A Rare Case of Plasmablastic Myeloma After Renal Transplant.

IF 0.7 4区 医学 Q4 TRANSPLANTATION
Sabir Sulejman, Ardian Memeti, Vlora Sadiku, Galina Severova, Gazmend Amzai, Nikola Gjorgjievski, Gordana Petrushevska, Goce Spasovski
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Abstract

Posttransplant lymphoproliferative disorders are a serious complication after solid-organ transplant, with a reported incidence from 2% to 20%. Plasma cell neoplasms in solid-organ transplants represent a rare but increasingly serious complication after solid-organ transplant. We report a case of plasmablastic myeloma, a very rare variant of multiple myeloma with aggressive course and poor prognosis. Few such cases have been reported in the literature in patients after solid-organ transplant. A 41-year-old male patient received a renal transplant from a living unrelated donor (wife) in 2019. After transplant, he was given triple immunosuppression therapy (mycophenolic acid, tacrolimus, prednisolone). In September 2024, 56 months after transplant, the patient presented to our nephrology department due to confusion, weight loss, loss of appetite, and gastric discomfort. Laboratory results showed hypercalcemia, elevated serum creatinine, and thrombocytopenia with anemia, without apparent blood loss. As a result of persistent hypercalcemia and elevated serum creatinine levels, treatment with hemodialysis was initiated. Polymerase chain reaction results were negative for Epstein-Barr virus. After preliminary preparation, bone marrow biopsy was performed, which revealed infiltration by cells with blastic morphology. Immunohistochemical analysis confirmed the finding with more than 80% of cells positive for CD138; the remaining marker tests were mostly negative. The day after the bone marrow biopsy, the patient had progressive deterioration in his health, with severe malaise and disorientation; he developed acute heart failure and pulmonary edema. An urgent hemodialysis was initiated, but it was unsuccessful. The patient died on day 10 of hospitalization. Posttransplant lymphoproliferative disorders and other malignant neoplasms pose a serious posttransplant complication in patients with challenging diagnoses due to overlapping features with other posttransplant complications; such patients most often experience a rapid and atypical course, due to high doses of immunosuppressants.

肾移植后发生浆母细胞骨髓瘤1例。
移植后淋巴增生性疾病是实体器官移植后的严重并发症,据报道发病率为2%至20%。实体器官移植后浆细胞肿瘤是一种罕见但日益严重的并发症。我们报告一例浆母细胞骨髓瘤,一种非常罕见的多发性骨髓瘤变种,病程积极,预后差。文献中很少报道固体器官移植后患者出现这种情况。一名41岁的男性患者在2019年接受了非亲属活体捐赠者(妻子)的肾脏移植手术。移植后给予三联免疫抑制治疗(霉酚酸、他克莫司、强的松龙)。2024年9月,移植后56个月,患者因意识模糊、体重减轻、食欲不振、胃部不适来到我肾内科就诊。实验室结果显示高钙血症,血清肌酐升高,血小板减少伴贫血,无明显失血。由于持续高钙血症和血清肌酐水平升高,开始进行血液透析治疗。聚合酶链反应结果对eb病毒呈阴性。初步准备后,行骨髓活检,发现有胚状细胞浸润。免疫组织化学分析证实了这一发现,超过80%的细胞CD138阳性;其余的标记测试大多为阴性。骨髓活检后第二天,患者健康状况进行性恶化,出现严重的不适和定向障碍;他出现了急性心力衰竭和肺水肿。紧急进行了血液透析,但没有成功。患者于住院第10天死亡。移植后淋巴增生性疾病和其他恶性肿瘤由于与其他移植后并发症的重叠特征,对诊断具有挑战性的患者构成严重的移植后并发症;由于高剂量的免疫抑制剂,这类患者通常经历快速和非典型病程。
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来源期刊
CiteScore
1.40
自引率
11.10%
发文量
258
审稿时长
6-12 weeks
期刊介绍: The scope of the journal includes the following: Surgical techniques, innovations, and novelties; Immunobiology and immunosuppression; Clinical results; Complications; Infection; Malignancies; Organ donation; Organ and tissue procurement and preservation; Sociological and ethical issues; Xenotransplantation.
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