Skip to main content Accessibility help
×
Hostname: page-component-78c5997874-4rdpn Total loading time: 0 Render date: 2024-11-14T16:31:57.763Z Has data issue: false hasContentIssue false

5 - Benign lung tumors and tumor-like lesions

Published online by Cambridge University Press:  05 January 2013

Syed Z. Ali
Affiliation:
The Johns Hopkins University School of Medicine
Grace C. H. Yang
Affiliation:
Cornell University, New York
Get access

Summary

Introduction

Of all the organs, lung is the most likely to have a false-positive cytologic diagnosis, because irritated type 2 pneumocytes can become markedly atypical with enlarged hyperchromatic nuclei and prominent nucleoli, mimicking adenocarcinoma. This chapter deals with benign lung tumors and non-infectious tumor-like lesions. In most hospitals, approximately 30% of the transthoracic fine needle aspiration (FNA) biopsies are benign. Some benign lesions, i.e., sarcoidosis, radiologically mimic malignancy, presenting as lung masses with hilar adenopathy. Positive positron emission tomography (PET scan) in a metastatic work-up can be alarming clinically. One needs to remember that a PET scan measures metabolic activity. Increased uptake can occur in metabolically active but benign lesions. Cytopathologists are sometimes under pressure from clinicians to overcall a lesion so the diagnosis matches clinical impression. One needs to remember that the truth lies in the cells and substances that are sampled from the lesion. Although bronchial brushes and transbronchial FNA are done by pulmonologists, the vast majority of the diagnostic cases in this author’s experience were obtained by radiologists using a percutaneous transthoracic approach.

PULMONARY HAMARTOMA

Clinical features

Pulmonary hamartomas account for about 75% of benign lung tumors. Grossly, the tumor is a sharply delineated and lobulated ovoid nodule, measuring up to 4 cm. It most commonly occurs in adults, usually men. It sometimes presents as an intrabronchial polypoid mass causing obstruction.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×