96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...
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Abstracts<br />
study was to evaluate the expression and mutational status of potential<br />
molecular therapeutic targets in synovial sarcomas.<br />
Methods. 38 well characterized and molecularly confirmed cases of synovial<br />
sarcomas were included in this study. Immunohistochemical stainings<br />
of tyrosine kinase receptors of the EGF-R family (EGF-R, HER2/<br />
neu, HER3, HER4), the hepatocyte growth factor c-met, and signaling<br />
molecules implicated in the mTOR pathway (AKT, mTOR, PTEN), as<br />
well as E-Cadherin and snail was performed. In addition, cases were<br />
screened for mutations in the EGFR, PIK3C, B-RAF, K-RAS and N-RAS<br />
genes.<br />
Results. Members oft the EGF-receptor family of kinases as well as E-<br />
Cadherin and snail are important for defining the tumor phenotype by<br />
determining epithelial-mesenchymal transition of synovial sarcomas.<br />
Activation of c-met and signaling molecules oft the mTOR pathway are<br />
seen in a significant number of cases. Mutations of the genes studied<br />
(EGFR, PIK3C, B-RAF, K-RAS, N-RAS) are an overall rare event in synovial<br />
sarcomas.<br />
Conclusions. EGF-R expression is found in many synovial sarcomas, however,<br />
activating mutations in the tyrosine kinase domain or downstream<br />
signaling molecules appear to be a rare event or are absent. Activation<br />
of c-met and molecules oft the mTOR pathway is frequently seen in<br />
synovial sarcomas. The benefit of targeted therapy against these genes in<br />
synovial sarcomas remains to be determined.<br />
DO-084<br />
Allergy to metal implants: Immunological und histological analysis<br />
of patients with intolerance reaction after knee arthroplasty<br />
J . Schnei<strong>der</strong>1 , M . Flaig1 , B . Summer1 , C . von <strong>der</strong> Helm1 , C . Schopf1 , V . Krenn2 ,<br />
M . Thomsen3 , L . Frommelt4 , P . Thomas1 1 2 Ludwig-Maximilians-University, Munich, Dermatology, München, Zentrum<br />
<strong>für</strong> Histologie, Zytologie und Molekulare Diagnostik Trier, 3Orthopädische- DRK-Klinik, Baden-Baden, 4Endoklinik, Hamburg<br />
Aims. Allergic reaction to metal implants as a reason for implant loosening<br />
or other complications is controversially discussed. Therefore we<br />
analysed 10 patients with metal allergy but no infection or mechanical<br />
problems in knee arthroplasty who needed revision surgery.<br />
Methods. In periprosthetic tissue of the 10 patients with metal hypersensitivity<br />
(patch testing and/or lymphocyte transformation test (LTT)<br />
positive) and CoCrMo based arthroplasty, histological classification (according<br />
to consensus classification of periprosthetic interface membranes)<br />
and molecular cytokine analysis (Realtime-PCR) was performed.<br />
The results were compared with a control group of 5 patients without<br />
metal hypersensitivity. After implant replacement to titanium or oxinium<br />
based arthroplasty the symptoms were monitored with the WO-<br />
MAC-Score.<br />
Results. Patch testing: 4/10 reactivity to nickel, 3/10 to cobalt, 1/10 to chromium.<br />
Enhanced LTT reactivity: 8/10 to nickel, 1/10 to cobalt. Cytokine<br />
expression: IFNy 4/10 vs. 0/5; TGFβ 8/10 vs. 5/5; IL-8 8/10 vs. 0/5; IL-6 6/10<br />
vs. 1/5, IL10 7/10 vs. 5/5. In histopathology primarily the indeterminate<br />
type of periprosthetic tissue (type IV) or arthrofibrosis and a varying<br />
degree of lymphocytic infiltration were detected. The WOMAC-Score<br />
increased from 40.4±20.58 to 55.59±20.14.<br />
Conclusions. The combination of allergological, immunological and histopathological<br />
diagnostic steps helps to identify patients with implant<br />
intolerance reaction and may support the decision to a replacement with<br />
alternative material, such as titanium based arthroplasty.<br />
34 | Der Pathologe · Supplement 1 · 2012<br />
DO-085<br />
Expression patterns of microRNA in SFT – prediction of malignancy?<br />
C . Poremba1 , C . Altmann1 , N . Arens1 , J . Kriegsmann1 , P . Knöß2 1Research Park Trier, Center of Histopathology, Cytology and Molecular<br />
Diagnostics (CHCMD) Trier, Trier, 2Center of Histopathology, Cytology and<br />
Molecular Diagnostics Trier<br />
Aims. The clinical and biologic behavior of solitary fibrous tumor (SFT)<br />
has been a problematic issue, mainly because of inconclusional criteria.<br />
SFT harboring “malignant” features such as high cellularity, >4 mitotic<br />
figures/10HPF and necrosis/hemorrhage are at risk for metastasis/recurrence.<br />
However, in biopsies those criteria may not be evident. In our<br />
study, we analyze if expression patterns of microRNA, a class of posttranscriptional<br />
regulators, differs between localized, relapsed and metastatic<br />
SFT, and may help to predict clinical and biologic behavior in this<br />
tumor entity.<br />
Methods. In this pilot study, tumor tissues from 6 patients suffering from<br />
SFT (3 localized without recurrence/metastasis, 3 with recurrence/metastasis)<br />
are analyzed by microRNA assay (Applied Biosystems, Carlsbad,<br />
CA USA). Clinical follow-up is available up to 10 years after initial diagnosis.<br />
Expression patterns of microRNAs are compared between localized<br />
SFT versus relapsed/metastatic SFT and within this group between<br />
the initial tumor (areas of different cellularity) and its respective recurrence/metastasis<br />
after microdissection.<br />
Results. In ongoing analyses, expression patterns of microRNAs are<br />
compared between localized vs. relapsed/metastatic SFT and are correlated<br />
to clinical outcome.<br />
Conclusions. We investigate if different expression patterns of microR-<br />
NAs between localized vs. metastatic/relapsed SFT may help to identify<br />
patients with higher risk for unfavourable clinical outcome based on the<br />
initial biopsy of SFT. Statistical analyses are ongoing.<br />
DO-086<br />
Defining arthrofibrosis in histopathological specimens:<br />
an evolving concept<br />
P . Knöß1 , C . Dierkes1 , M . Ruppert2 , T . Gehrke3 , D . Kendoff3 , C . Theiß4 , V . Krenn1 1Medical health center for histology, cytology and molecular diagnostics<br />
Trier, 2Brothers of mercy hospital Trier, 3ENDO Clinic Hamburg, 4Ruhr University<br />
Bochum<br />
Aims. Arthrofibrosis is the most severe complication in endoprothetic<br />
surgery leading to a complete loss of joint function. In the past we reported<br />
a proposal for a histopathological grading system for arthrofibrosis<br />
(grade 1–3). This time we wanted to verify our results immunohistochemically<br />
using β-catenin, a marker known for his association with fibromatosis.<br />
Methods. 262 specimens of patients with clinical evidence of arthrofibrosis<br />
were graded semiquantitatively for fibroblast density using our<br />
proposed grading system, stained with antibodies against β-Catenin and<br />
compared with a reference group of 29 neosynovialitis type 4 specimens.<br />
Results. In 85.1% of the specimens the histopathologic diagnosis was arthrofibrosis.<br />
The distribution for the fibroblast density was 28.8% grade 1,<br />
47.7% grade 2 and 23.4% grade 3. The cellularity was significantly higher<br />
in every arthrofibrosis grade than in the reference group (p