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27 December 2014: Articles  Japan

A Case of Synchronous Double Primary Lung Cancer Presenting with Pleomorphic Carcinoma and Adenocarcinoma

Rare disease, Rare coexistence of disease or pathology

Naohiro Taira AE , Tsutomu Kawabata C , Takaharu Ichi F , Kazuaki Kushi B , Tomofumi Yohena DF , Hidenori Kawasaki C , Kiyoshi Ishikawa CD , Seiya Kato B

DOI: 10.12659/AJCR.892339

Am J Case Rep 2014; 15:576-579

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Abstract

BACKGROUND: Recently, synchronous multiple lung cancer (SMPLC) has sometimes been detected as a result of improved radiological imaging, although the occurrence of SPMLC is still rare. To the best of our knowledge, there have been no reported cases of with synchronous double primary lung cancer presenting with pleomorphic carcinoma and adenocarcinoma. We herein report such a case.

CASE REPORT: A 64-year-old male was referred to our institution for an abnormal shadow in the apex of the left lung in April 2012. CT revealed 2 nodules that measured 15 mm in the left S1+2b and 20 mm in the left S3c. We suspected that the lesions were malignant, although the diagnosis could not be confirmed by transbronchial lung biopsy of the lesions. Therefore, we performed the left upper lobectomy. The results of the pathological examination of the nodule in S3c showed adenocarcinoma of pT1aN0M0, stage IA. The nodule in S1+2b was found to be pleomorphic carcinoma, pT1aN0M0, stage IA. In November 2012, the patient underwent an esophagogastroduodenoscopy because of anemia. The image findings showed a gastric ulcer on the greater curvature of his stomach. The pathological examination of the biopsy specimen from the ulcer revealed the metastatic cancer from pleomorphic carcinoma. In addition, abdominal CT revealed bilateral adrenal metastasis. Although the patient received chemotherapy, it was not effective. It was difficult to continue the chemotherapy because his performance status worsened. He died in May 2013.

CONCLUSIONS: The present case was associated with a poor prognosis, even though the pathological stage of each tumor was stage IA. The prognosis of SMPLC may be associated with the histologic type, although the prognosis of SMPLC remains unclear due to its rarity.

Keywords: Fatal Outcome, Adenocarcinoma - therapy, Lung Neoplasms - therapy, Neoplasms, Multiple Primary - therapy

Background

Recently, synchronous multiple lung cancer (SMPLC) has sometimes been detected due to improvements in radiological imaging. The original criteria for multiple lung cancers were first reported in 1932 by Warren and Gates [1], who stated each tumor must represent a definite picture of carcinoma, each tumor must be distinct, and that the probability of 1 lesion metastasizing from another must be excluded. In addition, Martini and Melamed [2] indicated that SMPLC requires the existence of tumors in different portions of an organ and different histological types, or the existence in a different lobe or segment.

The occurrence of squamous cell carcinoma with squamous cell carcinoma has been the most frequent type of synchronous double lung cancer [3,4]. To the best of our knowledge, there have been no reported cases dealing with synchronous double primary lung cancer presenting with pleomorphic carcinoma and adenocarcinoma. We herein report such a case.

Case Report

A 64-year-old male was referred to our institution for evaluation of an abnormal shadow on a chest X-ray in April 2012. He had been healthy with no symptoms and had an unremarkable medical and family history, and was a current smoker. The chest X-ray showed an abnormal shadow in the apex of the left lung (Figure 1). Contrast-enhanced CT revealed a nodule with an irregular margin that measured 15 mm in the left S1+2b (Figure 2A). In addition, the image showed another nodule that measured 20 mm in the left S3c (Figure 2B). Enlarged lymph nodes were not detected in the mediastinum. The levels of serum tumor markers such as CEA, CYFLA and ProGRP were within normal ranges. There were no other signs of distant metastasis based on a CT scan of the chest, abdomen, and pelvis, or by brain MRI.

We suspected that the lesions were primary lung cancers, although the diagnosis could not be confirmed by transbronchial lung biopsy. In May 2012, we performed left upper lobectomy, and a pathological diagnosis of lung cancer was confirmed based on the results of a flash-frozen section biopsy of the nodule in the left S3c, although the biopsy of the nodule in the left S1+2b showed necrotic cells and no malignant cells. There were no intraoperative complications, and the patient had an uneventful recovery. The final results of the pathological examination of the nodule in the left S3c showed adenocarcinoma of pT1aN0M0, stage IA. The nodule in the left S1+2b was diagnosed as pleomorphic carcinoma, pT1aN0M0, stage IA (Figure 3). There was no lymphovascular invasion by either lesion.

The patient received regular follow-up without adjuvant chemotherapy. In November 2012, 6 months after the left upper lobectomy, the patient began having mild anemia, with hemoglobin values as low as 8.4 g/dL, although he had a baseline hemoglobin concentration of approximately 13 g/dL. He received a transfusion of packed red cells and underwent esophagogastroduodenoscopy (EGD) and a colonoscopy as work-up for the anemia. The EGD showed a gastric ulcer on the greater curvature of his stomach (Figure 4). The pathological examination of the biopsy specimen of the ulcer revealed metastatic cancer from pleomorphic carcinoma. Besides the gastric metastasis, abdominal CT revealed bilateral adrenal metastasis.

The patient received chemotherapy with carboplatin and pemetrexed, but it was not effective. Furthermore, it was difficult to continue the chemotherapy because his performance status worsened. He died on May 2013.

Discussion

The occurrence of SPMLC is rare, and the incidence of synchronous multiple primary lung cancers ranges from 1% to 7% according to clinical trials [2]. Among these cases, those of the bilateral type comprise 60–70%, while the unilateral type is been comparatively rare [5,6]. With regard to the histological types of SPMLC, the occurrence of squamous cell carcinoma and squamous cell carcinoma has been the most common, followed by squamous cell carcinoma and small cell carcinoma, and squamous cell carcinoma and adenocarcinoma [3,7].

The prognosis of SMPLC remains unclear. Whereas the overall survival rate (OS) of patients diagnosed with SMPLC had been reported to be significantly lower than in patients with single primary lung cancers (SPLC) [8], Yu et al. reported that there was no significant difference in OS between SPMLC and SPLC [9]. While tumor size is thought to an important predictor of OS in SMPLC [9,10], the presence of lymphovascular invasion and the histology of SMPLC do not significantly affect OS according to Yu et al. [11,12]. However, the present case was associated with a very poor prognosis, despite the fact that the T stage of each tumor was T1a. This may be associated with the histology of 1 of the tumors, which was pleomorphic carcinoma, because the pathological examination of the gastric ulcer confirmed metastasis of the lung pleomorphic carcinoma, and the other metastasis was also thought to have originated from pleomorphic carcinoma.

Pleomorphic carcinoma of the lung is rare, accounting for 0.3% to 1% of all lung malignancies [13]. Pleomorphic carcinoma was first classified as a carcinoma with pleomorphic, sarcomatoid, or sarcomatous elements by the World Health Organization in 1999, and in the 2003 Classification of Lung Cancers was defined as a poorly differentiated non-small cell carcinoma, which includes squamous cell carcinoma, adenocarcinoma, and large-cell carcinoma that contains spindle cells or giant cells, and cancers that contain at least 10% spindle cells or giant cell areas [14].

Pulmonary pleomorphic carcinoma was associated with a poor prognosis in previous studies, even when early-stage disease was diagnosed and resected [15]. In addition, pulmonary pleomorphic carcinoma showed a poor response to chemotherapy [16]. The prognosis of affected patients is generally poorer than that of patients with other types of non-small cell lung cancer [17]. These previous findings of pulmonary pleomorphic carcinoma were also noted in our present case.

Conclusions

In conclusion, the prognosis of SMPLC may be associated with the histological type. To the best of our knowledge, there have been no reported cases dealing with synchronous double primary lung cancer presenting with pleomorphic carcinoma and adeno-carcinoma. Therefore, more thorough scientific documentation is needed on survival of SMPLC cases with pleomorphic carcinoma.

Reference:

1.. Warren S, Gates O, Multiple primary malignant tumors: a survey of the literature and a statistical study: Am J Cancer, 1932; 16; 1358-414

2.. Martini N, Melamed MR, Multiple primary lung cancers: J Thorac Cardiovasc Surg, 1975; 70; 606-12, pmid: 170482

3.. Rohwedder JJ, Weatherbee L, Multiple primary bronchogenic carcinoma with a review of the literature: Am Rev Respir Dis, 1974; 109; 435-45, pmid: 4361387

4.. Ferguson MK, DeMeester TR, DeLauriers J, Diagnosis and management of synchronous lung cancers: J Thorac Cardiovasc Surg, 1985; 89; 378-85, pmid: 3974273

5.. Morita T, [Incidence, contents and change of autopsied multiple primary cancers of the lung based on the annual of the autopsy cases in Japan between 1958 and 1992.]: Haigan, 1997; 37; 283-94 [in Japanese]

6.. Matsuge S, Hosokawa Y, Sato K, [Surgical treatment for bilateral multiple lung cancers.]: Kyobu Geka, 2000; 53; 89-95, pmid: 10667015 [in Japanese]

7.. Kobashi Y, Fukuda M, Yoshida K, Synchronus Presentation of Early-stage Small Cell Carcinoma and Adenocarcinoma in the Same Lung Lobe: Intern Med, 2006; 45; 287-91, pmid: 16595996

8.. Ferguson MK, DeMeester TR, DeLauriers J, Diagnosis and management of synchronous lung cancers: J Thorac Cardiovasc Surg, 1985; 89; 378-85, pmid: 3974273

9.. Yu YC, Hsu PK, Yeh YC, Surgical Results of Synchronous Multiple Primary Lung Cancers: Similar to the Stage-Matched Solitary Primary Lung Cancers?: Ann Thorac Surg, 2013; 96; 1966-74, pmid: 24021769

10.. Antakli T, Schaefer RF, Rutherford JE, Read RC, Second primary lung cancer: Ann Thorac Surg, 1995; 59(4); 863-66, pmid: 7695410 discussion 867

11.. Rostad H, Strand TE, Naalsund A, Norstein J, Resected synchronous primary malignant lung tumors: a population- based study: Ann Thorac Surg, 2008; 85; 204-9, pmid: 18154811

12.. Voltolini L, Rapicetta C, Luzzi L, Surgical treatment of synchronous multiple lung cancer located in a different lobe or lung: high survival in node-negative subgroup: Eur J Cardiothorac Surg, 2010; 37; 1198-204, pmid: 20022516

13.. Rossi G, Cavazaa A, Sturm N, Pulmonary carcinomas with pleomorphic, sarcomatoid, or sarcomatous element: a clinicopathologic and immunohistochemical study of 75 cases: Am J Surg Pathol, 2003; 27; 311-24, pmid: 12604887

14.. : General rule for clinical and pathological record of lung cancer, 2003; 128-29, Tokyo, Kanehara Shuppan [in Japanese]

15.. Yuki T, Sakuma T, Ohbayashi C, Pleomorphic carcinoma of the lung: a surgical outcome: J Thorac Cardiovasc Surg, 2007; 134(2); 399-404, pmid: 17662779

16.. Bae HM, Min HS, Lee SH, Palliative chemotherapy for pulmonary pleomorphic carcinoma: Lung Cancer, 2007; 58(1); 112-15, pmid: 17574296

17.. Mochizuki T, Ishii G, Nagai K, Pleomorphic carcinoma of the lung: clinicopathologic characteristics of 70 cases: Am J Surg Pathol, 2008; 32; 1727-35, pmid: 18769330

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923