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 />
SA-P-027<br />
Primary serous peritoneal carcinoma (PPC) with and without<br />
serous tubal in-situ carcinoma (STIC)<br />
L .-C . Horn 1 , K . Leonhardt 2 , K . Kellner 1 , R . Scherling 2 , J . Einenkel 2<br />
1 University of Leipzig, Institute of Pathology, Leipzig, 2 University of Leipzig,<br />
Department of Obstetrics and Gynecology (Institute of Trier), Leipzig<br />
Aims. Evaluating the frequency of serous tubal in situ carcinoma (STIC)<br />
in cases of primary peritoneal carcinoma.<br />
Methods. The present study evaluates immunohistochemically (Ki-67<br />
and p53-staining) the presence of STIC in completely embedded Fallopian<br />
tubes of 35 consecutive cases meeting the clinicopathologic criteria of<br />
primary high-grade serous carcinoma.<br />
Results. p53 signature was seen in four cases (11%) and STIC in seven patients<br />
(20%). All STIC occurred at the fimbriated end of the Fallopian tube<br />
and in one case a bilateral involvement was seen. These precursor lesions<br />
were missed during the initial routine screening. In two cases repeated<br />
staining for p53 was negative.<br />
Conclusions. STIC and p53-signature as precursor lesions of pelvic serous<br />
cancer are seen in some but not all cases of primary serous peritoneal<br />
cancer. Further studies are required to identify the source of serous cancer<br />
in cases without STIC-lesions.<br />
SA-P-028<br />
KPNA2 protein expression is an independent adverse predictor of<br />
survival in patients with endometrial carcinomas<br />
K . Ikenberg1 , A . Noske1 , R . Caduff1 , A . Dellas2 , H . Moch1 , P .J . Wild1 1University Hospital Zurich, Institute of Surgical Pathology, Zürich, Switzerland,<br />
2University of Basel, Institute of Pathology, Basel, Switzerland<br />
Aims. To analyze rates of expression of karyopherin alpha 2 (KPNA2),<br />
an important mediator of nucleocytoplasmic transport, in different endometrial<br />
cancer subtypes, and to evaluate its prognostic properties for<br />
patients with primary endometrial cancer.<br />
Methods. Tissue microarrays (TMA) contained 527 formalin-fixed, paraffin-embedded<br />
endometrial cancer tissue cores from two different<br />
institutes of pathology. TMAs were stained immunohistochemically for<br />
KPNA2 and p53.<br />
Results. KPNA2 expression was significantly upregulated in carcinomas<br />
of the endometrium and was significantly associated with higher tumor<br />
grade, higher FIGO stage, and overexpression of p53. KPNA2 expression<br />
was not associated with different subtypes of endometrial carcinomas.<br />
Positive nuclear KPNA2 immunoreactivity in at least 10% of nuclei was<br />
identified as a novel predictor of survival, and was independent of the<br />
well-established prognostic factors age, grade, FIGO stage, histological<br />
type, and p53 immunoreactivity in Cox regression analyses (hazard ratio=1.7,<br />
95% CI 1.13–2.56, p=0.01).<br />
Conclusions. KPNA2 is a novel independent prognostic marker for survival<br />
after hysterectomy. This may allow identifying patients who need<br />
more aggressive treatment.<br />
SA-P-029<br />
Loss of ARID1A/BAF250a expression in endometriosis – a new<br />
molecular mechanism for transformation into cancer?<br />
A . Noske1 , N . Samartzis2 , M . Rechsteiner1 , H . Moch1 , P . Imesch2 1University Hospital Zurich, Institute of Pathology, Zürich, Switzerland,<br />
2University Hospital Zurich, Dept . of Gynecology, Zürich, Switzerland<br />
Aims. Mutations of the tumor suppressor gene ARID1A are frequently<br />
found in endometriosis-associated ovarian carcinomas, and correlate<br />
with expression loss of the coding protein BAF250a. We hypothesize that<br />
deficient ARID1A/BAF250a expression may contribute in transformation<br />
of endometriosis into cancer.<br />
148 | Der Pathologe · Supplement 1 · 2012<br />
Methods. We evaluated ARID1A/BAF250a protein expression in 74 endometriosis,<br />
and 30 eutopic endometrium samples by immunohistochemistry.<br />
Further, an analysis of ARID1A/BAF250a and p53 expression in<br />
a cohort of 129 primary ovarian carcinomas was performed. To classify<br />
the ovarian carcinomas in type I and type II, the mutational status of p53,<br />
KRAS, and BRAF will be determined by deep-sequencing technology.<br />
Results. There was a loss of ARID1A/BAF250a expression in three endometriomas<br />
and one deep-infiltrating endometriosis, but in none of<br />
the peritoneal endometriosis and eutopic endometrium samples. Lack<br />
of expression was found in 22.5% of the ovarian carcinomas and was<br />
significantly associated with the endometrioid histological subtype and<br />
wild-type p53 protein.<br />
Conclusions. The deficiency of ARID1A/BAF250a expression in few endometriosis<br />
lesions may indicate an early event in malignant transformation<br />
of endometriosis. In context with the literature, the data support<br />
an association of ARID1A and p53 in ovarian cancer.<br />
SA-P-030<br />
Detection of micrometastasis in paraaortic lymph nodes in patients<br />
with carcinoma of the uterine cervix after negative frozen<br />
section analysis<br />
L .-C . Horn1 , K . Kellner1 , R . Scherling2 , M . Höckel2 , J . Einenkel2 1 2 University of Leipzig, Institute of Pathology, Leipzig, University of Leipzig,<br />
Department of Obstetrics and Gynecology (Institute of Trier), Leipzig<br />
Aims. Previous studies consi<strong>der</strong>ed the presence of micrometastases<br />
(MM) in pelvic lymph nodes as clinically relevant prognostic indicator<br />
and reported a 2.4 to 3.2 greater risk for recurrent disease and dead of<br />
the disease when compared to nodal negative patients. There is limited<br />
information about the value of (immunohistochemical) ultrastaging in<br />
negative para-aortic lymph nodes (PAN).<br />
Methods. Frozen section analysis was performed in all cases with PA-<br />
LNE because of clinical requirements. From all FS-blocks, routinely<br />
three step sections were performed. After FS-examination nodes were<br />
examined by one H&E-stained slide. All nodes without metastatic disease<br />
after frozen section and permanent section examination were subject<br />
of the present study. 43 patients and 418 PAN were enrolled and immunohistochemical<br />
staining using two cytokeratin-cocktail antibodies (AE<br />
1/AE 3 and KL-1) was performed. MM were defined as foci of tumor cells<br />
ranging from 0.2 mm to no more than 2 mm in size; isolated tumor cells<br />
(ITC) are defined as single tumor cells or small clusters of cells less than<br />
0.2 mm in size within the subcapsular sinuses of the lymph node.<br />
Results. In one case, one single node showed micrometastasis, representing<br />
an incidence of 2.3% of the studied cases and 0.23% of the examined<br />
lymph nodes. In three cases benign endosalpingiosis was seen. The<br />
patient with MM is alive without evidence of disease 96 months after<br />
surgery. ITC were not observed.<br />
Conclusions. The frequency of MM in PAN is very low. There are only limited<br />
data regarding their prognostic impact within the literature. After<br />
careful examination of all removed PAN using H&E-staining (and step<br />
sectioning), immunohistochemical ultrastaging cannot be recommend<br />
for routine use.<br />
SA-P-031<br />
Mismatch repair protein expression of cervical adenocarcinoma<br />
B . Helmchen1 , R . Brand2 , M . Kurrer3 , P . Komminoth1 , H .-P . Sinn2 1Community Hospital Triemli, Dept . of Pathology, Zürich, Switzerland,<br />
2University of Heidelberg, Institute for Pathology, Heidelberg,<br />
3Enge Institute of Pathology, Zürich, Switzerland<br />
Aims. Charakterisierung des immunhistochemischen Expressionsprofils<br />
<strong>der</strong> Mismatch-Repair-Proteine (MMRP) MLH1, MSH2, MSH6 und<br />
PMS2 an primären zervikalen Adenokarzinomen (ZAK) in Abgrenzung<br />
zu Karzinomen des unteren Uterinsegmentes (UUSK).