PMID- 25511139 OWN - NLM STAT- MEDLINE DCOM- 20150213 LR - 20171116 IS - 1943-7722 (Electronic) IS - 0002-9173 (Linking) VI - 143 IP - 1 DP - 2015 Jan TI - Cytogenetic and flow cytometry evaluation of Richter syndrome reveals MYC, CDKN2A, IGH alterations with loss of CD52, CD62L and increase of CD71 antigen expression as the most frequent recurrent abnormalities. PG - 25-35 LID - 10.1309/AJCPATRQWANW2O3N [doi] AB - OBJECTIVES: Richter syndrome (RS) is a transformation of chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) into high-grade lymphoma. There are only limited data on flow cytometry (FCM) and cytogenetics in RS. METHODS: In this study, FCM, classic cytogenetics (CC), and fluorescence in situ hybridization (FISH) were performed in eight RS cases. RESULTS: Most cases of RS were characterized by a loss/decrease of CD52 and CD62L and increased CD71 expression. CC identified complex karyotypes, with losses of 9/9p and 17/17p as the most frequent in four of seven cases. Seven RS cases demonstrated MYC abnormalities. Disruptions of CDKN2A and IGH were identified in five of seven and four of seven RS cases, respectively. CONCLUSIONS: Newly diagnosed RS is an oncologic emergency, and a quick diagnostic decision is crucial in clinical practice. Therefore, in patients with CLL/SLL and rapidly enlarging asymmetric lymphadenopathy and/or extranodal tumors, we strongly advise FCM of fine-needle aspiration biopsy (FNAB) material, including CD62L, CD52, and CD71 analysis as well as assessment of karyotype and at least MYC abnormalities by FISH of the same FNAB material. Loss of CD52 expression in RS most likely predicts resistance to alemtuzumab therapy, which is frequently used in CLL. CI - Copyright(c) by the American Society for Clinical Pathology. FAU - Woroniecka, Renata AU - Woroniecka R AD - From the Cancer Genetics Laboratory and renatawr@coi.waw.pl. FAU - Rymkiewicz, Grzegorz AU - Rymkiewicz G AD - Flow Cytometry Laboratory of the Pathology Department and Laboratory Diagnostics, the Maria Sklodowska-Curie Memorial Institute and Cancer Centre, Warszawa, Poland; FAU - Grygalewicz, Beata AU - Grygalewicz B AD - From the Cancer Genetics Laboratory and. FAU - Blachnio, Katarzyna AU - Blachnio K AD - Flow Cytometry Laboratory of the Pathology Department and Laboratory Diagnostics, the Maria Sklodowska-Curie Memorial Institute and Cancer Centre, Warszawa, Poland; FAU - Rygier, Jolanta AU - Rygier J AD - From the Cancer Genetics Laboratory and. FAU - Jarmuz-Szymczak, Malgorzata AU - Jarmuz-Szymczak M AD - Department of Hematology and Bone Marrow Transplantation, University of Medical Sciences, Poznan, Poland; and Institute of Human Genetics, Polish Academy of Sciences, Poznan, Poland. FAU - Ratajczak, Blazej AU - Ratajczak B AD - Department of Hematology and Bone Marrow Transplantation, University of Medical Sciences, Poznan, Poland; and. FAU - Pienkowska-Grela, Barbara AU - Pienkowska-Grela B AD - From the Cancer Genetics Laboratory and. LA - eng PT - Journal Article PL - England TA - Am J Clin Pathol JT - American journal of clinical pathology JID - 0370470 RN - 0 (Antigens, CD) RN - 0 (Antigens, Neoplasm) RN - 0 (CD52 Antigen) RN - 0 (CD52 protein, human) RN - 0 (CD71 antigen) RN - 0 (Cyclin-Dependent Kinase Inhibitor p16) RN - 0 (Glycoproteins) RN - 0 (MYC protein, human) RN - 0 (Proto-Oncogene Proteins c-myc) RN - 0 (Receptors, Transferrin) RN - 126880-86-2 (L-Selectin) SB - IM MH - Adult MH - Aged MH - Antigens, CD/metabolism MH - Antigens, Neoplasm/metabolism MH - CD52 Antigen MH - Cyclin-Dependent Kinase Inhibitor p16/genetics/metabolism MH - Cytogenetic Analysis MH - Female MH - *Flow Cytometry MH - Genetic Testing/methods MH - Glycoproteins/deficiency/metabolism MH - Humans MH - L-Selectin/immunology MH - Leukemia, Lymphocytic, Chronic, B-Cell/*genetics/metabolism/pathology MH - Male MH - Middle Aged MH - Proto-Oncogene Proteins c-myc/metabolism MH - Receptors, Transferrin/metabolism OTO - NOTNLM OT - Alemtuzumab in CLL OT - CD52, CD62L, CD71 OT - Flow cytometry OT - MYC, CDKN2A, IGH OT - Richter syndrome EDAT- 2014/12/17 06:00 MHDA- 2015/02/14 06:00 CRDT- 2014/12/17 06:00 PHST- 2014/12/17 06:00 [entrez] PHST- 2014/12/17 06:00 [pubmed] PHST- 2015/02/14 06:00 [medline] AID - 143/1/25 [pii] AID - 10.1309/AJCPATRQWANW2O3N [doi] PST - ppublish SO - Am J Clin Pathol. 2015 Jan;143(1):25-35. doi: 10.1309/AJCPATRQWANW2O3N.