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A Violaceous Nodule in a Lung-transplant Patient

机译:肺移植患者的紫癜性结节

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Posttransplantation lymphoproliferative disorder (PTLD) is a rare complication of solid organ or allogenic bone marrow transplantation. Cases localized to the skin are even rarer, with only around 100 cases recorded in the literature [2]. We present a case of 60 year-old-woman, a lung transplant recipient, who presented with an asymptomatic violaceous nodule on her left medial calf. Histopathology was consistent with PTLD of the B-cell subtype, EBV negative. This case is unique in that it was of the B cell subtype of cutaneous PTLD, which has been less commonly observed than the T cell subtype. In addition, the case was EBV negative, which is rare in B cell cutaneous PTLD. The patient was treated with rituximab 600 mg IV weekly for four weeks and cytomegalovirus immune globulin (Cytogam) 100 mg/kg once, with resolution of the nodule.
机译:移植后淋巴细胞增生性疾病(PTLD)是实体器官或同种异体骨髓移植的罕见并发症。局限于皮肤的病例甚至更少,文献中仅记录了约100例[2]。我们介绍了一例60岁的女性,一名肺移植受者,在她的左小腿内侧出现了无症状的紫胶结节。组织病理学与B细胞亚型的PTLD一致,EBV阴性。这种情况是独特的,因为它是皮肤PTLD的B细胞亚型,这种情况比T细胞亚型少见。另外,该病例为EBV阴性,这在B细胞皮肤PTLD中很少见。该患者每周接受600 mg利妥昔单抗静脉输注治疗四周,一次巨细胞病毒免疫球蛋白(Cytogam)100 mg / kg,结节消退。

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