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 />
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.