Adult Chest Surgery

Chapter 9. Role of the Pathologist 

 

A pathologist experienced in thoracic oncology is an essential member of the thoracic team. Surgical resection related to lung cancer and other pulmonary pathology accounts for the largest proportion of current thoracic practice. The goals of pathologic analysis of surgical lung specimens are to classify the lung cancer, determine the extent of its invasion (i.e., pleural, lymphovascular, soft tissue, or chest wall), and establish the status of the surgical margins for cancer involvement.Accurate disease identification and staging are of pinnacle importance to the decision-making process and influence the diagnosis (benign or malignant), course of treatment, selection of optimal surgical approach, and pursuit of appropriate adjuvant and neoadjuvant therapies such as chemotherapy, radiation, and other innovative approaches to treatment.

After a malignancy has been identified, the pathologist must determine whether the tumor is primary versus metastatic. Most tumors found in the lung represent metastatic foci from distant primaries, such as breast and colon cancer, as opposed to a primary lung malignancy. While the pathologic features of metastatic versus primary adenocarcinoma may be similar, for example, the treatment course is not. Immunohistochemistry is required to make the distinction and has proved to be an invaluable diagnostic adjunct. Primary malignant tumors of the lung are most often of epithelial or mesenchymal origin. The epithelial tumors are broadly divided into small cell lung cancer (SCLC) and non–small cell lung cancer (NSCLC). NSCLC is further classified as squamous cell carcinoma, adenocarcinoma, and large cell carcinoma (LCC).2

The pathologist plays a fundamental role in the preoperative, intraoperative, and postoperative evaluation. The preoperative evaluation includes examination of one of the following specimens: bronchial brushings, bronchial washings, fine-needle aspiration biopsy, core needle biopsy, endobronchial biopsy, and transbronchial biopsy. Because lung tumors demonstrate a great deal of heterogeneity, accurate classification depends on sampling technique: If the pathology sample is limited, sometimes the only categorization that can be made is the distinction between NSCLC and SCLC. Lymph node status is one of the most important prognostic features in patients with NSCLC.3,4 Since mediastinoscopy with pathologic examination of lymph nodes remains the "gold standard" for the evaluation of lymph node status in patients with NSCLC, mediastinal lymph nodes are sampled during the preoperative evaluation and provide information important to staging and therapeutic options.5–8

The intraoperative evaluation of the surgical pathology specimen is performed by frozen-section examination, which can be analyzed immediately, and findings are communicated to the operating room. Lobectomy or pneumonectomy specimens are routinely evaluated intraoperatively to determine the status of the surgical resection margin, to diagnose incidental nodules discovered at the time of surgery, and to evaluate regional lymph nodes.

The postoperative evaluation reveals pathologic characteristics necessary for classification of tumor type, staging, and prognostic factors. The parameters considered in the surgical pathology report are histologic type, histopathologic grade, visceral pleural invasion (Fig. 9-1), venous/lymphatic vessel invasion (Fig. 9-2), and extracapsular extension of positive mediastinal lymph nodes, TNM stage, and stage grouping.9

Figure 9-1.

 
 

Lung adenocarcinoma with invasion of visceral pleura. A. Photomicrograph from a lobectomy specimen removed for adenocarcinoma. Tumor cells are invading into the parenchyma and are in the vicinity of the pleura but do not appear to cross over (H&E stain, x200). B. However, an elastic stain highlights the elastic lamina of the visceral pleura (arrows) clearly being transected by tumor (elastic Verhoeff stain, x200).

 

Figure 9-2.

 

Lymphovascular invasion. Photomicrograph from a lobectomy specimen removed for adenocarcinoma illustrating a cluster of tumor cells present in a vascular space, away from the main tumor mass (H&E stain, x200).

The World Health Organization's (WHO) pathologic classification of lung tumors was revised in 1999, 18 years after the previous edition. The 1999 revision contained numerous changes and revisions to account for the vast progress in lung cancer research in the preceding 18 years.10 This tumor classification system provides the foundation for tumor diagnosis and patient therapy and a critical basis for epidemiologic and clinical studies.11 The most important changes in the 1999 revised classification system were (1) clarification of the preinvasive lesions in lung neoplasia, (2) reclassification of adenocarcinoma, (3) addition of two new entities to the category of large cell neuroendocrine carcinoma (LCNEC), and (4) addition of a new category called pleomorphic carcinoma.

In the revised WHO classification system, (1) lesions attributed to preinvasive lung cancer included squamous dysplasia, atypical adenomatous hyperplasia, and diffuse idiopathic pulmonary neuroendocrine cell hyperplasia; (2) the definition of bronchioloalveolar carcinoma (BAC) was restricted to noninvasive tumors; (3) two new entities, both with unfavorable prognoses, were added to the category of large cell carcinoma, that is, LCNEC and basaloid carcinoma; and (4) pleomorphic carcinoma was defined as a group of poorly differentiated non–small cell carcinomas with heterogeneous elements, such as spindle cells and/or giant cells. Carcinosarcoma and pulmonary blastoma also were included in this category.

Extensive sampling is necessary to correctly identify each of these elements of the surgical pathology specimen. In 2004, a revised WHO classification was created after a consensus meeting in Lyon, France. The 2004 modification retains much of the same nomenclature as the 1999 edition and maintains the same major diagnostic groups.2,12 The surgical pathology report always should include the histologic classification published by the WHO for carcinomas of the lung13 (Table 9-1).

Table 9-1. World Health Organization Classification of Lung Neoplasms

Epithelial tumors*

Soft tissue tumors

Mesothelial tumors

Miscellaneous tumors

Lymphoproliferative diseases

Secondary tumors (metastatic)

Unclassified tumors

Tumor-like lesions

Preinvasive lesions

  Squamous dysplasia

  Atypical adenomatous hyperplasia

  Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia

Malignant epithelial tumors of the lung:

  Squamous cell carcinoma

     Variants

        Papillary

        Clear cell

        Small cell

        Basaloid

  Small cell carcinoma

     Variant: Combined small cell carcinoma (small cell carcinoma and non–small cell component)

Adenocarcinoma

  Adenocarcinoma, mixed subtype

  Acinar

  Papillary

  Bronchioloalveolar carcinoma

     Nonmucinous

     Mucinous

     Mixed mucinous and nonmucinous type

  Solid adenocarcinoma with mucin production

     Variants

        Fetal adenocarcinoma

        Mucinous ("colloid") adenocarcinoma

        Mucinous cystadenocarcinoma

  Signet-ring adenocarcinoma

Clear cell adenocarcinoma

Large cell carcinoma

  Variants

     Large cell neuroendocrine carcinoma

     Combined large cell neuroendocrine carcinoma

     Basaloid carcinoma

     Lymphoepithelioma-like carcinoma

     Clear cell carcinoma

     Large cell carcinoma with rhabdoid phenotype

Adenosquamous carcinoma

Sarcomatoid carcinoma

  Pleomorphic carcinoma

  Spindle cell carcinoma

  Giant cell carcinoma

  Carcinosarcoma

  Pulmonary blastoma

Carcinoid tumor

  Typical carcinoid

  Atypical carcinoid

Carcinomas of salivary gland type

  Mucoepidermoid carcinoma

  Adenoid cystic carcinoma

  Epithelial-myoepithelial carcinoma

Unclassified carcinoma

 

*Most of the lung neoplasms are malignant epithelial tumors.

BRONCHIOLOALVEOLAR CARCINOMA

BAC is an important subtype of pulmonary adenocarcinoma. This cancer has received increasing attention in recent years owing to its increasing incidence and rate of sensitivity to epidermal growth factor–tyrosine kinase inhibitors.14

Since 1999, the WHO classification has been more restrictive in the definition of BAC and includes only noninvasive tumors, where the neoplastic cells spread out along preexisting alveolar structures (lepidic spread).13 Pure BAC requires absence of invasion of stroma, pleura, or lymphatic spaces.11 Tumors that include some, but not all, of these features are classified as adenocarcinoma of mixed type with a predominant BAC pattern.15

BAC is divided into three subtypes: mucinous (Fig. 9-3), nonmucinous (Fig. 9-4), and a mixed mucinous and nonmucinous, or indeterminate, form.13 As with conventional lung adenocarcinoma, nonmucinous BAC expresses thyroid transcription factor 1 (TTF-1). Mucinous BACs, however, may have an aberrant immunophenotype: They express CK20 but reportedly lack TTF-1 and CK7 expression.16

Figure 9-3.

 

Mucinous bronchioloalveolar carcinoma. Respiratory alveoli are lined by malignant mucinous columnar cells arranged in a lepidic growth pattern. The alveolar architecture is preserved (H&E stain, x200).

 

Figure 9-4.

 

Nonmucinous bronchioloalveolar carcinoma. Uniform involvement of the alveolar walls by proliferation of cuboidal cells with severe atypia. The tumor cells have hyperchromatic nuclei with severe atypia protruding into the alveolar spaces in a hobnail growth pattern (H&E stain, x400).

Both subtypes of BAC should be distinguished morphologically from primary adenocarcinoma of the conventional type, metastatic adenocarcinoma, and other benign and/or reactive conditions. As with pulmonary adenocarcinoma of the conventional type, BACs are usually CK7+ and CK20– and therefore distinguishable from CK7– and CK20+ metastatic adenocarcinoma of the colorectum. However, mucinous BAC is often CK7+/CK20+.17 CDX-2, which is a highly sensitive and specific marker of adenocarcinomas of intestinal origin, helps to distinguish mucinous BAC from metastatic primary gastrointestinal cancers.

Tumors with Neuroendocrine Morphology

Neuroendocrine tumors of the lung are a distinctive subset of lung cancers characterized by varying degrees of neuroendocrine morphologic, immunohistochemical, and ultrastructural features.12 This category includes a wide spectrum of tumor types: low-grade typical carcinoid (TC) (Fig. 9-5), intermediate-grade atypical carcinoid (AC) (Fig. 9-6), and two high-grade tumors, LCNEC (Fig. 9-7) and SCLC (Fig. 9-8).18 Accurate classification of neuroendocrine tumors has prognostic importance. The grade of malignancy of neuroendocrine tumors progresses in the following order: TC, AC, LCNEC, and SCLC.18 No prognostic difference was noted between LCNEC and SCLC. The carcinoid nomenclature is preferred by the WHO over terms such as well-differentiated neuroendocrine carcinoma because it provides continuity with established terminology familiar to clinicians.13 In the 2004 WHO classification, TC and AC are categorized together under the heading of carcinoid tumors; LCNEC is listed as a subtype of LCC, and SCLC is retained as an independent category. Histologically, the neuroendocrine features consist of an organoid or trabecular growth pattern, peripheral palisading of tumor cells around the periphery of tumor nests, and the formation of rosette structures.

Figure 9-5.

 

Typical carcinoid tumor. This tumor demonstrates cells arranged in cords and tubules with a nesting pattern. The tumor cells have a moderate amount of eosinophilic cytoplasm and nuclei showing finely granular (salt and pepper) chromatin. No necrosis or mitoses are seen (H&E stain, x400).

 

Figure 9-6.

 

Atypical carcinoid tumor. This tumor is defined as a neuroendocrine tumor that meets one of the two criteria: 2–10 mitoses per 2 mm2 or necrosis. Although no mitoses were identified, necrosis was present focally (arrow). The tumor cells are atypical, have a moderate amount of eosinophilic cytoplasm, and have nuclei showing finely granular (salt and pepper) chromatin (H&E stain, x400).

 

Figure 9-7.

 

LCNEC is defined as a neuroendocrine tumor with greater than 10 mitoses per 2 mm2 (arrows) and cytologic features of large cell carcinoma. Cells have polygonal shape, abundant cytoplasm, and prominent nucleoli (H&E stain, x400).

 

Figure 9-8.

 

Small cell carcinoma. The tumor consists of sheets of small cells with a brisk mitotic rate, scant cytoplasm, finely granular nuclear chromatin, and inconspicuous or absent nucleoli (H&E stain, x400).

TC is defined as a neuroendocrine tumor with fewer than 2 mitoses per 2 mm2 and no necrosis (see Fig. 9-5). AC is defined as a neuroendocrine tumor that meets one of the two criteria: 2-10 mitoses per 2 mm2 or necrosis (see Fig. 9-6). In contrast to the high-grade neuroendocrine tumors, TC and AC do not occur in combination with other types of carcinoma. The number of mitoses and necrosis may be present only focally within a given tumor. Therefore, accurate classification of carcinoid tumors into TC or AC may not be possible in limited biopsy specimens with scant diagnostic material, and a definite diagnosis may require larger fragments of tumor. In these situations, it is recommended that small biopsies be signed as "carcinoid tumor" and the appropriate classification be performed on thorough examination of the resected specimens.12,13

LCNEC is defined as a neuroendocrine tumor with more than 10 mitoses per 2 mm2 and cytologic features of LCC (see Fig. 9-7). These features include cells with polygonal shape, abundant cytoplasm, and prominent nucleoli. Evidence of neuroendocrine differentiation must be demonstrated by performing immunohistochemistry for the specific neuroendocrine markers chromogranin and synaptophysin.Only tumors that show both neuroendocrine morphology and positive staining should be classified as LCNEC. It is important to note that up to 20% of conventional adenocarcinoma, small cell carcinoma (SCC) or LCC, will stain with neuroendocrine markers. Such tumors have been designated as non–small cell lung carcinoma with neuroendocrine differentiation.

SCLC is defined as a neuroendocrine tumor with more than 10 mitoses per 2 mm2 and small cell cytologic features (see Fig. 9-8). Cells have an oval or vaguely spindled shape and have scant cytoplasm. Nuclei are hyperchromatic and have absent or very small nucleoli (see Fig. 9-8). Crush artifact may be prominent on small biopsies, but this is not pathognomonic for the diagnosis of SCC. In larger-core biopsies or resected specimens, the cells may appear slightly larger than in a transbronchial biopsy and may have distinct cytoplasm. Numerous prominent nucleoli and large cells should not be seen.

LCNEC and SCLC may occur in combination with other NSCLCs as well as with each other. Such tumors are termed combined LCNEC, combined SCLC, and combined SCLC/LCNEC, respectively.19 While the two high-grade neuroendocrine tumors show numerous similarities, they are retained in separate classifications because LCNEC currently has not been shown to respond to chemotherapy in the same fashion as SCLC. Surgery is the currently preferred treatment for LCNEC, although further study of this relatively newly defined tumor is ongoing.20–23

Immunohistochemical Staining

Immunohistochemistry is used routinely in the pathology laboratory for the diagnosis of lung tumors. Immunostains are used (1) to differentiate primary pulmonary adenocarcinoma from metastatic adenocarcinoma to the lung, (2) to distinguish adenocarcinoma from malignant mesothelioma, and (3) to determine the neuroendocrine status of tumors.

DIFFERENTIATION BETWEEN PRIMARY PULMONARY ADENOCARCINOMA AND METASTATIC ADENOCARCINOMA

The morphologic features of primary adenocarcinoma of the lung may be similar to the features of an adenocarcinoma that is metastatic from a distant primary site. Although the presence of multiple nodules often leads to the presumptive diagnosis of metastases, multifocal adenocarcinoma is not rare and needs to be distinguished from metastases. Furthermore, patients with a solitary pulmonary nodule may have metastatic adenocarcinoma to the lung as the first presentation of disease.

TTF-1 is a homeodomain-containing transcription factor that regulates tissue-specific expression of surfactant apoprotein A, surfactant apoprotein B, surfactant apoprotein C, Clara cell antigen, and T1. TTF-1 is very important in distinguishing primary from metastatic adenocarcinoma because most of the cases of primary carcinomas are positive, whereas metastatic adenocarcinoma to lung is virtually always TTF-1-negative (Fig. 9-9A ). Lung cancer subtypes have different TTF-1 expression: 75% positive in adenocarcinoma, 85% positive in SCC, and rarely in the squamous cell and LCC.

Figure 9-9.

 
 

Adenocarcinoma from a patient with a solitary lung nodule. The pathologic features of metastatic and primary adenocarcinoma are often indistinguishable. Tumor cells (upper left corner) and normal alveolar epithelium (lower left corner) are positive for CK7 (A) and TTF-1 (B).

 

Pulmonary adenocarcinoma of the lung is usually CK7+ and CK20– and therefore distinguishable from CK7– and CK20+ metastatic adenocarcinoma of the colorectum. CDX-2 is a highly specific and sensitive marker for metastatic gastrointestinal malignancies that could be used to differentiate these gastric entities from primary lung tumors (Fig. 9-9B ).

Although squamous cell carcinoma (Fig. 9-10) is usually p63-positive, there is no marker to date that is able to distinguish between primary and metastatic squamous cell carcinoma. However, p63 is an important immunostain in cases of poorly differentiated NSCLC, where the distinction between adenocarcinoma and squamous cell carcinoma is virtually impossible to make on the basis of hematoxylin and eosin-stained slides alone (Fig. 9-11).

Figure 9-10.

 

Moderately differentiated squamous cell carcinoma (H&E stain, x200).

 

Figure 9-11.

 

In this case of squamous cell carcinoma, the tumor cells are positive for p63 (x200).

DETERMINING THE NEUROENDOCRINE STATUS OF TUMORS

Both chromogranin (reacts with cytoplasmic neuroendocrine granules) and synaptophysin (reacts with a cell membrane glycoprotein) are used to diagnose the neuroendocrine tumors of the lung. All typical and atypical carcinoid tumors stain with chromogranin and synaptophysin, whereas SCC is negative in 25% of cases (Figs. 9-12 and 9-13). Neuroendocrine markers are valuable in diagnosing NSCLC with neuroendocrine differentiation,a specific group of poorly differentiated tumors without a neuroendocrine morphology.

Figure 9-12.

 

Atypical carcinoid tumor positive for synaptophysin (x400).

 

Figure 9-13.

 

Large cell neuroendocrine carcinoma. Evidence of neuroendocrine differentiation must be demonstrated by performing immunohistochemistry for specific neuroendocrine markers. Tumor cells were positive for synaptophysin (x400).

DISTINGUISHING BETWEEN MALIGNANT MESOTHELIOMA AND LUNG ADENOCARCINOMA

Immunohistochemistry is most valuable in distinguishing between malignant mesothelioma and lung adenocarcinoma. A panel of four markers, two positive in mesothelioma and two negative in mesothelioma (but positive in adenocarcinoma), is used routinely in the pathology laboratory. The stains that are negative in mesothelioma but positive in adenocarcinoma include carcinoembryonic antigen, B72.3, Ber-EP4, and MOC31. The stains that are sensitive and specific for mesothelioma are WT-1, calretinin, D2-40, and cytokeratin 5/6 (Figs. 9-14, 9-15, and 9-16).

Figure 9-14.

 

Histopathology of diffuse malignant mesothelioma. Malignant tumor cells arranged in tubules and cords invade into the adipose tissue of the chest wall. Invasion into adipose and/or fibrous tissue of the chest wall is an important criterion for the diagnosis of diffuse malignant mesothelioma (H&E stain, x200).

 

Figure 9-15.

 

In diffuse malignant mesothelioma, the tumor cells are positive for calretinin (x200).

 

Figure 9-16.

 

Diffuse malignant mesothelioma cells positive for WT-1. Tumor cells have positive nuclear staining (x200).

SUMMARY

Surgical excision remains the only therapeutic modality that can cure selected lung cancer patients. Pathologists play an important role in the surgical management of patients with lung cancer from preoperative diagnosis and staging, to intraoperative evaluation of the extent of distant disease and margin status, to postoperative assessment of tumor genetic alterations. They offer guidance in selecting appropriate surgical therapies and chemotherapeutic regimens, as well as in identifying morphologic and molecular prognostic markers and predictors of response to therapeutic agents. They are expected to provide accurate diagnosis and classification of the patient's lung cancer. Most important, pathologists are required to provide pathologic staging information in lung resection specimens, surgical resection margin status, and information about lung cancer subtype.

Tumor stage, as determined by current American Joint Committee on Cancer guidelines, is considered to be one of the most important prognostic factors for patients with lung neoplasms. Frozen-section examination of mediastinal lymph nodes obtained by mediastinoscopy is used routinely to determine whether NSCLC patients will undergo tumor excision. Determination of the pT and pN status of the resected surgical pathology specimen determines whether the patient will be treated with postoperative chemotherapy and/or radiation therapy. Furthermore, classification algorithms based on the presence of genetic alterations found in lung cancer can be used to identify drugs or therapeutic agents targeting these alterations.

REFERENCES

1. Fossella FV, Komaki R, Putnam JB: Monograph on Lung Cancer. New York, Springer-Verlag, 2003.

2. Travis WD, Linnoila RI, Tsokos MG, et al: Neuroendocrine tumors of the lung with proposed criteria for large-cell neuroendocrine carcinoma: An ultrastructural, immunohistochemical, and flow cytometric study of 35 cases. Am J Surg Pathol 15:529–53, 1991. [PubMed: 1709558]

3. Faries MB, Bleicher RJ, Ye X, et al: Lymphatic mapping and sentinel lymphadenectomy for primary and metastatic pulmonary malignant neoplasms. Arch Surg 139:870–6; discussion 6–7, 2004. 

4. Rea F, Marulli G, Callegaro D, et al: Prognostic significance of main bronchial lymph nodes involvement in non-small cell lung carcinoma: N1 or N2Lung Cancer 45:215–20, 2004. [PubMed: 15246193]

5. Marchevsky AM: Problems in pathologic staging of lung cancer. Arch Pathol Lab Med 130:292–302, 2006. [PubMed: 16519556]

6. Okubo K, Kato T, Hara A, et al: Imprint cytology for detecting metastasis of lung cancer in mediastinal lymph nodes. Ann Thorac Surg 78:1190–3, 2004. [PubMed: 15464468]

7. Semik M, Netz B, Schmidt C, Scheld H: Surgical exploration of the mediastinum: mediastinoscopy and intraoperative staging. Lung Cancer 45:S55–61, 2004. 

8. Sihoe AD, Yim AP: Lung cancer staging. J Surg Res 117:92–106, 2004. [PubMed: 15013719]

9. Gephardt GN, Baker PB: Lung carcinoma surgical pathology report adequacy: A College of American Pathologists Q-Probes study of over 8300 cases from 464 institutions. Arch Pathol Lab Med 120:922–7, 1996. [PubMed: 12046605]

10. Travis WD, Sobin LH: Histological Typing of Lung and Pleural Tumours: International Histologic Classification of Tumours (No. 1). New York, Springer-Verlag, 1999.

11. Brambilla E, Travis WD, Colby TV, et al: The new World Health Organization classification of lung tumours. Eur Respir J 18:1059–68, 2001. [PubMed: 11829087]

12. Beasley MB, Brambilla E, Travis WD: The 2004 World Health Organization classification of lung tumors. Semin Roentgenol 40:90–7, 2005. [PubMed: 15898407]

13. Travis WD: World Health Organization, International Agency for Research on Cancer, International Academy of Pathology, and International Association for the Study of Lung Cancer. Pathology and Genetics of Tumours of the Lung, Pleura, Thymus and Heart. Lyon, IARC Press, 2004.

14. Jackman D, Chirieac L, Jänne P: Bronchioloalveolar carcinoma: A review of the epidemiology, pathology, and treatment. Semin Respir Crit Care Med 342–52, 2005. 

15. Travis WD, Garg K, Franklin WA, et al: Evolving concepts in the pathology and computed tomography imaging of lung adenocarcinoma and bronchioloalveolar carcinoma. J Clin Oncol 23:3279–87, 2005. [PubMed: 15886315]

16. Goldstein NS, Thomas M: Mucinous and nonmucinous bronchioloalveolar adenocarcinomas have distinct staining patterns with thyroid transcription factor and cytokeratin 20 antibodies. Am J Clin Pathol 116:319–25, 2001. [PubMed: 11554157]

17. Shah RN, Badve S, Papreddy K, et al: Expression of cytokeratin 20 in mucinous bronchioloalveolar carcinoma. Hum Pathol 33:915–20, 2002. [PubMed: 12378517]

18. Asamura H, Kameya T, Matsuno Y, et al: Neuroendocrine neoplasms of the lung: A prognostic spectrum. J Clin Oncol 24:70–6, 2006. [PubMed: 16382115]

19. Nicholson SA, Beasley MB, Brambilla E, et al: Small cell lung carcinoma (SCLC): A clinicopathologic study of 100 cases with surgical specimens. Am J Surg Pathol 26:1184–97, 2002. [PubMed: 12218575]

20. Iyoda A, Hiroshima K, Baba M, et al: Pulmonary large cell carcinomas with neuroendocrine features are high-grade neuroendocrine tumors. Ann Thorac Surg 73:1049–54, 2002. [PubMed: 11996239]

21. Takei H, Asamura H, Maeshima A, et al: Large cell neuroendocrine carcinoma of the lung: A clinicopathologic study of eighty-seven cases. J Thorac Cardiovasc Surg 124:285–92, 2002. [PubMed: 12167788]

22. Zacharias J, Nicholson AG, Ladas GP, Goldstraw P: Large cell neuroendocrine carcinoma and large cell carcinomas with neuroendocrine morphology of the lung: Prognosis after complete resection and systematic nodal dissection. Ann Thorac Surg 75:348–52, 2003. [PubMed: 12607637]

23. Rossi G, Cavazza A, Marchioni A, et al: Role of chemotherapy and the receptor tyrosine kinases KIT, PDGFR, PDGFR, and Met in large-cell neuroendocrine carcinoma of the lung. J Clin Oncol 23:8774–85, 2005. [PubMed: 16314638]



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