Bhoil Amit, RacuAmoasii Igor, Vinjamuri Sobhan
Department of Nuclear Medicine, The Royal Liverpool University Hospital NHS Trust, Liverpool, United Kingdom.
Haemato-oncology Diagnostic Service, Liverpool Clinical Laboratories, Liverpool, United Kingdom.
World J Nucl Med. 2022 Sep 9;22(1):29-32. doi: 10.1055/s-0042-1757253. eCollection 2023 Mar.
Primary central nervous system lymphomas (PCNSLs) are extranodal variant forms of non-Hodgkin lymphoma arising within the brain parenchyma, leptomeninges, or spinal cord. PCNSL can present with varied neurological symptoms and imaging findings, making diagnosis without biopsy difficult. PCNSLs are highly aggressive, causing rapid deterioration, but are responsive to chemotherapy and radiotherapy making early diagnosis important. Crossed cerebellar diaschisis (CCD) is mostly seen with cerebral cortex vascular insults and is rarely reported with thalamic lesions and even rarer with thalamic lymphoma. However, CCD has also been described in other brain tumors (including primary glioma), chronic subdural hematoma, congenital insults, intracranial infections, and various dementia subtypes. We present a rare case of thalamic lymphoma evaluated with positron emission tomography/computed tomography that showed hypermetabolism of thalamus and associated hypometabolism in ipsilateral cerebral cortex and contralateral cerebellum representing CCD.
原发性中枢神经系统淋巴瘤(PCNSLs)是起源于脑实质、软脑膜或脊髓的非霍奇金淋巴瘤的结外变异形式。PCNSL可表现出多种神经症状和影像学表现,使得在无活检的情况下难以诊断。PCNSL具有高度侵袭性,可导致病情迅速恶化,但对化疗和放疗有反应,因此早期诊断很重要。交叉性小脑失联络(CCD)多见于大脑皮质血管损伤,丘脑病变报道较少,丘脑淋巴瘤则更为罕见。然而,CCD也在其他脑肿瘤(包括原发性胶质瘤)、慢性硬膜下血肿、先天性损伤、颅内感染及各种痴呆亚型中被描述。我们报告1例罕见的丘脑淋巴瘤病例,经正电子发射断层扫描/计算机断层扫描评估,显示丘脑代谢增高,同侧大脑皮质和对侧小脑代谢减低,提示CCD。