Gheorghe Gabriela, Radu Oana, Milanovich Samuel, Hamilton Ronald L, Jaffe Ronald, Southern James F, Ozolek John A
Department of Pathology, Children's Hospital of Wisconsin, Medical College of Wisconsin, 9000 West Wisconsin Avenue, Milwaukee, WI 53226, USA.
Pediatr Dev Pathol. 2013 Mar-Apr;16(2):67-73. doi: 10.2350/12-01-1148-OA.1. Epub 2013 Jan 3.
Posttransplant lymphoproliferative disorders (PTLD) involving the central nervous system (CNS) in children are uncommon and can prove diagnostically challenging. The clinical and imaging characteristics of CNS PTLD can overlap with those of infection, hemorrhage, and primary CNS tumors. Some cases of CNS PTLD remain clinically unsuspected and are diagnosed postmortem. We report 6 instances of CNS PTLD in children, 2 of which were limited to the CNS and were unsuspected before autopsy. In our autopsy series, PTLD was found outside the CNS in 4 out of 6 cases. Since CNS PTLD has a poor prognosis and the presentation can be subtle, unsuspected, and high grade, it is important to maintain a high index of suspicion and to perform imaging and brain biopsy whenever clinically appropriate. In the presence of leptomeningeal involvement, the diagnosis could be made by cerebral spinal fluid examination.
儿童中枢神经系统(CNS)受累的移植后淋巴细胞增生性疾病(PTLD)并不常见,诊断具有挑战性。CNS PTLD的临床和影像学特征可能与感染、出血及原发性CNS肿瘤的特征重叠。一些CNS PTLD病例在临床上未被怀疑,尸检时才得以诊断。我们报告6例儿童CNS PTLD,其中2例局限于CNS,尸检前未被怀疑。在我们的尸检系列中,6例中有4例在CNS外发现PTLD。由于CNS PTLD预后不良,表现可能隐匿、未被怀疑且为高级别,因此保持高度怀疑指数并在临床适当时进行影像学检查和脑活检很重要。在存在软脑膜受累的情况下,可通过脑脊液检查做出诊断。