Extraintestinal Endosonography


Introduction

The use of endoscopic ultrasound (EUS) has grown over the last 30 years, and it is now a well-established diagnostic method for the assessment of a range of gastrointestinal (GI) disorders, including the evaluation and staging of many types of endoluminal cancers. This chapter discusses EUS applications relating to extraintestinal structures, organs, and lesions. The objectives of this chapter are to review the utility of EUS for evaluating the mediastinum in both benign and malignant disease processes, including the detection of mediastinal lymph node metastases in lung cancer. Mass lesions in the paragastric and retroperitoneal organs (excluding the bile duct, gallbladder, and pancreas) are reviewed, including detection of lesions of the adrenal gland, liver, and kidneys. Ascites and pleural fluid are examined along with unusual extraintestinal lesions.

Lung Cancer

Lung cancer is the leading cause of cancer death in the United States in men and women, and has an overall 5-year survival rate of 15%. Treatment decisions are based on the location and extent of the tumor. The presence of extrapulmonary metastasis is crucial because patients without mediastinal involvement are potential candidates for resection. The distinction between non–small-cell lung cancer (NSCLC), which accounts for 80% of tumors, and small-cell lung cancer (SCLC), which accounts for 20% of tumors, is important because of the more aggressive nature of SCLC. SCLC is usually classified as limited or extensive disease, although the criteria for these two categories remain controversial. Although the TNM (primary tumor, regional nodes, metastases) staging system traditionally has not been used in staging SCLC, studies have suggested using the 7th edition of the TNM classification scheme for clinical trials and registry information, to guide future management. The forthcoming 8th edition of the TNM classification system has proposed changes to the T classification scheme, highlighting tumor size as a key feature. Metastatic disease is detected in 80% of SCLC cases at the time of diagnosis and tends to spread quickly so that surgery is considered less often in SCLC compared with NSCLC. Although highly responsive to radiotherapy and chemotherapy, SCLC usually recurs within 2 years.

In comparison, half of NSCLC cases are localized or locally advanced and can be treated by surgery, the cornerstone of therapy for NSCLC, or with adjuvant therapy with or without resection. NSCLC, which includes adenocarcinoma, squamous cell cancer, and large-cell cancer, was previously staged using the 2002 International Staging System. Recently, NSCLC, has been staged using the 7th edition until December 31, 2017 ( Box 47.1 ) and subsequently will be staged using the future 8th edition. This section focuses on EUS applications in the diagnosis and staging of NSCLC, although much of what is covered can be applied to SCLC.

Box 47.1
Adapted from Goldstraw P, Crowley J, Chansky K, et al: The IASLC Lung Cancer Staging Project: proposals for the revision of the TNM stage groupings in the forthcoming (seventh) edition of the TNM classification of malignant tumours. J Thorac Oncol 2(8):706–714, 2007.
International Staging System for Lung Cancer, 2007

Primary Tumor (T)

  • Tx: Primary tumor cannot be assessed

  • T0: No evidence of primary tumor

  • Tis: Carcinoma in situ

  • T1: Tumor < 3 cm without bronchoscopic evidence of invasion more proximal than the lobar bronchus (not the main bronchus unless superficial tumor of any size with invasion limited to the bronchial wall, which may extend proximal to the main bronchus)

    • T1a: Tumor < 2 cm in size

    • T1b: Tumor > 2 cm but < 3 cm in size

  • T2: Tumor > 3 cm but <7 cm, or any size with any of the following:

    • Involves the main bronchus (at least 2 cm distal to the carina)

    • Invades visceral pleura

    • Associated with atelectasis or obstructive pneumonitis that extends to the hilar region but does not involve the entire lung:

  • T2a: Tumor > 3 cm but <5 cm

  • T2b: Tumor > 5 cm but <7 cm

  • T3: Tumor > 7 cm or directly invades any of the following:

    • Chest wall, diaphragm, mediastinal pleura, or parietal pericardium or tumor in the main bronchus < 2 cm distal to the carina (without involvement of the carina)

    • Atelectasis or obstructive pneumonitis of the entire lung

    • Separate tumor nodules in the same lobe

  • T4: Tumor of any size that invades any of the following:

    • Mediastinum, heart, great vessels, trachea, esophagus, vertebral body, or carina

    • Separate tumor nodules in a different ipsilateral lobe

Nodal Involvement (N)

  • Nx: Regional lymph nodes cannot be assessed

  • N0: No regional lymph nodes metastasis

  • N1: Metastasis to ipsilateral peribronchial or ipsilateral hilar lymph nodes, or both, and intrapulmonary nodes including involvement by direct extension of primary tumor

  • N2: Metastasis to ipsilateral mediastinal or subcarinal lymph nodes, or both

  • N3: Metastasis to contralateral mediastinal, contralateral hilar, ipsilateral or contralateral scalene, or supraclavicular lymph nodes

Metastasis (M)

  • Mx: Distant metastasis cannot be assessed

  • M0: No distant metastasis

  • M1: Distant metastasis present

  • M1a: Separate tumor nodules in a contralateral lobe; tumor with pleural nodules or malignancy pleural or pericardial effusion

  • M1b: Distant metastasis

Stage Grouping

  • Occult carcinoma: TxN0M0

  • Stage 0: TisN0M0

  • Stage IA: T1a-bN0M0

  • Stage IB: T2aN0M0

  • Stage IIA: T1N1M0, T2bN0M0

  • Stage IIB: T2bN1M0, T3N0M0

  • Stage IIIA: T1N2M0, T2N2M0, T3N1-2M0, T4N0-1M0

  • Stage IIIB: T4 N2M0, Any TN3M0

  • Stage IV: Any T any N M1-b

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