Ban Yoshihito, Tagawa Hiroshi, Wakatsuki Kai, Onishi Ryutaro, Noda Toshiyuki, Sugawara Masami, Ando Kumiko
Diagnostic Radiology, Kobe City Medical Center General Hospital, Kobe, JPN.
Pediatrics and Neonatology, Kobe City Medical Center General Hospital, Kobe, JPN.
Cureus. 2025 Jan 18;17(1):e77636. doi: 10.7759/cureus.77636. eCollection 2025 Jan.
Subpial hemorrhage is a rare type of birth-related brain hemorrhage in neonates that can manifest with symptoms such as apnea and seizures. On brain magnetic resonance imaging (MRI), subpial and parenchymal hemorrhages are typically observed but often resolve without lasting sequelae. Cytotoxic lesions of the corpus callosum (CLOCCs) are not as common in neonates as they are in adults and children. We present a rare case of a term neonate with subpial hemorrhage accompanied by CLOCCs who experienced a favorable clinical course. A full-term female infant was delivered via emergency cesarean section. At 18 hours post-birth, the infant experienced recurrent seizures. Following phenobarbital administration and the initiation of respiratory support, a brain MRI performed on day 6 revealed hematomas in the subpial and subcortical regions, leading to a diagnosis of subpial hemorrhage. Additionally, diffusion restriction was noted in the corpus callosum and optic radiation extending to the posterior limb. Follow-up MRI on day 14 of life showed the resolution of most of the lesions, confirming the diagnosis of CLOCCs. The infant was discharged on day 22 without further seizures and has shown normal growth and development for 18 months post-discharge. Thus, this case reports a neonatal patient with typical radiological features and clinical progression of subpial hemorrhage and CLOCCs, leading to a favorable outcome. The positive outcome underscores the importance of understanding the unique radiological features and progression of these conditions. In neonates presenting with splenial lesions associated with brain hemorrhage, it is crucial to monitor the resolution of symptoms and lesions to rule out alternative diagnoses. Furthermore, continued developmental monitoring is recommended to ensure optimal outcomes.
软脑膜下出血是新生儿中一种罕见的与出生相关的脑出血类型,可表现为呼吸暂停和癫痫发作等症状。在脑部磁共振成像(MRI)上,通常可观察到软脑膜下和实质内出血,但这些出血往往会自行消退,不留后遗症。胼胝体细胞毒性病变(CLOCCs)在新生儿中不如在成人和儿童中常见。我们报告了一例罕见的足月新生儿病例,该患儿患有软脑膜下出血并伴有CLOCCs,但临床过程良好。一名足月女婴通过急诊剖宫产出生。出生后18小时,该婴儿出现反复癫痫发作。在给予苯巴比妥并开始呼吸支持后,出生后第6天进行的脑部MRI显示软脑膜下和皮质下区域有血肿,从而诊断为软脑膜下出血。此外,在胼胝体和视辐射延伸至后肢处观察到扩散受限。出生后第14天的随访MRI显示大多数病变已消退,证实了CLOCCs的诊断。该婴儿在出生后第22天出院,未再出现癫痫发作,出院后18个月生长发育正常。因此,本病例报告了一名具有典型软脑膜下出血和CLOCCs放射学特征及临床病程的新生儿患者,最终获得了良好的结局。这一积极结果强调了了解这些病症独特放射学特征和病程的重要性。对于出现与脑出血相关的胼胝体病变的新生儿,监测症状和病变的消退情况以排除其他诊断至关重要。此外,建议持续进行发育监测以确保最佳结局。