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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

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