Appiani Franco E, Claverie Carlos S, Klein Francisco R
Universitat Internacional de Catalunya Barcelona Spain.
Neurology Department Favaloro University Hospital Buenos Aires Argentina.
Clin Case Rep. 2024 Jul 31;12(8):e9100. doi: 10.1002/ccr3.9100. eCollection 2024 Aug.
Posterior Reversible Encephalopathy Syndrome, typically characterized by parieto-occipital vasogenic edema, can present atypically, as a bilateral symmetrical vasogenic edema in the basal ganglia, featuring the called "lentiform fork sign." Prompt recognition of such variations is crucial for accurate diagnosis and tailored management, highlighting the complexity of this syndrome's manifestations.
Posterior Reversible Encephalopathy Syndrome (PRES) manifests as transient neurological symptoms and cerebral edema, commonly associated with immunosuppressive drugs (ISDs) in transplant recipients. ISDs can lead to endothelial dysfunction and compromise the blood-brain barrier. Typically, PRES exhibits identifiable MRI patterns, often demonstrating vasogenic edema in the bilateral parieto-occipital white matter. Identifying unique presentations, such as the recently observed "lentiform fork sign," commonly seen in uremic encephalopathy, emphasizes this syndrome's broad spectrum manifestations. A 19-year-old male, who underwent bilateral lung and liver transplantation, experienced a bilateral tonic-clonic seizure of unknown onset 47 days post-surgery. MRI findings revealed an unconventional PRES pattern, featuring the "lentiform fork sign" as bilateral symmetrical vasogenic edema in the basal ganglia, surrounded by a hyperintense rim outlining the lentiform nucleus bilaterally. Subsequent management, including ISD modification and magnesium supplementation, resulted in clinical and neuroimaging resolution. An almost complete clinical and radiological resolution was achieved after 14 days. The occurrence of PRES in transplant recipients highlights the intricate interplay among ISDs, physiological factors, and cerebrovascular dynamics, potentially involving direct neurovascular endothelial toxicity and disruption of the blood-brain barrier. Neuroimaging plays a pivotal role in diagnosis. The distinctive "lentiform fork sign" was observed in this patient despite the absence of typical metabolic disturbances. Management strategies usually involve reducing hypertension, discontinuing ISDs, correcting electrolyte imbalances, and initiating antiseizure drugs if necessary. Identifying the presence of the "lentiform fork sign" alongside typical PRES edema in a patient lacking renal failure emphasizes that this manifestation is not solely indicative of uremic encephalopathy. Instead, it might represent the final common pathway resulting from alterations in the blood-brain barrier integrity within the deep white matter. Understanding such atypical imaging manifestations could significantly aid earlier and more precise diagnosis, influencing appropriate management decisions.
后部可逆性脑病综合征通常以顶枕部血管源性水肿为特征,但也可能表现不典型,如基底节区双侧对称性血管源性水肿,即所谓的“豆状核叉征”。及时识别这些变异对于准确诊断和个性化治疗至关重要,凸显了该综合征临床表现的复杂性。
后部可逆性脑病综合征(PRES)表现为短暂性神经症状和脑水肿,在移植受者中通常与免疫抑制药物(ISD)有关。ISD可导致内皮功能障碍并损害血脑屏障。通常,PRES在MRI上呈现可识别的模式,常显示双侧顶枕部白质血管源性水肿。识别独特的表现,如最近观察到的、常见于尿毒症脑病的“豆状核叉征”,强调了该综合征广泛的临床表现。一名19岁男性,接受了双侧肺和肝移植,术后47天出现不明原因的双侧强直阵挛性发作。MRI检查结果显示一种非典型的PRES模式,以基底节区双侧对称性血管源性水肿即“豆状核叉征”为特征,双侧豆状核周围有高信号环勾勒出轮廓。随后的治疗,包括调整ISD和补充镁,使临床症状和神经影像学表现得到缓解。14天后实现了几乎完全的临床和影像学缓解。移植受者中PRES的发生凸显了ISD、生理因素和脑血管动力学之间复杂的相互作用,可能涉及直接的神经血管内皮毒性和血脑屏障破坏。神经影像学在诊断中起关键作用。尽管该患者没有典型的代谢紊乱,但仍观察到独特的“豆状核叉征”。治疗策略通常包括控制高血压、停用ISD、纠正电解质失衡以及必要时启动抗癫痫药物治疗。在缺乏肾衰竭的患者中识别出“豆状核叉征”以及典型的PRES水肿,强调这种表现并非仅提示尿毒症脑病。相反,它可能代表深部白质血脑屏障完整性改变所导致的最终共同途径。了解这些非典型影像学表现可显著有助于更早、更准确的诊断,影响适当的治疗决策。