Shafqat Areez, AlGethami Hanin Jaber, Shafqat Shameel, Islam Syed Shafqat Ul
College of Medicine, Alfaisal University, Riyadh, Kingdom of Saudi Arabia.
Division of Neurology, Department of Pediatrics, King Salman Hospital, Riyadh, Kingdom of Saudi Arabia.
Radiol Case Rep. 2022 Aug 5;17(10):3739-3744. doi: 10.1016/j.radcr.2022.07.055. eCollection 2022 Oct.
An 8-year-old boy presented to our hospital complaining of a bilateral headache associated with episodes of anterograde amnesia. He had a road traffic accident 3 years ago when a computed tomography (CT) scan revealed traumatic brain injury. In addition, a small pineal cyst (PC) was noted with minor intramural calcifications. A follow-up CT a day later demonstrated increased density in the pineal gland of 60 Hounsfield Units, suggestive of apoplectic changes in the PC. However, the patient was lost to follow-up and presented with memory loss a year and a half later, upon which CT and magnetic resonance imaging revealed enlargement of the PC. PC apoplexy is a very rare occurrence usually affecting young adult women; cases in children are rarely reported. Furthermore, PC apoplexy secondary to severe craniofacial trauma manifesting as memory loss has not yet been reported in the literature to the best of our knowledge.
一名8岁男孩因双侧头痛伴顺行性遗忘发作前来我院就诊。他3年前发生过道路交通事故,当时的计算机断层扫描(CT)显示有创伤性脑损伤。此外,还发现一个小的松果体囊肿(PC),伴有轻微的壁内钙化。一天后的随访CT显示松果体密度增加了60亨氏单位,提示PC有出血性改变。然而,该患者失访,一年半后出现记忆丧失,此时CT和磁共振成像显示PC增大。PC卒中非常罕见,通常影响年轻成年女性;儿童病例鲜有报道。此外,据我们所知,继发于严重颅面创伤并表现为记忆丧失的PC卒中在文献中尚未见报道。