided. The patient started chemotherapy, with a plan of cisplatin 80 mg/m² IV on day 1, plus etoposide 100 mg/m² IV on days 1-3 every 28 days for 4 cycles, while radiation started along with cycle 2 of chemotherapy.

Discussion

Multiple primary lung cancers (MPLCs) can be either synchronous, or metachronous (6). Synchronous MPLC refer to two or more neoplasms that develop independently during the same period, without the involvement of common lymphatics (2). SMPLCs represent 19.6-40% of multiple lung cancer (MLC) patients, while 48.7% of patients with SMPLC have different histologic types. Whatever the type of SMPLC though, reports indicate that the 5-year survival rates are not correlated with similar or different histologic classification (6). Squamous cell carcinoma is the most common type of lung cancer, comprising over 70% of SMPLCs (7).

Generally accepted diagnostic criteria have been established, which include both imaging and pathological characteristics (2,3). However, the proposed criteria are not always sufficient, as SMPLCs are revealed more frequently, causing difficulties in determining the etiology of multiple malignant lung lesions. Modern imaging methods may provide valuable clues for preoperative distinction of SMP LCs from metastatic disease (2,8).

According to current reports, aggressive curative approach is the preferred strategy in dealing with SMPLCs, leading to an increase in overall survival, with 5-year rates up to 38% (5,9,10). Surgical procedures depend on the stage, the location of the tumors, and the patients’ performance status (5,10). Stereotactic radiotherapy and chemotherapy are also suggested to provide an added survival advantage (4,11).

Immunohistochemistry is the key in identifying such tumors, when preoperative diagnosis fails to contribute. Should it prove correct, a more detailed differentiation by the pathologist, using modern techniques, such as DNA studies or the p53 gene mutation, would be of great importance in the diagnosis and treatment of SMPLCs (6).

In the current study, we present the case of a 68-year-old male patient who was referred to our clinic for excision of a left upper lobe tumor, but histology revealed three different types of lung cancer (squamous, adenosquamous and SCLC). This study comes to underline the rarity of such cases, as well as the complexity of the treatment strategy that should be followed. Moreover, despite the fact that the two tumors of the excised lobe met the criteria for SMPLC, the positivity of the lymph nodes for SCLC arises questions, as no current study or guidelines exist for the treatment protocol of such cases.

In conclusion, it is quite difficult to distinguish a SMPLC from intrapulmonary metastases originating from a single pulmonary neoplasm or other neoplasms in different organs (2). Recent advances in imaging, along with careful clinical assessment can offer a valuable tool in the evaluation of SMPLCs and metastatic lesions. Therefore, we agree with Detterbeck et al. (1) that experienced multidisciplinary teams must define SMPLCs, judging and considering all information given.