Background: Differentiation of hepatocellular carcinoma (HCC) from metastatic carcinoma in liver may be difficult on fine needle aspiration cytology (FNAC), especially when both appear as moderate to poorly differentiated tumours. A panel of immunocytochemical stains is frequently used in case of diagnostic difficulty. Recently, CD10 immunostain with a canalicular staining pattern has been shown to be a specific marker for hepatocytic differentiation. Objective: The present study was designed to assess the value of CD10 immunostain in distinguishing HCC from metastatic carcinoma in material obtained by FNAC of liver masses. Materials and methods: Formalin-fixed, paraffin-embedded cell blocks of 22 cases (7 cases of HCC and 15 cases of metastatic carcinoma), direct acetone-fixed smears and destained smears of 28 cases (18 cases of HCC and 10 cases of metastatic carcinoma) prepared from FNAC of the liver were immunostained using monoclonal antibody against CD10. Results: Seventeen (68%) of twenty-five cases of HCC were positive for CD10 with a canalicular staining pattern. Among them 7 (70%) of 10 cases were well-differentiated HCC and 10 (66%) of 15 cases were moderate to poorly differentiated HCC. Of 25 cases of metastatic carcinoma, four (16%) were positive for CD10 with a cytoplasmic (three cases) and membranous staining (one case) pattern. Conclusion: CD10 immunostaining is useful in discriminating HCC and metastatic carcinoma of the liver and is easily applied on cell blocks as well as FNAC smears.
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Li, HM
Wu, S
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Wu, S
Liew, CT
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Liew, CT
Loew, CK
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Loew, CK
Lau, JWY
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Lau, JWY
Lim, BK
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Lim, BK
Wang, XQ
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Wang, XQ
Chan, JYH
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG
Chan, JYH
Lee, JCK
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CHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONGCHINESE UNIV HONG KONG,PRINCE WALES HOSP,DEPT ANAT & CELLULAR PATHOL SURG CLIN ONCOL,SHATIN,HONG KONG