Abstract
Histiocytic sarcoma (HS) is a rare aggressive hematologic neoplasm that can be associated with low-grade B cell lymphoma. The development of both neoplasms is currently being considered a transdifferentiation mechanism but remains elusive. We report the case of a 65-year-old patient with synchronous development of peritoneal/abdominal HS and grade 1–2 follicular lymphoma (FL). Cytogenetic analysis and targeted next-generation sequencing of both FL and HS tumors identified common genomic alterations such as IGH-BCL2 rearrangement, CREBBP and KMT2D, and aberrations of chromosomes 9q and 19q. However, only the HS tumor had a KRAS mutation while the lymph node involved by FL harbored a TNFAIP3 mutation and both tumors also showed distinct chromosomal alterations. This report strengthens the hypothesis of a common lymphoid progenitor which accumulates genetic alterations leading to two different hematologic malignant diseases with significantly distinct prognoses.
Abbreviations
- CLL:
-
Chronic lymphocytic leukemia
- CNV:
-
Copy number variation
- FL:
-
Follicular lymphoma
- HS:
-
Histiocytic sarcoma
- LCN:
-
Langerhans cell neoplasm
- LDH:
-
Lactate dehydrogenase
- MCL:
-
Mantle cell lymphoma;
- NMZL:
-
Nodal marginal zone lymphoma
- SMZL:
-
Splenic marginal zone lymphoma
References
Shao H, Xi L, Raffeld M, Feldman AL, Ketterling RP, Knudson R et al (2011) Clonally related histiocytic/dendritic cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma: a study of seven cases. Mod Pathol Off J U S Can Acad Pathol Inc 24:1421–1432
Ambrosio MR, De Falco G, Rocca BJ, Barone A, Amato T, Bellan C, et al. (2015) Langerhans cell sarcoma following marginal zone lymphoma: expanding the knowledge on mature B cell plasticity. Virchows Arch Int J Pathol467:471–480
Wang E, Hutchinson CB, Huang Q, Sebastian S, Rehder C, Kanaly A, et al. (2010) Histiocytic sarcoma arising in indolent small B-cell lymphoma: report of two cases with molecular/genetic evidence suggestive of a “transdifferentiation” during the clonal evolution. Leuk Lymphoma51:802–812
Hure MC, Elco CP, Ward D, Hutchinson L, Meng X, Dorfman DM, Yu H (2012) Histiocytic sarcoma arising from clonally related mantle cell lymphoma. J Clin Oncol Off J Am Soc Clin Oncol 30:e49–e53
Bassarova A, Trøen G, Fosså A, Ikonomou IM, Beiske K, Nesland JM, et al. (2009) Transformation of B cell lymphoma to histiocytic sarcoma: somatic mutations of PAX-5 gene with loss of expression cannot explain transdifferentiation. J Hematop2:135–141
Brunner P, Rufle A, Dirnhofer S, Lohri A, Willi N, Cathomas G, et al. (2014) Follicular lymphoma transformation into histiocytic sarcoma: indications for a common neoplastic progenitor. Leukemia28:1937–1940
Feldman AL, Arber DA, Pittaluga S, Martinez A, Burke JS, Raffeld M, et al. (2008) Clonally related follicular lymphomas and histiocytic/dendritic cell sarcomas: evidence for transdifferentiation of the follicular lymphoma clone. Blood111:5433–5439
Fernandez-Pol S, Bangs CD, Cherry A, Arber DA, Gratzinger D (2016) Two cases of histiocytic sarcoma with BCL2 translocations and occult or subsequent follicular lymphoma. Hum Pathol55:39–43
Mehrotra S, Pan Z (2015) Fine needle aspiration cytology of histiocytic sarcoma with dendritic cell differentiation: a case of transdifferentiation from low-grade follicular lymphoma. Diagn Cytopathol43:659–663
West DS, Dogan A, Quint PS, Tricker-Klar ML, Porcher JC, Ketterling RP, et al. (2013) Clonally related follicular lymphomas and Langerhans cell neoplasms: expanding the spectrum of transdifferentiation. Am J Surg Pathol37:978–986
Zeng W, Meck J, Cheson BD, Ozdemirli M (2011) Histiocytic sarcoma transdifferentiated from follicular lymphoma presenting as a cutaneous tumor. J Cutan Pathol38:999–1003
Zhang D, McGuirk J, Ganguly S, Persons DL (2009) Histiocytic/dendritic cell sarcoma arising from follicular lymphoma involving the bone: a case report and review of literature. Int J Hematol89:529–532
Stoecker MM, Wang E (2013) Histiocytic/dendritic cell transformation of B-cell neoplasms: pathologic evidence of lineage conversion in differentiated hematolymphoid malignancies. Arch Pathol Lab Med137:865–870
Swerdlow SH, Campo E, Pileri SA, Harris NL, Stein H, Siebert R, et al.( 2016) The 2016 revision of the World Health Organization classification of lymphoid neoplasms. Blood127:2375–2390
Hung YP, Lovitch SB, Qian X (2017) Histiocytic sarcoma: new insights into FNA cytomorphology and molecular characteristics. Cancer Cytopathol125:604–614
Weigert O, Weinstock DM (2017) The promises and challenges of using gene mutations for patient stratification in follicular lymphoma. Blood 130:1491–1498
Zehir A, Benayed R, Shah RH, Middha S, Kim HR, Srinivasan P et al (2017) Mutational landscape of metastatic cancer revealed from prospective clinical sequencing of 10,000 patients. Nat Med 23:703–713
Liu Q, Tomaszewicz K, Hutchinson L, Hornick JL, Woda B, Yu H (2016) Somatic mutations in histiocytic sarcoma identified by next generation sequencing. Virchows Arch Int J Pathol469:233–241
Acknowledgments
We thank Pr Pierre Brousset, Dr. Nathalie Van Acker, and Dr. Juliet Raine for reviewing the report, Dr. Marine Borel for contributing to collect sample, Frederic Escudié and David Grand for contributing to the targeted next-generation DNA sequencing, and the Institut Universitaire de France who supported this study.
Funding
This study was funded by the Institut Universitaire du Cancer de Toulouse, the Labex TOUCAN.
Author information
Authors and Affiliations
Contributions
S Péricart, C Vaysse, C Laurent, and S Evrard collected samples and data. S Péricart, A Siegfried, S Evrard, and C Laurent analyzed the data and wrote the paper. E Delabesse and S Evrard performed and analyzed targeted next-generation DNA sequencing. S Struski performed and analyzed cytogenetic analysis. All authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Ethics approval and consent to participate Tissue samples were collected at the CRB biobank (DC-2008-463 and transfer agreement AC-2008-820) and processed following standard ethical procedures (Helsinki Declaration of 1975) after obtaining written informed consent from the patient. The study was approved by the local ethical committee (Comité de Protection des Personnes Sud-Ouest et Outremer II). For cytogenetics analysis, fresh and thawed samples from the patient were obtained after informed consent and stored at the HIMIP (INSERM-Midi Pyrénées Malignant Blood Diseases collection). According to the French law, the HIMIP collection was declared to the Ministry of Higher Education and Research (DC 2008-307 collection 1) for which a transfer agreement (AC 2008-129) was obtained after approbation by the ethical committee (CPP). Clinical and biological annotations of the samples were declared to the CNIL (Comité National Informatique et Libertés ie Data processing and Liberties National Committee).
Conflict of interest
The authors declare that they have no conflict of interest.
Disclaimer
The opinions, results, and conclusions reported in this paper are those of the authors and are independent of the funding sources. No endorsement by Institute Universitaire de Cancer de Toulouse is intended or should be inferred. Parts of this material are based on data and/or information compiled and provided by the Institute Universitaire de Cancer de Toulouse. However, the analyses, conclusions, opinions, and statements expressed in the material are those of the author(s), and not necessarily those of Institute Universitaire de Cancer de Toulouse.
Additional information
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Rights and permissions
About this article
Cite this article
Péricart, S., Waysse, C., Siegfried, A. et al. Subsequent development of histiocytic sarcoma and follicular lymphoma: cytogenetics and next-generation sequencing analyses provide evidence for transdifferentiation of early common lymphoid precursor—a case report and review of literature. Virchows Arch 476, 609–614 (2020). https://doi.org/10.1007/s00428-019-02691-w
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00428-019-02691-w