Case Report: ABO-incompatible living donor liver transplantation in a patient with associated Rosai-Dorfman-Destombes disease, first reported case.

Frontiers in transplantation Pub Date : 2025-04-24 eCollection Date: 2025-01-01 DOI:10.3389/frtra.2025.1576301
Bhabani Sankar Sahoo, Kausar Makki, Vikas Saini, Piyush Srivastava, Vivek Vij
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Abstract

Rosai-Dorfman-Destombes disease (RDD), a rare histiocytic proliferation, is often associated with lymphadenopathy and extranodal manifestations, including involvement of the liver. We report a unique case of RDD presenting with chronic liver disease (CLD) in a 7-year-old boy, highlighting the association between these conditions. The patient underwent ABO-incompatible living donor liver transplantation (LDLT), a procedure not previously documented in the context of RDD. Successful transplantation was preceded by a desensitization protocol including rituximab and immunoadsorption, and was followed by a satisfactory postoperative course. This case underscores the need for further investigation into the relationship between RDD and CLD and the potential of LDLT as a life-saving treatment option in such complex cases.

病例报告:abo血型不相容的活体供肝移植一例伴有伴有Rosai-Dorfman-Destombes病的患者,首次报道。
Rosai-Dorfman-Destombes病(RDD)是一种罕见的组织细胞增生,常伴有淋巴结病变和结外表现,包括累及肝脏。我们报告一个独特的病例RDD表现为慢性肝病(CLD)在一个7岁的男孩,突出这些条件之间的关联。患者接受了abo血型不相容的活体供体肝移植(LDLT),这是一种以前没有在RDD背景下记录的手术。移植成功之前进行了包括利妥昔单抗和免疫吸附在内的脱敏治疗,随后进行了令人满意的术后治疗。该病例强调需要进一步调查RDD和CLD之间的关系,以及LDLT作为这种复杂病例中挽救生命的治疗选择的潜力。
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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