Understanding kidney involvement in mycosis fungoides: T-cell clonality as a guide for targeted therapy - a case report and literature review.

IF 2.4 4区 医学 Q2 UROLOGY & NEPHROLOGY BMC Nephrology Pub Date : 2025-03-24 DOI:10.1186/s12882-025-04014-5
Jelena Filipović, Eve Maubec, Clelia Previtali, Milica Višić, Beatrice Villette, Gregory Lazarian, Remi Letestu, Joel Cucherousset, Michael Soussan, Antoine Martin
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Abstract

Background: Mycosis fungoides (MF) is a common T-cell lymphoma that primarily affects the skin. Renal involvement is rare and has never been reported as the initial extracutaneous site. T-cell clonality testing is essential for confirming systemic involvement. We report identical T-cell clonality in both the skin and renal involvement of MF, accompanied by a review of the literature on MF involvement in the kidneys.

Case presentation: A 58-year-old man with folliculotropic MF had asymptomatic bilateral kidney lesions incidentally detected on a routine magnet resonance imaging (MRI) 15 years after primary diagnosis. Immunohistochemistry (IHC) and polymerase chain reaction (PCR) confirmed clonal T-cell populations in skin and kidney biopsies, verifying systemic involvement. A Positron Emission Tomography (PET) scan showed a 50% reduction in kidney lesions after four months of therapy with Liposomal doxorubicin (20 mg/m2). However, despite this initial response, the disease spread to the lungs and pancreas, and the patient passed away eight months after kidney infiltration.

Conclusion: This is the first documented confirmation of MF involvement to the kidneys through specific IHC and T-cell PCR-confirmed clonality testing. It highlights advances in therapy for localized disease and underscores the importance of confirming T-cell clonality, especially in atypical sites like the kidneys, illustrating its potential to enhance targeted therapy in disseminated MF.

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了解蕈样真菌病的肾脏受累:t细胞克隆作为靶向治疗的指导-一个病例报告和文献综述。
背景:蕈样真菌病(MF)是一种常见的t细胞淋巴瘤,主要影响皮肤。肾脏受累是罕见的,从未报道过最初的皮外部位。t细胞克隆检测是确认系统性累及的必要条件。我们报告了MF的皮肤和肾脏受累的相同的t细胞克隆,并对MF在肾脏受累的文献进行了回顾。病例介绍:一名58岁男性嗜滤泡性MF患者在初次诊断15年后,在常规磁共振成像(MRI)中偶然发现无症状双侧肾脏病变。免疫组织化学(IHC)和聚合酶链反应(PCR)证实了皮肤和肾脏活检中的克隆t细胞群,证实了全身性病变。正电子发射断层扫描(PET)显示,用阿霉素脂质体(20mg /m2)治疗4个月后,肾脏病变减少了50%。然而,尽管最初有这种反应,但疾病扩散到肺部和胰腺,患者在肾脏浸润8个月后去世。结论:这是通过特异性免疫组化和t细胞pcr证实的克隆检测首次证实MF累及肾脏。它强调了局部疾病治疗的进展,并强调了确认t细胞克隆的重要性,特别是在肾脏等非典型部位,说明了其增强弥散性MF靶向治疗的潜力。
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来源期刊
BMC Nephrology
BMC Nephrology UROLOGY & NEPHROLOGY-
CiteScore
4.30
自引率
0.00%
发文量
375
审稿时长
3-8 weeks
期刊介绍: BMC Nephrology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of kidney and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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