Simultaneous deletion of 3′ETV6 and 5′EWSR1 genes in blastic plasmacytoid dendritic cell neoplasm: case report and literature review

Background Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare hematologic malignancy. Based on literature reports of limited cases, over 50 % of BPDCN have chromosomal abnormalities, but no single chromosomal change has been identified as diagnostic of this entity. Case presentation In this report, we present a case of BPDCN with complicated chromosomal abnormalities involving chromosomes 12 and 22 and resulting in a simultaneous partial deletion of ETV6 and EWSR1. Notably, these aberrations were identified in bone marrow myeloid precursors in the absence of bone marrow involvement by BPDCN. Conclusion Analysis of 46 BPDCN cases with abnormal karyotypes (45 from literature reports plus this case) showed that 12p- is one of the most common structural aberrations in BPDCN. The ETV6 and CDKN1B on 12p deserve further investigations as potential markers of BPDCN.

In this report, we present a case of BPDCN with complicated chromosomal abnormalities involving chromosomes 12 and 22 and resulting in simultaneous partial deletion of ETV6 and EWSR1. These findings were identified in the BM of a patient with BPDCN in the absence of morphologic, immunohistochemical, or flow cytometry evidence of BPDCN. We also conduct a literature review of conventional cytogenetic findings in BPDCN.

Case presentation
The patient is a previously healthy 44-year-old man who presented with a painless enlarging mass in his left groin. He was observed initially for three months and eventually was referred for an excisional lymph node biopsy. Histologic examination showed a highgrade malignant neoplasm that was diagnosed as BPDCN. He was then referred to our institution. BM evaluation included a trephine biopsy and aspiration. There was no evidence of BPDCN in BM by morphology or immunohistochemistry. Flow cytometry was also negative for BPDCN in BM. However, conventional cytogenetic analysis performed on the BM aspirate sample showed karyotypic aberrations involving chromosomes 12 and 22, which were further characterized by fluorescence in situ hybridization (FISH) analysis (see details below). The patient was treated with a hyper-CVAD-Bortezomib regimen (hyperfractioned cyclophosphamide, vincristine, doxorubicin, dexamethasone alternating with high dose of methotrexate and cytarabine, plus bortezomib) regimen. He also received prophylactic intrathecal chemotherapy with methotrexate for 3 cycles and achieved a complete remission.

Conventional chromosomal analysis
Conventional chromosomal analysis (karyotyping) was performed on G-banded metaphase cells prepared from unstimulated 24-h and 48-h bone marrow cultures as described previously [7]. Twenty metaphases (10 from each culture) were analyzed. The chromosomal abnormalities were reported according to the International System for Human Cytogenetic Nomenclature 2013 (ISCN2013) guidelines [8]. Out of 20 metaphases analyzed, 10 exhibited structural abnormalities involving chromosomes 12 and 22.

Fluorescence in situ Hybridization (FISH) analysis
The following FISH probes were applied in this study: Vysis ETV6 Break Apart (BAP) FISH probe and Vysis EWSR1 BAP FISH probe (Abbott Molecular, Des Plaines, IL) were used for interphase, metaphase and tissue FISH tests. The Vysis MYC BAP FISH probe (Abbott Molecular, Des Plaines, IL) was used for both interphase and tissue FISH tests. The Vysis LSI BCR/ABL ES Dual Color Fusion probe (Abbott Molecular, Des Plaines, IL) was used for interphase FISH tests, whereas the Aquarius Whole Chromosome Painting (WCP) probes for chromosomes 12 and 22 (Cytocell, Tarrytown, NY) were used for metaphase FISH only. All probes were thoroughly validated in accordance with the American College of Medical Genetics and Genomics (ACMGG) guidelines.
Interphase FISH performed on unstimulated cultured cells from BM sample using the ETV6 BAP probe showed that about 25 % of cells had a one-red-one-fusion (1R1F) signal pattern, indicating an ETV6 gene rearrangement with a partial deletion of the 3′ETV6 (green signal). A separate interphase FISH analysis using the EWSR1 BAP probe showed that almost the same percentage of cells had a one-green-one-fusion (1G1F) signal pattern, demonstrating an EWSR1 gene rearrangement with a partial deletion of the 5′EWSR1 (red signal). Mapping back to previously G-banded and karyotyped metaphases showed that the existing 5′ETV6 (red signal) is located at the long arm of the abnormal chromosome 22, whereas the existing 3′EWSR1 (green signal) is located at the short arm of the abnormal chromosome 12 (Fig. 1). Whole chromosome painting (WCP) further confirmed the origins as abnormal chromosomes 12 and 22 (images not shown). Therefore, the results of conventional cytogenetic analysis and FISH analysis suggest that a translocation between 12p and 22q occurred. This was likely followed by a pericentric inversion of the abnormal chromosome 12 resulting in a partial deletion of both 3′ETV6 and 5′EWSR1. These two abnormal chromosomes are described as der(12)t(12;22)(p13;q12)del(22)(q12q12)inv(12)(p13q24.1) and der(22)t(12;22)del(12)(p13p13).
Due to the complexity of these chromosomal aberrations and a low resolution of the available karyogram, the derivative chromosomes were drawn by using the online CyDAS software [9], and the corresponding FISH signals were labeled (Fig. 2). Neither MYC gene rearrangement nor BCR/ABL fusion were detected in the BM specimen.
Interphase FISH performed on the formalin-fixed, paraffin-embedded LN sample showed that 90 % of cells had the same EVT6 and EWSR1 signal patterns as detected in the BM (images not shown). Therefore, the same chromosomal aberrations have been confirmed on FFPE tissues of the LN biopsy as well. We combined morphologic and FISH analysis as described previously [10,11] to further characterize the type of BM cells carrying the chromosomal aberrations described above. As shown in Fig. 3, all cells in the BM specimen were morphologically and immunopheno typically normal (Fig. 3a, H.E. staining image), but FISH tests using ETV6 BAP probe on the same slide detected a positive signal pattern for ETV6 rearrangement and partial deletion of 3′ETV6 (Fig. 3b, FISH test image).

Molecular testing
The BM sample was screened for somatic mutations using a clinically validated next-generation sequencing (NGS)based 28-gene assay [6].

Discussion
We report the first case of BPDCN that carried a translocation between chromosomes 12 and 22, followed by a subsequent pericentric inversion of the abnormal chromosome 12, and that resulted in a simultaneous partial deletion of 3′ETV6 and 5′EWSR1. Based on separate locations of the remaining 5′ETV6 and 3′EWSR1 (Fig. 2), there is unlikely an ETV6/EWSR1 fusion gene present in this case. Importantly, these aberrations were detected in BPDCN cells in the LN as well as in hematopoietic precursors in a BM samples that had no evidence of involvement by BPDCN.
The cytogenetic characterization of BPDCN is not well established, mostly due to the rarity of this disease and its relatively recent recognition and diagnostic characterization. In one of the largest cohorts to date, Leroux et al. [4] reported that 14 of 21 cases of CD4 + CD56+ DC2 acute leukemia/BPDCN had an abnormal karyotype, which was further characterized using interphase FISH, metaphase FISH, whole chromosome painting (WCP) and spectral karyotyping (SKY). These analyses delineated six major chromosomal targets for this disease, including 5q (72 %), 12p (64 %), 13q (64 %), 6q (50 %), 15q (43 %) and 9 (28 %). Additional smaller studies and reports showed similar findings.
In Table 1, we have summarized a total of 46 BPDCN cases with abnormal karyotypes, 45 from previous literature reports [4,6,[12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28] plus the case presented in this report. A minor modification has been made to some of the cases from previous literature reports in order to follow the ISCN 2013 nomenclature guidelines [8] as well as to integrate all findings derived by means other than conventional analysis (e.g., FISH and SKY) into the description of an abnormal karyotype. A similar number of BPDCN cases with possible chromosomal abnormalities are not included in this table, mainly due to a lack of complete karyotype description in these literature [29][30][31][32][33][34][35][36][37]. In addition, our analysis has focused on cytogenetic alterations and does not include mutations in genes such as TET2 that have been shown to be present in a sizeable subset of BPDCN [6,38]. The mutational landscape of BPDCN is beyond the scope of this review.
Thirty-four of 46 (74 %) cases of BPDCN reported had a complex karyotype (at least 3 chromosomal aberrations including at least one structural aberration), indicating that multiple recurrent chromosomal abnormalities are very common. The frequency of involvement of each chromosome is listed in Table 2. Of interest, our literature review identified the same six major chromosomal aberrancies reported by Leroux et al. [4], but with a deviant frequency for each chromosome as follows: 6 (20/46, 43 %), 12 (  Leroux et al. [4] 3 84~87,XX,del(X)(q24),del(X)(q24),add(2)(q3?),der(2)(?),+del(4)(q23),+del(5)(q14),+del(5) (q14q23),add(6)(q?),-9,-11,del (12) Karube et al. [20] aberrations were detected frequently for chromosomes 13 (18/20, 90 %), 9 (12/17, 71 %) and 15 (9/17, 53 %), we observed structural aberrations more commonly in chromosomes 6 (20/20, 100 %), 5 (14/15, 93 %) and 12 (16/20, 80 %). Further analysis examining the breakpoints and consequences of the above mentioned structural aberrations has revealed that 5q-, 6q-and/or 12p-were common with a frequency of 93 % for 5q-, 90 % for 6q-, and 88 % for 12p-. This phenomenon has been observed by Lucioni et al. [29] in a study of 21 BPDCN cases by using an array-based comparative genomic hybridization (aCGH) assay as well as by other research groups [5,[30][31][32][33][34]. We have an ongoing project studying the correlation between the complexity of the karyotype and outcome of this disease in patients who had been seen and followed-up in our institute. The 12p-is considered to be one of the most common structural aberrations in BPDCN. Two major target genes/loci located on the 12p have been identified as potential hotspots in the literature, CDKN1B and ETV6. The CDKN1B gene is located on 12p13.1p12 spanning from 12,717,270 to 12,722,383 (5114 bp, GRCh.38.p2). The protein encoded by this gene, p27 (also known as KIP1), is a kinase inhibitor and an atypical tumor suppressor through regulation of the activity of cyclin-dependent kinases (Cdks). Therefore, dysfunction of CDKN1B plays a role in pathogenesis and metastasis of multiple cancers, such as breast cancer, prostate cancer and leukemia [39]. Loss of the CDKN1B locus has been reported in over 60 % of BPDCN cases, including cases with a normal karyotype [5,[29][30][31][32]. Due to the size of this gene, its loss has been detected only by array comparative genomic hybridization assay in the literature. Immunohistochemistry studies have further confirmed weak expression of p27 protein in almost all these cases. ETV6, also known as TEL, THC5 or TEL/ABL gene, is located on 12p13 spanning from 11,649,854 to 11,895,402 (245,549 bp), less than 1 Mb apart from CDKN1B. Both genes were simultaneously lost in the cases mentioned above. ETV6 is a gene with the characteristics of a tumor suppressor gene and encodes an ETS family transcription factor. ETV6 has been shown to play an important role in the pathogenesis of various types of leukemia, mostly through forming fusion genes with over 40 different translocation partners [40,41]. In BPDCN (Tables 1 and 2), over 40 % of cases had a structural abnormality involving 12p, very likely resulting in a 12p-at various breakpoints and including a deletion of CDKN1B and ETV6 in most cases by roughly analyzing the breakpoints. Some of these cases might have had an ETV6 rearrangement as well. ETV6 (approximately 250 Kb of size) is a good target for FISH testing and other studies have demonstrated a deletion or rearrangement of ETV6 by FISH testing in BPDCN cases with or without an obvious 12p-; the deletion can be monoallelic or biallelic [5,29]. Therefore, 12p-, more specifically a deletion or rearrangement of CDKN1B and/or ETV6, may deserve further investigations as potential markers of BPDCN.
In summary, over 50 % of BPDCN cases have chromosomal abnormalities, with more than 70 % of BPDCN cases exhibiting a complex karyotype. Monosomy 13/ 13q-, 12p-, 6q-, monosomy 15/15q-, 5q-and monosomy 9 are characteristic chromosomal abnormalities in BPDCN. The 12p-is one of the most common structural aberrations in BPDCN, and a deletion/rearrangement of CDKN1B and/or ETV6 on 12p is often detected. These two genes, together with EWSR1 on 22q, may deserve further investigations as potential BPDCN markers.

Consent
Written informed consent was obtained from the patient for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.