Skip to main content Accessibility help
×
Hostname: page-component-848d4c4894-2pzkn Total loading time: 0 Render date: 2024-06-07T13:12:23.432Z Has data issue: false hasContentIssue false

9 - Focal liver lesions in infants and children

Published online by Cambridge University Press:  05 April 2015

Aileen Wee
Affiliation:
National University of Singapore
Pichet Sampatanukul
Affiliation:
Chulalongkorn University, Thailand
Nirag Jhala
Affiliation:
University of Pennsylvania
Get access

Summary

INTRODUCTION

Lest it be overlooked, not all focal liver lesions detected in childhood are tumors. Infective/inflammatory lesions and cysts have to be considered too. Most pediatric malignancies are of the hematolymphoid type and do not usually form mass lesions. Primary malignant tumors of the liver are uncommon and represent about 1.3% of all malignancies in childhood. Hepatoblastoma (HB) and hepatocellular carcinoma (HCC) are the most common primary malignant tumors of the liver and represent about two-thirds of all hepatic neoplasms. Metastases from malignancies elsewhere, for example the group of small round blue cell tumors (SRBCT), are common differential diagnoses. Tumors of the liver are infrequently aspirated in the young. In most practices, the tumors are resected rather than subjected to preoperative fine needle aspiration biopsy (FNAB) or core biopsy.

CLINICAL PERSPECTIVE

Age at presentation helps one to prioritize the list of differential diagnoses when evaluating pediatric liver masses (Table 9.1). Abdominal distension, pain, hepatomegaly, and jaundice form the major manifestations. However, certain clinical settings tend to favor one diagnosis over another – for example, intermittent jaundice with radiologic demonstration of a tumor in relation to the biliary tree in a young patient (generally <2 years) is highly indicative of embryonal rhabdomyosarcoma.

PATHOLOGIC PERSPECTIVE

Recognition of and diagnostic approach to focal liver lesions is based on pattern recognition and predominant cell profiling (Chapter 2). In keeping with this approach, a diagnostic algorithm pertaining to the characterization of focal liver lesions in the young is presented. It is based on whether the tumors are of hepatocellular, biliary, or mesenchymal derivation with specific cell profiles (e.g., cells with epithelioid features, small round blue cells, large pleomorphic cells, and spindle or giant cells) (Table 9.2).

COMMON HEPATIC TUMORS

The following descriptions will focus on common specificentities in pediatric liver tumors. This chapter will not highlight features associated with tumors, such as HCC, focal nodular hyperplasia or lesions which have been covered in prior chapters. Table 9.3 highlights some of the distinguishing cytohistologic features of selected small round cell tumors that may affect the pediatric liver.

Hepatoblastoma

This is a primary malignant blastematous tumor of the liver characterized by various combinations of several epithelial and mesenchymal cell lineages.

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
×