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

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Abstracts<br />

than the diffuse pattern. Similar results could be found concerning<br />

the FOXP3 cells and the infiltration pattern. The nodular pattern had<br />

significant more reactive FOXP3 positive cells than the diffuse pattern<br />

(p=0.018). High number of CD8 cells were found in patients with lower<br />

leucocytes counts (p=0.049) and higher lymphocytes double time (more<br />

than 12 months, p=0.048). All other correlation between clinical, biological<br />

and genetic correlation with T-cells accounts shows no significant<br />

differences.<br />

Conclusions. Lymph node biopsies with B-CLL had a significant higher<br />

account of T-cells than bone marrow biopsies. Patients with B-CLL and<br />

a nodular bone marrow involvement had a significant higher number of<br />

CD3+ and FOXP+ T-Cells. High numbers of CD8+ T-cells cells might<br />

have a positive influence on the lymphocytes double time and leukocytes<br />

level at the time of diagnosis.<br />

FR-P-159<br />

Collision lymphomas in the bone marrow – a diagnostic pitfall<br />

A .M . May1 , L . Morawietz2 , W . Dietrich3 , A . Lindemann4 , G . Faller 5 , P . Fisch1 ,<br />

M . Werner1 1University Freiburg Medical Center, Institute of Pathology, Freiburg,<br />

2 3 Klinikum Stuttgart, Institute of Pathology, Stuttgart, Klinikum Stuttgart,<br />

Stuttgart, 4Oncologic Practice, Ettlingen, 5St . Vincentius-Kliniken, Institute of<br />

Pathology, Karlsruhe<br />

Aims. The simultaneous co-existence of two distinct lymphoma entities<br />

in one bone marrow trephine biopsy (BMB) is rare and can be easily missed,<br />

especially in cases with a high density of infiltration. We present the<br />

cases of two patients with a compact infiltrate in the BMB, which turned<br />

out be composed of two different kinds of lymphoma.<br />

Methods. The distinct lymphoma entities in these two patients’ BMB<br />

were extensively analyzed, using immunohistochemistry and a PCR-based<br />

clonality analysis of immunoglobulin heavy chain gene rearrangements.<br />

Results. One patient’s BMB was infiltrated by hairy cell leukemia (infiltration<br />

density: 75%). In a lymph node biopsy that had been examined separately,<br />

due to a conspicuous abdominal lymphadenopathy, mantle cell<br />

lymphoma was diagnosed. Further studies provided a minimal presence<br />

of mantle cell lymphoma cells in the BMB as well as a discrete population<br />

of hairy cells in the lymph node biopsy. Clonality analysis of the immunoglobulin<br />

heavy chain gene identified two distinct clonal B-cell populations.<br />

In the other patient’s BMB an unusual gigantocellular variant of<br />

B-lymphoblastic lymphoma was diagnosed. The immunohistochemical<br />

analysis indicated a diagnosis of cALL. Flow cytometric analyses found<br />

two separate, but only discrete B-cell populations in the peripheral blood<br />

and bone marrow. One of these populations was immature; the other<br />

population was suspicious of mantle cell lymphoma. Subsequent immunohistochemistry<br />

showed a minute additional presence of mantle cell<br />

lymphoma in the BMB.<br />

Conclusions. In case of clinically unusual presentation, additional examinations,<br />

such as more extensive immunohistochemistry, molecular<br />

methods and flow cytometric analyses, need to be included into the<br />

diagnostic spectrum of lymphomas, to be able to identify rare cases of<br />

collision lymphomas.<br />

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

FR-P-160<br />

Primary gastric ALK-negative anaplastic large cell lymphoma:<br />

a clinicopathologic analysis of four cases<br />

C . Liu1 , Y . Lai1 , X . Wang1 , X . Huang1 , M . Li1 , Z . Gao1 1Peking University Health Science Center, Beijing, China<br />

Aims. To evaluate clinicopathological and immunophenotypic features<br />

of primary gastric ALK-negative anaplastic large cell lymphomas<br />

(ALCLs).<br />

Methods. Formalin-fixed, paraffin embedded tissue blocks of 4 patients<br />

diagnosed with primary gastric ALK-negative ALCL were obtained. Hematoxylin<br />

and Eosin-stained slides were used to evaluate histological<br />

changes and the immunophenotypic features were detected by immunohistochemistry.<br />

In addition, the abnormality of ALK gene was determined<br />

by interphase fluorescence in situ hybridization (FISH).<br />

Results. The cases were comprised of three men and one woman, with<br />

a median age of 58.5 years. All the four cases presented with epigastric<br />

discomfort with or without gastrorrhagia. Endoscopic examination<br />

revealed solitary gastric ulcer in all cases. Endoscopic biopsy from one<br />

patient and surgical specimens from three patients were available. Morphologically,<br />

the normal architecture of gastric wall was effaced by the<br />

diffuse infiltration of tumor cells, in which the characteristic hallmark<br />

cells were easily identified in all cases. The tumor cells of all cases showed<br />

a consistently strong expression of CD30 but lack of the expression<br />

of ALK1. Moreover, the tumor cells demonstrated varying expression of<br />

T cell markers such as CD3 (3/4) and CD43 (1/1), and negative for B-cell<br />

markers CD20 and PAX5. Chromosomal rearrangement involving ALK<br />

gene was not detected by FISH. Three of the four cases un<strong>der</strong>went total<br />

or partial gastrectomy followed by chemotherapy and till the last followup;<br />

none of them developed a relapse or progression. The rest one patient<br />

refused surgery and chemotherapy, and died 20 months after diagnosis.<br />

Conclusions. Here we reported four ALK-negative ALCLs occurred in<br />

the stomach. Although it’s a rare condition, we should keep in mind<br />

to avoid misdiagnosis especially of the gastric carcinoma. The current<br />

results suggested that ALK-negative ALCL may have a good prognosis<br />

with surgery combined with chemotherapy.<br />

Poster: Autopsie/Fallstudien/Sonstiges<br />

FR-P-161<br />

Postmortem CT in clinical autopsy<br />

S . Westphal1 , J . Apitzsch2 , T . Penzkofer2 , A . Perez-Bouza 1 , B . Sellhaus3 ,<br />

A . Mahnken2 , R . Knüchel-Clarke1 1 2 RWTH Aachen University, Institute of Pathology, Aachen, RWTH Aachen<br />

University, Department of Interventional and Diagnostic Radiology, Aachen,<br />

3RWTH Aachen University, Institute of Neuropathology, Aachen<br />

Aims. While autopsy rates in clinical pathology are declining for the past<br />

decades, and forensic sciences are using virtual autopsy techniques increasingly<br />

in daily routine, pathologists are not yet tapping the potential<br />

of mo<strong>der</strong>n imaging techniques. To assess the value of virtual autopsy<br />

techniques in clinical pathology, post- mortem imaging was performed<br />

before autopsy.<br />

Methods. In 29 autopsy cases, a full-body high-definition pmCT (postmortem<br />

computed tomography) scan was performed prior to autopsy.<br />

Images were analyzed by experienced radiologists. Autopsy was performed<br />

following a standard protocol, taking special care of macroscopical<br />

findings, detected in the CT scan previously. Digital macroscopical<br />

pictures of the organs and of their histology were taken. We compared<br />

pmCT and classical autopsy findings regarding cause of death and death-related<br />

diagnoses, reconstruction of the key pathomechanism leading<br />

to death and side diagnoses.

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