Department of Respiratory Medicine, Beijing Children's Hospital, Capital Medical University, Nanlishi Road 56, Xicheng District, Beijing, China.
Department of Pathology, Beijing Children's Hospital, Capital Medical University, Nanlishi Road 56, Xicheng District, Beijing, China.
Orphanet J Rare Dis. 2019 Feb 8;14(1):35. doi: 10.1186/s13023-019-1009-5.
Primary pulmonary lymphoma (PPL) is a rare disease, especially in children. We analyse the clinical features of PPL in 4 children to strengthen a understanding of it.
We reported a case series of 4 pediatric patients with PPLs including three diffuse large B-cell lymphomas and one natural killer-T cell lymphoma. All patients presented with unknown fever and cough as well as weight loss and fatigue. The white blood cell count was reduced in three patients and increased in the other one. The level of C-reactive protein was increased in all patients. The procalcitonin concentrations and bone marrow specimens were normal. Multiple or single pulmonary nodules with halo signs were found in all patients and air bronchograms found in 3 of them on chest computed tomography scan. Primary immunodeficiency was diagnosed in two patients who was performed genetic analysis.
When a patient presents with long-term fever, high C-reactive protein level, leukopenia/leukocytosis, and multiple or single pulmonary nodules with a "halo sign" and air bronchogram on computed tomography, a possibility of PPL should be considered. A co-existance of immunodeficiency needs to be further investigated in patients with PPL.
原发性肺淋巴瘤(PPL)是一种罕见疾病,尤其在儿童中较为少见。我们分析了 4 例儿童 PPL 的临床特征,以加强对此病的认识。
我们报告了 4 例儿科 PPL 患者的病例系列,包括 3 例弥漫性大 B 细胞淋巴瘤和 1 例自然杀伤 T 细胞淋巴瘤。所有患者均表现为不明原因的发热、咳嗽,以及体重减轻和乏力。3 例患者的白细胞计数减少,1 例患者的白细胞计数增加。所有患者的 C 反应蛋白水平升高。降钙素原浓度和骨髓标本均正常。所有患者的胸部 CT 扫描均显示多个或单个肺结节伴晕征,3 例患者显示空气支气管征。2 例患者诊断为原发性免疫缺陷,并进行了基因分析。
当患者出现长期发热、高 C 反应蛋白水平、白细胞减少/增多和多个或单个肺结节伴“晕征”和 CT 上的空气支气管征时,应考虑 PPL 的可能性。对于 PPL 患者,需要进一步调查是否存在免疫缺陷共存。