Patel Harsh D, Nevah Rubin Moises I
McGovern Medical School, Department of Internal Medicine, The University of Texas Health Science Center at Houston, 6431 Fannin St., Suite MSB 1.134, Houston, TX 77030, USA.
McGovern Medical School, Department of Gastroenterology, Transplant and Advanced Hepatology, The University of Texas Health Science Center at Houston, 6431 Fannin St., Suite MSB 1.134, Houston, TX 77030, USA.
Case Rep Hematol. 2017;2017:7247438. doi: 10.1155/2017/7247438. Epub 2017 Sep 11.
Posttransplant lymphoproliferative disorder (PTLD) is a spectrum of diseases that involves abnormal lymphoid and/or plasmacytic proliferation in patients with solid organ or hematopoietic cell transplantation. It is a condition with a low incidence of 3.5-4.3% in liver transplant (LT) recipients. This case involves a 63-year-old male with history of LT for chronic HCV induced cirrhosis who presented with abdominal distension related to worsening ascites. Cytological ascitic fluid analysis revealed EBV (+) malignant cells without a malignant focal point on imaging. Diagnosis of monomorphic PTLD with primary effusion lymphoma-like morphology and immunophenotype was established. This case highlights the complexity in diagnosis, different diagnostic modalities, and rare clinical presentations of PTLD.
移植后淋巴增殖性疾病(PTLD)是一系列疾病,涉及实体器官或造血细胞移植患者的异常淋巴样和/或浆细胞增殖。在肝移植(LT)受者中,其发病率较低,为3.5 - 4.3%。该病例为一名63岁男性,有因慢性丙型肝炎病毒(HCV)引起的肝硬化而接受肝移植的病史,因腹水恶化出现腹胀。腹水细胞学分析显示EBV(+)恶性细胞,影像学上无恶性病灶。确立了具有原发性渗出性淋巴瘤样形态和免疫表型的单形性PTLD的诊断。该病例突出了PTLD诊断的复杂性、不同的诊断方式以及罕见的临床表现。