TY - JOUR
T1 - Simultaneous immunohistochemical expression of HBME-1 and galectin-3 differentiates papillary carcinomas from hyperfunctioning lesions of the thyroid
AU - Rossi, Esther
AU - Raffaelli, Marco
AU - Mule', Antonino
AU - Miraglia, Antonella
AU - Lombardi, Celestino Pio
AU - Vecchio, Fabio Maria
AU - Fadda, Guido
PY - 2006
Y1 - 2006
N2 - AIMS: The histological diagnosis is critical for the postsurgical management and
follow-up of thyroid malignancies. The differential diagnosis between papillary
carcinoma and hyperfunctioning lesions, either with papillary hyperplasia or with
a follicular architecture, can create real diagnostic difficulty. The aim of this
study was to evaluate the expression of several antibodies considered to be
markers of malignancy in malignant and hyperfunctioning thyroid neoplasms and to
include the most effective of them in a diagnostic panel.
METHODS AND RESULTS: One hundred resected thyroid nodules--58 hyperfunctioning
benign lesions and 42 papillary carcinomas (14 follicular variant, 14
macrofollicular variant and 14 classic type)--were immunohistochemically studied
for HBME-1, galectin-3, cytokeratin (CK) 19 and RET-proto-oncogene. HBME-1 and
galectin-3 showed 92.8% and 89% sensitivity, respectively, and their coexpression
was present in 36 out of 42 papillary carcinomas (85.7%) and absent in
non-malignant lesions. Their association increased sensitivity to 94.7% and the
diagnostic accuracy to 97.9% and involved the highest number of cases (95%) in
comparison with two other panels including, respectively, three (HBME-1,
galectin-3, CK19) and all four antibodies.
CONCLUSION: An immunohistochemical panel consisting of HBME-1 and galectin-3 can
make a correct distinction between malignant and hyperfunctioning thyroid
neoplasms with high diagnostic accuracy.
AB - AIMS: The histological diagnosis is critical for the postsurgical management and
follow-up of thyroid malignancies. The differential diagnosis between papillary
carcinoma and hyperfunctioning lesions, either with papillary hyperplasia or with
a follicular architecture, can create real diagnostic difficulty. The aim of this
study was to evaluate the expression of several antibodies considered to be
markers of malignancy in malignant and hyperfunctioning thyroid neoplasms and to
include the most effective of them in a diagnostic panel.
METHODS AND RESULTS: One hundred resected thyroid nodules--58 hyperfunctioning
benign lesions and 42 papillary carcinomas (14 follicular variant, 14
macrofollicular variant and 14 classic type)--were immunohistochemically studied
for HBME-1, galectin-3, cytokeratin (CK) 19 and RET-proto-oncogene. HBME-1 and
galectin-3 showed 92.8% and 89% sensitivity, respectively, and their coexpression
was present in 36 out of 42 papillary carcinomas (85.7%) and absent in
non-malignant lesions. Their association increased sensitivity to 94.7% and the
diagnostic accuracy to 97.9% and involved the highest number of cases (95%) in
comparison with two other panels including, respectively, three (HBME-1,
galectin-3, CK19) and all four antibodies.
CONCLUSION: An immunohistochemical panel consisting of HBME-1 and galectin-3 can
make a correct distinction between malignant and hyperfunctioning thyroid
neoplasms with high diagnostic accuracy.
KW - Carcinoma, Papillary
KW - Diagnosis, Differential
KW - Galectin 3
KW - Humans
KW - Hyperplasia
KW - Immunohistochemistry
KW - Keratins
KW - Proto-Oncogene Proteins c-ret
KW - Reproducibility of Results
KW - Sensitivity and Specificity
KW - Thyroid Gland
KW - Thyroid Neoplasms
KW - Tumor Markers, Biological
KW - Carcinoma, Papillary
KW - Diagnosis, Differential
KW - Galectin 3
KW - Humans
KW - Hyperplasia
KW - Immunohistochemistry
KW - Keratins
KW - Proto-Oncogene Proteins c-ret
KW - Reproducibility of Results
KW - Sensitivity and Specificity
KW - Thyroid Gland
KW - Thyroid Neoplasms
KW - Tumor Markers, Biological
UR - http://hdl.handle.net/10807/12775
U2 - 10.1111/j.1365-2559.2006.02428.x
DO - 10.1111/j.1365-2559.2006.02428.x
M3 - Article
SN - 0309-0167
VL - 48
SP - 795
EP - 800
JO - Histopathology
JF - Histopathology
ER -