| Literature DB >> 34226971 |
Ichiro Kawashima1, Naoki Oishi2, Kazunari Kasai2, Tomohiro Inoue2, Eriko Hosokawa1, Ayato Nakadate1, Minori Matsuura1, Takuma Kumagai1, Megumi Koshiishi1, Takeo Yamamoto1, Kei Nakajima1, Masaru Tanaka1, Tetsuo Kondo2, Keita Kirito3.
Abstract
We report an exceptionally rare case of mantle cell lymphoma (MCL) that transdifferentiated into sarcoma with limited neuromuscular differentiation. An 81-year-old man with t(11;14)-positive MCL was treated with rituximab and bendamustine and achieved complete remission; however, just 2 months later, the patient developed multiple systemic tumors. Pathologic studies revealed round cell sarcoma expressing synaptophysin, CD56, and myogenin without any B-cell markers. The CCND1 translocation and an identical IGL gene rearrangement were shared by both the MCL and sarcoma. Whole-exome sequencing detected 189 single nucleotide variants (SNVs) in the MCL and 205 SNVs in the sarcoma; 160 SNVs including NSD2, ATM, RB1, and TP53 mutations were shared between MCL and sarcoma cells. An additional PTPN11 mutation was specifically found in the sarcoma. These findings confirmed the shared clonal origin of MCL and sarcoma in this patient and indicated that MCL can transdifferentiate into sarcoma in rare cases.Entities:
Keywords: ATM; CCND1; Mantle cell lymphoma; Sarcoma; TP53; Transdifferentiation
Mesh:
Year: 2021 PMID: 34226971 DOI: 10.1007/s00428-021-03148-9
Source DB: PubMed Journal: Virchows Arch ISSN: 0945-6317 Impact factor: 4.064