Epstein-Barr virus-associated post-transplant smooth muscle tumours in a kidney transplant patient.

IF 2.6 3区 医学 Q1 PEDIATRICS
Pediatric Nephrology Pub Date : 2025-02-01 Epub Date: 2024-09-04 DOI:10.1007/s00467-024-06493-4
Carlos J Cobeñas, Priscila Pereyra, Ana Paula Spizzirri, Cristina Gauto Santacruz, Angela Del Carmen Suarez, Eugenia Altamirano, Paula Pérez, Nicolas Tello
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Abstract

We report on a 14-year-old girl who developed post-transplantation smooth muscle tumours (PTSMT) located in the spleen, lungs, liver, and central nervous system (CNS), 4 years after kidney transplantation. She was asymptomatic, and the disease was detected during the work-up for a urinary tract infection. Diagnosis was performed by the analysis of a tissue specimen, through the biopsy of a lung tumour, which revealed a proliferation of spindle-shaped cells which were positive for actin and vimentin. In situ hybridization studies were positive for Epstein-Barr virus, and her serologic status was negative prior to transplantation. We reduced immunosuppression by stopping mycophenolate and switching tacrolimus for sirolimus. After 18 months of follow-up, she remains asymptomatic, and the CNS tumour reduced its diameter from 24 × 21 mm to 14 × 13 mm. PTSMT should be considered in the differential diagnosis of transplanted patients who develop neoplastic complications associated with immunosuppression.

Abstract Image

一名肾移植患者的移植后平滑肌瘤与 Epstein-Barr 病毒有关。
我们报告了一名 14 岁女孩在接受肾移植 4 年后出现移植后平滑肌瘤(PTSMT)的病例,肿瘤位于脾脏、肺、肝脏和中枢神经系统(CNS)。她没有任何症状,是在一次尿路感染的检查中被发现的。诊断是通过肺部肿瘤活检组织标本分析得出的,标本显示有纺锤形细胞增生,肌动蛋白和波形蛋白呈阳性。原位杂交研究显示爱泼斯坦-巴氏病毒呈阳性,而移植前她的血清学状态为阴性。我们停止使用霉酚酸酯,将他克莫司换成西罗莫司,从而减少了免疫抑制。经过18个月的随访,她仍然没有任何症状,中枢神经系统肿瘤的直径也从24×21毫米缩小到14×13毫米。对于出现与免疫抑制相关的肿瘤性并发症的移植患者,在鉴别诊断时应考虑 PTSMT。
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来源期刊
Pediatric Nephrology
Pediatric Nephrology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
20.00%
发文量
465
审稿时长
1 months
期刊介绍: International Pediatric Nephrology Association Pediatric Nephrology publishes original clinical research related to acute and chronic diseases that affect renal function, blood pressure, and fluid and electrolyte disorders in children. Studies may involve medical, surgical, nutritional, physiologic, biochemical, genetic, pathologic or immunologic aspects of disease, imaging techniques or consequences of acute or chronic kidney disease. There are 12 issues per year that contain Editorial Commentaries, Reviews, Educational Reviews, Original Articles, Brief Reports, Rapid Communications, Clinical Quizzes, and Letters to the Editors.
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