A RARE CASE OF A RESISTANT EXTRANODAL FOLLICULAR LYMPHOMA WITH PLASMACYTIC DIFFERENTIATION TRANSFORMED IN DIFFUSE LARGE B CELL LYMPHOMA TREATED SUCCESSFULLY WITH AUTOLOGOUS BONE MARROW TRANSPLANTATION.

IF 1.8 Q3 HEMATOLOGY
Viola CAVOLLI , Aferdita UKIMERAJ , Suzana KRASNIQI
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Abstract

Case report: Context

The incidence of extranodal presentation of the disease is less than 10% in follicular lymphomas. Follicular lymphoma with plasmacytic differentiation arising in an extranodal site like subcutaneous tissue and bone is uncommon and its natural history and treatment are poorly described in the literature.

Objective

Sharing an unusual case report of a resistant extranodal follicular lymphoma with plasmacytic differentiation transformed in Diffuse Large B Cell lymphoma ABC subtype undergoing successful treatment with bone marrow transplantation.

Case report

In November 2012 a 48-year-old woman was complaining about knee pain during movements. A CT done at that time demonstrated an osteolytic lesion in her right knee in the lateral condyle. The biopsy of the lesion was consistent with the diagnosis of follicular lymphoma with plasmocytic differentiation. Bone marrow aspiration and total body CT were normal without evidence of other tumor masses. The patient underwent radiation therapy and was in perfect condition until late 2017 when she was presented to the hematology consultation because of some subcutaneous masses on her body. PET CT scan revealed several subcutaneous masses with high FDG uptake, one in her right shoulder (3.5 × 1.8 cm), two on her right breast (6.0 × 3.4 cm and 2.1 × 1.3 cm), one on the left side of her neck (1.5 × 0.6 cm), and one on her left inguinal region (4.0 × 2.3 cm). A biopsy of the mass in her inguinal region revealed the diagnosis of follicular lymphoma with plasmacytic differentiation (CD10, CD20, CD138, and MUM1 positive). She was referred to the hematology department for further evaluation and treatment. On admission, the bone marrow aspiration and biopsy showed no malignant diseases. Due to the perfect clinical condition of the patient, we decided to go with Rituximab monotherapy. But after 4 courses no improvement was seen. So, we decided to go with RCVP therapy but still, the disease was refractory, and the PET CT showed other than the subcutaneous masses, a lytic bone lesion in her left talus. We went with 2 RCHOP therapies and 4 RCHOEP plus Bortezomib and only after that, the patient went into total remission. One year later, the masses started to grow in the same location. A second biopsy revealed high-grade follicular lymphoma. We continued with R-lenalidomide but the disease was still refractory. A third biopsy performed showed a high-grade DLBCL ABC subtype. In this condition, we started salvage therapy with 2 cycles of R-BEGEV protocol and referred the patient to a clinic abroad for autologous bone marrow transplantation. The patient underwent total remission after the protocol and autologous bone marrow transplant. She has been in remission since July 2022.

Discussion

The transformation of follicular lymphoma with plasmacytic differentiation, positive for MUM1 has a high probability according to literature to be resistant to standard therapy and to progress to diffuse large B cell lymphoma ABC subtype. Therefore, the need for aggressive treatment combined with bone marrow transplantation is important.

一例罕见的具有浆液性分化的耐药结节外滤泡淋巴瘤,经自体骨髓移植成功治疗后转变为弥漫大 B 细胞淋巴瘤。
病例报告:背景:在滤泡性淋巴瘤中,结节外淋巴瘤的发病率不到10%。目的分享一例罕见的结节外滤泡性淋巴瘤病例报告,该病具有浆液性分化,并转化为弥漫大 B 细胞淋巴瘤 ABC 亚型,经骨髓移植治疗后获得成功。当时所做的 CT 显示,她的右膝外侧髁有一处溶骨性病变。病变活检结果与滤泡性淋巴瘤(浆细胞分化型)的诊断一致。骨髓穿刺和全身CT检查结果正常,未发现其他肿瘤肿块。患者接受了放疗,情况一直很好,直到2017年底,她因身上出现一些皮下肿块而到血液科就诊。正电子发射计算机断层扫描(PET CT)发现了几个高FDG摄取的皮下肿块,其中一个在右肩(3.5 × 1.8厘米),两个在右乳(6.0 × 3.4厘米和2.1 × 1.3厘米),一个在左侧颈部(1.5 × 0.6厘米),一个在左侧腹股沟区(4.0 × 2.3厘米)。对腹股沟区的肿块进行活检后发现,诊断结果为浆液性分化的滤泡性淋巴瘤(CD10、CD20、CD138 和 MUM1 阳性)。她被转到血液科接受进一步评估和治疗。入院时,骨髓穿刺和活检均未发现恶性疾病。鉴于患者的临床状况良好,我们决定采用利妥昔单抗单药治疗。但 4 个疗程后,病情未见好转。正电子发射计算机断层扫描显示,除了皮下肿块外,她的左侧距骨还出现了溶解性骨病变。我们采用了 2 种 RCHOP 疗法和 4 种 RCHOEP 加硼替佐米疗法,之后患者的病情才完全缓解。一年后,肿块开始在同一位置生长。第二次活组织检查发现了高级别滤泡性淋巴瘤。我们继续使用 R-来那度胺,但病情仍然难治。第三次活检显示为高级别DLBCL ABC亚型。在这种情况下,我们开始了2个周期的R-BEGEV方案挽救治疗,并将患者转诊到国外一家诊所进行自体骨髓移植。在接受方案治疗和自体骨髓移植后,患者的病情得到了完全缓解。根据文献报道,浆液性分化的滤泡性淋巴瘤转化为 MUM1 阳性后,极有可能对标准治疗产生耐药性,并进展为弥漫大 B 细胞淋巴瘤 ABC 亚型。因此,积极治疗并结合骨髓移植非常重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
4.80%
发文量
1419
审稿时长
30 weeks
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