Kontny H U, Sleasman J W, Kingma D W, Jaffe E S, Avila N A, Pizzo P A, Mueller B U
Pediatric Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-1182, USA.
J Pediatr. 1997 Aug;131(2):264-70. doi: 10.1016/s0022-3476(97)70164-1.
Children with human immunodeficiency virus (HIV) infection have an increased susceptibility to severe and unusual infections, malignancies, and disorders characterized by abnormal lymphoproliferation (e.g., lymphoid interstitial pneumonitis). We report a novel disease entity associated with pediatric HIV infection that is characterized by massive enlargement of the thymus as a result of lymphoid hyperplasia and multicystic changes.
Eight patients with HIV infection and cystic enlargement of the thymus are subject of this report. The status of their HIV disease and its clinical and radiologic manifestations at the time of diagnosis of the mediastinal mass are described. Tissue specimens were obtained from six patients and examined by microscopy and immunohistochemistry. The specimens were also evaluated for the evidence of HIV and Epstein-Barr virus by in situ hybridization.
Patients were between 2.1 and 12.1 years of age, with CD4+ cell counts between 102 and 733 cells/mm3. In all eight cases an anterior mediastinal mass was discovered incidentally on radiography of the chest, and computed tomography of the chest revealed a multicystic appearance. Histologic examination demonstrated distortion of the thymic architecture by focal cystic changes, lymphoid follicular hyperplasia, diffuse plasmacytosis, and multinucleated giant cells. In situ hybridization revealed HIV particles on the surface of follicular dendritic cells. Further, results of in situ hybridization for EBV were positive in lymphoid cells from biopsy samples of four patients. The patients were followed between 8 months and 4.8 years. In five patients the mass either decreased in size or resolved completely.
We describe a series of children with HIV infection and multilocular thymic cysts. We hypothesize that aberrant immunoregulation in these HIV-infected children leads to follicular hyperplasia and multicystic changes in the thymus, causing massive enlargement. EBV infection might also contribute to the pathogenesis of this process. Because none of our patients had symptoms from the mass, and there was no evidence of malignancy in the examined biopsy samples, it seems prudent to manage such children with careful follow-up examinations.
感染人类免疫缺陷病毒(HIV)的儿童更容易发生严重和罕见的感染、恶性肿瘤以及以异常淋巴增殖为特征的疾病(如淋巴样间质性肺炎)。我们报告了一种与儿童HIV感染相关的新型疾病实体,其特征是由于淋巴样增生和多囊性改变导致胸腺大量肿大。
本报告以8例HIV感染且胸腺呈囊性肿大的患者为研究对象。描述了他们在诊断纵隔肿块时的HIV疾病状况及其临床和影像学表现。从6例患者身上获取组织标本,进行显微镜检查和免疫组织化学检测。还通过原位杂交评估标本中HIV和爱泼斯坦-巴尔病毒(EBV)的证据。
患者年龄在2.1至12.1岁之间,CD4 +细胞计数在102至733个细胞/mm³之间。在所有8例病例中,胸部X线检查偶然发现前纵隔肿块,胸部计算机断层扫描显示为多囊性外观。组织学检查显示胸腺结构因局灶性囊性改变、淋巴滤泡增生、弥漫性浆细胞增多和多核巨细胞而扭曲。原位杂交显示滤泡树突状细胞表面有HIV颗粒。此外,4例患者活检样本的淋巴细胞中EBV原位杂交结果为阳性。对患者进行了8个月至4.8年的随访。5例患者的肿块大小减小或完全消退。
我们描述了一系列HIV感染且胸腺有多房囊肿的儿童。我们推测这些HIV感染儿童的免疫调节异常导致胸腺滤泡增生和多囊性改变,从而引起胸腺大量肿大。EBV感染也可能促成这一过程的发病机制。由于我们的患者均无肿块相关症状,且在检查的活检样本中没有恶性肿瘤的证据,对这类儿童进行仔细的随访检查似乎是谨慎的做法。