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Erschienen in: Annals of Hematology 10/2018

12.06.2018 | Original Article

Diagnosis of Richter transformation in chronic lymphocytic leukemia: histology tips the scales

verfasst von: Birgit Federmann, Martin R. Mueller, Julia Steinhilber, Marius S. Horger, Falko Fend

Erschienen in: Annals of Hematology | Ausgabe 10/2018

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Abstract

Development of diffuse large B-cell lymphoma in chronic lymphocytic leukemia, so-called Richter transformation (RT), occurs in 2–5% of patients and is associated with poor outcome. The clinical features of RT are fairly non-specific and unable to discriminate transformation from other mimics. In case of clinically suspected RT, a CT/MRT is recommended, and FDG-PET/CT may help to select the site of biopsy. Radiological features suggestive of RT have been defined, but there are only limited data about their predictive value, and histological confirmation is still considered the gold standard for RT diagnosis. We retrospectively analyzed 34 patients with clinically suspected RT and available radiological and histological data. A histopathological diagnosis of RT with concordant clinical and radiological findings was obtained in 13 patients. In 18 patients, CT did not show features of transformation, concordant with lack of RT in the biopsy. Of interest, a distinct lymphoma other than DLBCL was identified in two of these cases. A false-positive radiological diagnosis of RT was rendered in two patients, including a case of Herpes simplex virus lymphadenitis. In conclusion, our findings confirm the central role of tissue biopsy in the diagnostic work up in case of clinically suspected RT.
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Metadaten
Titel
Diagnosis of Richter transformation in chronic lymphocytic leukemia: histology tips the scales
verfasst von
Birgit Federmann
Martin R. Mueller
Julia Steinhilber
Marius S. Horger
Falko Fend
Publikationsdatum
12.06.2018
Verlag
Springer Berlin Heidelberg
Erschienen in
Annals of Hematology / Ausgabe 10/2018
Print ISSN: 0939-5555
Elektronische ISSN: 1432-0584
DOI
https://doi.org/10.1007/s00277-018-3390-x

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