Shams Shadi, Issar Riddhima, Kadrmas-Iannuzzi Tanya
Medicine, Rowan School of Osteopathic Medicine, Stratford, USA.
Internal Medicine, Jefferson Health Washington Township, Turnersville, USA.
Cureus. 2022 Sep 10;14(9):e29009. doi: 10.7759/cureus.29009. eCollection 2022 Sep.
Ehlers-Danlos Syndrome (EDS), a rare genetic disorder, causes hyperlaxity, skin bruising, vascular disruption, and organ rupture. It presents with numerous complications, ranging from delayed gastric emptying to spontaneous rupture of blood vessels. A rare complication involves the neurological system and causes Tarlov cysts in the spinal canal. This gives rise to several symptoms, ranging from urinary and bowel incontinence to numbness and paresthesia. We report a case of an 11-year-old male with a past medical history of Ehlers-Danlos Syndrome, who presented with continued urinary and bowel incontinence, which was eventually found to be due to a Tarlov cyst. Although a handful of reports of Tarlov cysts exist in the literature, a presentation in a pediatric patient with a history of Ehlers-Danlos Syndrome is unconventional and unforeseen.
埃勒斯-当洛综合征(EDS)是一种罕见的遗传性疾病,会导致关节过度松弛、皮肤瘀伤、血管破裂和器官破裂。它会引发众多并发症,从胃排空延迟到血管自发性破裂不等。一种罕见的并发症累及神经系统,导致椎管内出现塔尔洛夫囊肿。这会引发多种症状,从大小便失禁到麻木和感觉异常。我们报告一例11岁男性患者,有埃勒斯-当洛综合征病史,出现持续的大小便失禁,最终发现是由一个塔尔洛夫囊肿所致。尽管文献中有一些关于塔尔洛夫囊肿的报道,但在一名有埃勒斯-当洛综合征病史的儿科患者中出现这种情况并不常见且出乎意料。