Abstract
The role of fine needle aspiration biopsy (FNAB) in the evaluation of focal liver lesions has evolved. Guided FNAB is still useful to procure a tissue diagnosis if clinical, biochemical and radiologic findings are inconclusive. Major diagnostic issues include: (i) Distinction of benign hepatocellular nodular lesions from reactive hepatocytes, (ii) Distinction of well-differentiated hepatocellular carcinoma (WD-HCC) from benign hepatocellular nodular lesions, (iii) Distinction of poorly differentiated HCC from cholangiocarcinoma and metastatic carcinomas, (iv) Determination of histogenesis of malignant tumor, and (v) Determination of primary site of origin of malignant tumor. This review gives a general overview of hepatic FNAB; outlines an algorithmic approach to cytodiagnosis with emphasis on HCC, its variants and their mimics; and addresses current diagnostic issues. Close radiologic surveillance of high-risk cirrhotic patients has resulted in the increasing detection of smaller lesions with many subjected to biopsy for tissue characterization. The need for tissue confirmation in clinically obvious HCC is questioned due to risk of malignant seeding. When a biopsy is indicated, core needle biopsy is favored over FNAB. The inherent difficulty of distinguishing small/early HCC from benign hepatocellular nodular lesions has resulted in indeterminate reports. Changing concepts in the understanding of the biological behavior and morphologic evolution of HCC and its precursors; and the current lack of agreement on the morphologic criteria for distinguishing high-grade dysplastic lesions (with small cell change) from WD-HCC, have profound impact on nomenclature, cytohistologic interpretation and management. Optimization of hepatic FNAB to enhance the yield and accuracy of diagnoses requires close clinicopathologic correlation; combined cytohistologic approach; judicious use of ancillary tests; and skilled healthcare teams.
Highlights
CytoJournal 2005, 2:7 http://www.cytojournal.com/content/2/1/7 from an ever-expanding array of tumor markers and sophisticated imaging modalities
Critical refinement of current histopathologic criteria for the diagnosis of small ("early") hepatocellular carcinoma (HCC) is necessary with increasing demands for tissue characterization of small "suspicious" nodules [13,14,15,16,17]
The review gives an algorithmic approach to the fine needle aspiration biopsy (FNAB) diagnosis of focal liver lesions; an overview of current diagnostic issues concerning hepatic FNAB; problems and pitfalls in the cytodiagnosis of well-differentiated hepatocellular nodular lesions; and diagnostic utility of immunohistochemistry
Summary
Tissue confirmation is recommended in the diagnosis of focal liver lesions as the risk of aggressive therapy is greater than the risk of malignant seeding. The lack of tissue can be overcome by using cutting aspiration needles that can provide material for smear cytology and microhistology. Optimization of FNAB in the diagnosis of focal liver lesions, increase in the yield of true positive diagnoses, and rendering of fewer indeterminate reports require close clinicopathologic correlation; combination of smear cytology and microhistology, use of a discriminant panel of special and immunostains; and team work by skilled operators on all fronts. HCC : Hepatocellular carcinoma MRN : Macroregenerative nodule DN : Dysplastic nodule FNH : Focal nodular hyperplasia LCA : Liver cell adenoma WD-HCC : Well-differentiated hepatocellular carcinoma PD-HCC : Poorly differentiated hepatocellular carcinoma CC : Cholangiocarcinoma AFP : Alpha-fetoprotein CEA : Carcinoembyronic antigen N/C ratio : nuclear-cytoplasmic ratio CHCC-CC : Combined hepatocellular-cholangiocarcinoma pCEA : polyclonal carcinoembyronic antigen NET : Neuroendocrine tumor SCUC : Small cell undifferentiated carcinoma GIT : Gastrointestinal tract LCUC : Large cell undifferentiated carcinoma LS : Leiomyosarcoma GIST : Gastrointestinal stromal tumor CT : Computed tomography MRI : Magnetic resonance imaging US : Ultrasonography CNB : Core needle biopsy PCNA : Proliferating cell nuclear antigen
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