Korean J Pathol.
1999 Sep;33(9):717-722.
Immunohistochemical Findings in 10 Cases of Inflammatory Myofibroblastic Tumor
- Affiliations
-
- 1Department of Pathology, Pusan Paik Hospital, College of Medicine, Inje University, Pusan 614-735, Korea.
- 2Pusan National University Hospitall.
- 3Dong-A University Hospital.
Abstract
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A wide range of denomination has been used for inflammatory myofibroblastic
tumor (IMT). IMT is not entirely homogeneous, even though it shows some overlapping
histologic features such as haphazard proliferation of spindle cell and polymorphic
chronic inflammatory cell infiltraion. The spindle cell is considered to be of
myofibroblastic origin but follicular dendritic cell origin was reported recently. IMT is
known as nonneoplastic, aberrant inflammatory response. However, IMT could show
local invasion, recurrence, vascular invasion, and malignant transformation, and clonal
characteristics and aneuploidy of IMT support the hypothesis that IMT may be a
neoplastic process. In order to define the nature of spindle cell of IMT,
immunohistochemical stains for smooth muscle actin (SMA), vimentin (VMT), lysozyme,
S-100 protein, cytokeratin, CD21 were done. Additional immunohistochemical stains for
MIB-1 for proliferating activity and LMP (latent membrane protein) for Epstein-Barr
virus (EBV) were done. IMTs were composed of each 2 cases from lung, liver and
lymph node and one case from common bile duct, maxillary sinus, bladder and thigh,
and were histologically subclassified according to Coffin et al. Nine cases (90%) were
positive for SMA and VMT, but no correlation between SMA and VMT
immunoreactivity and histologic types was identified. Five cases (50%) were positive for
lysozyme and S-100 protein, and histologic type III was negative for lysozyme and
S-100 protein, and immunoreactivity for S-100 protein was different according to the
histologic subtypes. All 11 cases were negative for CD21 and EBV LMP. MIB-1
labelling index was less than 1% in all cases. In summary, the spindle cell is regarded
as myofibroblastic origin rather than follicular dendritic cell origin. Relationship with
EBV is not clear, and negligible MIB-1 reaction suggests that IMT might have a good
prognosis.