Cytomorphology of paediatric hepatocellular carcinoma: A useful diagnostic adjunct

Author:

Nalwa Aasma1,Nakra Tripti2ORCID,Yadav Rajni3ORCID,Walia Ritika3,Agarwala Sandeep4,Jana Manisha5,Jain Deepali3ORCID,Das Prasenjit3,Mathur Sandeep R.3,Iyer Venkateswaran K.3

Affiliation:

1. Department of Pathology All India Institute of Medical Sciences Jodhpur India

2. Department of Pathology, University College of Medical Sciences University of Delhi Delhi India

3. Department of Pathology All India Institute of Medical Sciences New Delhi India

4. Department of Paediatric Surgery All India Institute of Medical Sciences New Delhi India

5. Department of Radiodiagnosis All India Institute of Medical Sciences New Delhi India

Abstract

AbstractIntroductionHepatocellular carcinoma (HCC) is a common primary malignancy of the liver but is rare in the paediatric age group; thus, it may be misdiagnosed as the more common tumour, hepatoblastoma. Management varies in both these tumours, and pathological diagnosis thus plays an important role for definitive therapy. Only a few case reports available in the literature have described the cytological characteristics of paediatric HCC. The present study was thus planned to evaluate the cytomorphological features of paediatric HCC.MethodsCases diagnosed with HCC on ultrasound‐guided fine needle aspiration cytology over a period of 14 years were retrieved. The cases were evaluated for detailed cytological features including cellularity, architecture, sinusoidal wrapping, trabecular thickness, necrosis, anisonucleosis, chromatin, nucleoli, nuclear contours, bi‐ or multinucleation, intranuclear and intracytoplasmic inclusions, naked nuclei, extra‐medullary haematopoiesis, monomorphism, and nuclear overlapping.ResultsTwelve cases of HCC were included in the study. The median age at diagnosis was 10 years. Serum alpha‐fetoprotein level was raised in most of them. Five of the 12 cases were characterised as moderately differentiated, three as poorly differentiated, two as well differentiated, and two as the fibrolamellar type of HCC. Cytohistological correlation was performed in seven cases.ConclusionsUltrasound‐guided fine needle aspiration serves as a useful tool to diagnose paediatric HCC and differentiate it from other primary hepatic malignancies, especially hepatoblastoma which closely mimics HCC in this age group, as serum alpha protein levels and imaging findings are unable to distinguish these two tumours.

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

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