TY - JOUR
T1 - ERG expression in multiple myeloma—A potential diagnostic pitfall
AU - Knief, Juliana
AU - Reddemann, Katharina
AU - Gliemroth, Jan
AU - Brede, Swantje
AU - Bartscht, Tobias
AU - Thorns, Christoph
N1 - Publisher Copyright:
© 2016 Elsevier GmbH
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Introduction ERG expression has been described as a frequent event in prostate cancer indicating poor prognosis and promoting oncogenesis. It has also been demonstrated in Ewing's sarcoma, acute myeloid leukemia and acute T-lymphoblastic leukemia but could not be found in other epithelial tumors, Hodgkin's or Non-Hodgkin's lymphoma. We aimed to analyze ERG expression in multiple myeloma, following an index case of a patient with metastases of unknown origin in the spine strongly expressing ERG, which were thought to be of prostatic origin but turned out to be plasmacytic lesions. Material and methods We subsequently selected 12 formalin-fixed, paraffin-embedded tissue samples of multiple myeloma from our archives and performed immunohistochemical staining for ERG. Results All 12 analyzed cases showed strong nuclear expression of ERG in >90% of tumor cells (myeloma cells). Conclusions This report highlights a potential and critical diagnostic pitfall in biopsy specimens where morphology is only of limited assistance in reaching the correct diagnosis. It urges pathologists to exercise caution in cases where strong ERG-positivity implicates the presence of a prostatic neoplasia and illustrates the need for further immunohistochemical examination.
AB - Introduction ERG expression has been described as a frequent event in prostate cancer indicating poor prognosis and promoting oncogenesis. It has also been demonstrated in Ewing's sarcoma, acute myeloid leukemia and acute T-lymphoblastic leukemia but could not be found in other epithelial tumors, Hodgkin's or Non-Hodgkin's lymphoma. We aimed to analyze ERG expression in multiple myeloma, following an index case of a patient with metastases of unknown origin in the spine strongly expressing ERG, which were thought to be of prostatic origin but turned out to be plasmacytic lesions. Material and methods We subsequently selected 12 formalin-fixed, paraffin-embedded tissue samples of multiple myeloma from our archives and performed immunohistochemical staining for ERG. Results All 12 analyzed cases showed strong nuclear expression of ERG in >90% of tumor cells (myeloma cells). Conclusions This report highlights a potential and critical diagnostic pitfall in biopsy specimens where morphology is only of limited assistance in reaching the correct diagnosis. It urges pathologists to exercise caution in cases where strong ERG-positivity implicates the presence of a prostatic neoplasia and illustrates the need for further immunohistochemical examination.
UR - http://www.scopus.com/inward/record.url?scp=85007338142&partnerID=8YFLogxK
U2 - 10.1016/j.prp.2016.10.014
DO - 10.1016/j.prp.2016.10.014
M3 - Journal articles
C2 - 27913051
AN - SCOPUS:85007338142
SN - 0344-0338
VL - 213
SP - 130
EP - 132
JO - Pathology Research and Practice
JF - Pathology Research and Practice
IS - 2
ER -