Zhu Fang, Li Qiuhui, Liu Tao, Xiao Yin, Pan Huaxiong, Liu Xinxiu, Wu Gang, Zhang Liling
Cancer Center.
Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Medicine (Baltimore). 2020 Aug 28;99(35):e21844. doi: 10.1097/MD.0000000000021844.
The heart transplantation is the most important treatment for patients with end-stage severe heart disease who failed to conventional therapy. Post-transplant lymphoproliferative disorder is the second most common malignancy in heart transplant recipients. However, primary central nervous system lymphoma (PCNSL) after heart transplantation is an extremely rare condition.
This report described a 53-year-old male who was diagnosed as PCNSL 17 months after heart transplantation.
The patient was admitted to the local hospital presenting with dizziness, headache, and reduced left-sided power and sensation for 1 week. He had a medical history of heart transplantation because of the dilated cardiomyopathy 17 months ago and had a 17-month history of immunosuppressive therapy with tacrolimus. A computed tomography scan of the brain revealed a bulky mass in the right temporal lobe. The emergency intracranial mass resection and cerebral decompression were performed in our hospital. The histopathology of the brain lesions showed diffuse large B-cell lymphoma. A further FDG positron emission tomography-computed tomography scan of the whole body showed no significantly increased metabolic activity in other regions. The final diagnosis of this patient was PCNSL after heart transplantation.
Given the poor health condition, with the patient's consent, the whole brain radiotherapy was performed with supportive care.
The disease deteriorated rapidly during the period of receiving radiotherapy, and he died within 2 months from the diagnosis.
PCNSL after heart transplantation is an extremely rare phenomenon with extremely poor prognosis. We should pay close attention to the heart recipients, especially when the patients present with neurological symptoms and signs. The available treatment options for PCNS-post-transplant lymphoproliferative disorder include the reduction of immunosuppressive drugs, immune-chemotherapy, operation, radiotherapy. However, individual treatments for heart transplant recipients with PCNSL should be based on the performance status and tolerance to treatment, combined with the doctor's experience and supportive care.
心脏移植是终末期重症心脏病患者经传统治疗无效后的最重要治疗手段。移植后淋巴组织增生性疾病是心脏移植受者中第二常见的恶性肿瘤。然而,心脏移植后原发性中枢神经系统淋巴瘤(PCNSL)极为罕见。
本报告描述了一名53岁男性,在心脏移植17个月后被诊断为PCNSL。
患者因头晕、头痛、左侧肢体力量和感觉减退1周入住当地医院。他有17个月前因扩张型心肌病接受心脏移植的病史,接受他克莫司免疫抑制治疗17个月。脑部计算机断层扫描显示右侧颞叶有一个巨大肿块。我院进行了急诊颅内肿块切除术和脑减压术。脑病变的组织病理学显示为弥漫性大B细胞淋巴瘤。进一步的全身氟代脱氧葡萄糖正电子发射断层扫描-计算机断层扫描显示其他区域代谢活性无明显增加。该患者最终诊断为心脏移植后PCNSL。
鉴于患者健康状况较差,在患者同意下,给予全脑放疗并进行支持治疗。
放疗期间病情迅速恶化,自诊断起2个月内死亡。
心脏移植后PCNSL是一种极其罕见的现象,预后极差。我们应密切关注心脏移植受者,尤其是当患者出现神经症状和体征时。移植后淋巴组织增生性疾病相关PCNSL的可用治疗选择包括减少免疫抑制药物、免疫化疗、手术、放疗。然而,心脏移植受者PCNSL的个体化治疗应基于其身体状况和对治疗的耐受性,并结合医生的经验和支持治疗。