| Literature DB >> 32785819 |
Yuichi Sumii1, Noboru Asada2, Yasuharu Sato3,4, Koh-Ichi Ohshima5, Masanori Makita6, Yusuke Yoshimoto7, Yuka Sogabe8, Kenji Imajo6, Yusuke Meguri1, Daisuke Ennishi1, Hisakazu Nishimori1, Nobuharu Fujii9, Ken-Ichi Matsuoka1, Tadashi Yoshino4, Yoshinobu Maeda1.
Abstract
IgG4-producing marginal zone B-cell lymphomas (MZLs) have been recently proposed as a subtype of MZLs. Despite the abundant literature on pathophysiological features of this type of lymphoma, only a few retrospective studies pertaining to the treatment outcomes have been reported, and its prognosis remains unclear. We retrospectively analyzed seven patients with IgG4-producing MZLs diagnosed at our institute, with specific reference to treatment and outcomes. The median age was 69.0 years (55-79), and all were males. The median follow-up period was 66.6 months (8-121). All patients had localized disease; four patients had tumors of the ocular adnexa, whereas two had retroperitoneal tumors. Five patients were treated with irradiation (30 Gy/15 fr) (n = 4) or surgery (n = 1), resulting in tumor reduction. Two patients were treated by chemotherapy or irradiation. Among them, one commenced rituximab monotherapy, which led to an inadequate reduction of the tumor. Subsequent irradiation induced complete response (CR). The other patient experienced repeated relapses during follow-up and finally achieved CR by combination chemotherapy. Treatment was well tolerated in all cases, and none of the patients showed disease progression at the last follow-up visit. Our results indicate that the standard treatments for MZLs are generally appropriate for IgG4-producing MZL.Entities:
Keywords: Extranodal marginal zone B-cell lymphoma; IgG4; IgG4-related disease
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Year: 2020 PMID: 32785819 DOI: 10.1007/s12185-020-02968-w
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490