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96. Jahrestagung der Deutschen Gesellschaft für Pathologie e. V ...

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Abstracts<br />

DO-097<br />

Cytokeratin-positive epithelioid angiosarcoma presenting in the<br />

tonsil: a diagnostic challenge<br />

A . Agaimy 1 , H . Kirsche 2 , S . Semrau 3 , H . Iro 2 , A . Hartmann 1<br />

1 Friedrich-Alexan<strong>der</strong> University of Erlangen, Institute of Pathology, Erlangen,<br />

2 Friedrich-Alexan<strong>der</strong> University of Erlangen, Department of Otorhinolaryngology,<br />

Head and Neck Surgery, Erlangen, 3 Friedrich-Alexan<strong>der</strong> University of<br />

Erlangen, Department of Radiation oncology, Erlangen<br />

Aims. The majority of malignant neoplasms of the head and neck represent<br />

squamous cell carcinomas while sarcomas are rare in this anatomic<br />

region. Primary oral cavity sarcomas are exceedingly rare and may pose<br />

a great diagnostic challenge.<br />

Methods. A 71-year-old woman without previous history of malignancy<br />

or radiation to the head and neck presented with an antibiotic-refractory<br />

diffuse painful swelling of the right tonsil necessitating tonsillectomy.<br />

Within months the patient un<strong>der</strong>went surgical resection of multiple<br />

bleeding intraoral and gastrointestinal metastases. She is currently alive<br />

with disease 9 months from diagnosis.<br />

Results. Histological evaluation revealed subtotal replacement of the<br />

right tonsil by a high-grade epithelioid neoplasm displaying extensive<br />

ulceration, necrosis and primitive vasoformation. Immunohistochemistry<br />

showed strong/diffuse expression of pancytokeratin (CK) antibodies<br />

KL-1 and Lu5, CK8, CK18, CK19, vimentin, CD31, ERG and FLI-1. High<br />

molecular weight cytokeratins (CK5, 34ß12), CK7, CK13 and CK20 were<br />

not expressed.<br />

Conclusions. To our knowledge, this case represents the first well documented<br />

primary epithelioid angiosarcoma of the tonsil. The strong cytokeratin<br />

expression in epithelioid angiosarcomas represents a diagnostic<br />

pitfall. Thus, awareness of this rare and highly aggressive neoplasm is necessary<br />

for distinguishing it from poorly differentiated and acantholytic<br />

squamous cell carcinoma and diffuse large cell lymphoma.<br />

DO-098<br />

Lipomatous neoplasms of the salivary glands. A series of 23 cases<br />

with emphasis on oncocytic lipoadenoma and sebaceous differentiation<br />

A . Agaimy1 , B . Märkl2 , H . Arnholdt2 , J . Zenk3 , V . Bonkowsky4 , M . Michal5 ,<br />

A . Skalova5 , A . Hartmann1 , S . Ihrler6 1Friedrich-Alexan<strong>der</strong> University of Erlangen, Institute of Pathology, Erlangen,<br />

2Augsburg Clinic Center, Augsburg, 3Friedrich-Alexan<strong>der</strong> University of<br />

Erlangen, Department of Otorhinolaryngology, Head and Neck Surgery, Erlangen,<br />

4Nürnberg Clinic Center, Department of Otorhinolaryngology, Head<br />

and Neck Surgery, Nürnberg, 5Charles University, Medical Faculty Hospital,<br />

Department of Pathology, Pilsen, Czech Republic, 6Ludwig Maximilian University,<br />

Munich, Department of Pathology, München<br />

Aims. Lipomatous tumors of salivary glands are rare and have been the<br />

subject of rare case reports in the literature. Accordingly, their morphologic<br />

spectrum and clinicopathological features from a consecutive case<br />

series have not been studied.<br />

Methods. We collected 23 fatty tumors from consecutive surgical pathology<br />

files at four large hospitals (n=17) and from consultation files of two<br />

centers (n=6). Fat-containing pleomorphic adenoma and lipomatous<br />

myoepitheliomas were excluded.<br />

Results. There were 15 males and 8 females aged 18–89 yrs (mean, 55 yrs).<br />

Most tumors (n=21) originated in the parotid gland. Two affected the<br />

submandibular gland. Histologically, the tumors could be categorized<br />

into three groups: ordinary lipoma (n=16; 70%), oncocytic lipoadenoma<br />

(n=4) and non-oncocytic adenolipoma/sialolipoma (n=2). Ordinary lipomas<br />

were either completely intraglandular or they have been submitted<br />

as a lipomatous nodule containing minor foci of residual atrophic<br />

serous acini at the periphery of the lipoma beneath the capsule. None<br />

of the lipomas contained sebaceous elements or oncocytic cells. The less<br />

38 | Der Pathologe · Supplement 1 · 2012<br />

common oncocytic lipoadenoma (synonym: oncocytic sialolipoma) had<br />

a fatty component ranging from 10% to 95% of the lesion that was usually<br />

interspersed between the oncocytic acini. Sebaceous islands were found<br />

in three of the four cases. The oncocytes showed either diffuse solid<br />

sheets with a lobular architecture interrupted by scattered adipocytes<br />

or were scattered between plentiful fatty tissues. The two non-oncocytic<br />

adenolipoma (synonym: non-oncocytic sialolipoma) were predominantly<br />

fatty (70–80%) and prominently lobulated. They displayed a biphasic<br />

pattern with serous tissue diffusely distributed between the fatty components.<br />

One lesion showed foci of sebaceous metaplasia.<br />

Conclusions. Lipomatous tumors of the salivary glands are rare and most<br />

represent intraglandular ordinary lipomas that are otherwise similar<br />

to their soft tissue and cutaneous counterparts. While fairly absent in<br />

ordinary salivary lipomas, sebaceous differentiation seems to be a common<br />

feature of oncocytic lipoadenoma and non-oncocytic sialolipoma.<br />

Lipomatous lesions of the salivary glands do not seem to be association<br />

with other significant salivary gland pathology or to carry a risk of malignant<br />

degeneration. Although lipomatous components in these lesions<br />

might <strong>der</strong>ive from intraglandular adipose tissue, the pathogenesis of the<br />

oncocytic and sebaceous elements (metaplastic vs. neoplastic) remains<br />

unclear.<br />

AG Herz- und Gefäßpathologie<br />

DO-100<br />

microRNA-143 is essential in arteriogenesis<br />

K . Troidl1 , G . Jung1 , C . Troidl2 , W . Schaper 1 , T . Schmitz-Rixen3 1Max-Planck-Institute for Heart and Lung Research, Bad Nauheim,<br />

2 3 Kerckhoff Heart Centre, Bad Nauheim, Goethe University, Frankfurt<br />

Aims. Arteriogenesis – the growth of pre-existing collateral arterioles to<br />

functional arteries – is triggered by increased fluid shear stress (FSS).<br />

MicroRNAs (miRNA) are implicated in post-transcriptional regulation<br />

of gene expression. A FSS-induced signature pattern of miRNAs during<br />

collateral growth might influence signal transduction of the physical<br />

stimulus into a cellular response. We investigated the involvement of<br />

miRNAs in arteriogenesis in a rat model of chronically elevated FSS in<br />

collateral arteries.<br />

Methods. 6 sprague dawley rats were subjected to femoral artery ligature<br />

(FAL). A side-to-side anastomosis distal to the ligature was created<br />

between the femoral artery and the accompanying vein, which leads to<br />

chronically elevated FSS inside the collaterals. Following dissection of<br />

collateral tissue 7 d after surgery, miRNA was isolated and an expression<br />

profile was generated by microarray analysis. Differential expression was<br />

confirmed by qRT-PCR. Cellular localization of selected miRNAs was<br />

assessed by in situ hybridisation combined with immunostaining. By local<br />

blockage of specific miRNAs in mouse collaterals we analyzed their<br />

functional involvement in arteriogenesis.<br />

Results. Growing collaterals showed a significant up-regulation of 6<br />

miRNAs when compared to sham operated controls. miR-143, miR-195,<br />

and miR-24 were localized in the media of growing collaterals. miR-24 is<br />

also expressed in the FSS-stimulated endothelium. Blockage of miR-143<br />

led to severe impairment of arteriogenesis.<br />

Conclusions. These data indicate that miRNas are involved in arteriogenesis.<br />

miR-143 belongs to a cluster which has been assigned to the phenotypic<br />

switch of smooth muscle cells. We identified a functional implication<br />

during vascular remodeling. Targeted modulation of this miRNA<br />

in vivo suggests new treatment options in improvement of collateral<br />

growth.

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