Gantait Varaha Venkat, Paul Imon, Jamil Adnan, Das Anamika
Department of Psychiatry, IQ City Medical College and Hospital, Durgapur, West Bengal, India.
Indian J Psychiatry. 2024 Jun;66(6):581-584. doi: 10.4103/indianjpsychiatry.indianjpsychiatry_983_23. Epub 2024 Jun 19.
Kleine Levin syndrome (KLS) is a rare entity. It presents with subacute onset episodic hypersomnia, cognitive decline, altered perception, and occasional hyperphagia and hypersexuality with full recovery during the interepisodic period. Five cases presented with episodic hypersomnia and met the diagnostic criteria of KLS. The majority of the cases were females (3/5) in whom KLS is even rarer. The initial presentation was in the age range of 10-25 years. Cognitive dysfunction (5/5), derealization (4/5), viral prodrome (3/5), hyperphagia (3/5), and hypersexuality (2/5) were other clinical presentations. A differential diagnosis of atypical depression is the major challenge, and thorough history taking would help in differentiation. Treatment with stimulants (modafinil) and mood stabilizers (lithium) proved effective. A high degree of suspicion should be kept for cases of episodic hypersomnolence for early diagnosis and management of KLS.
克莱恩-莱文综合征(KLS)是一种罕见的病症。其表现为亚急性起病的发作性嗜睡、认知功能减退、感知改变,偶尔伴有食欲亢进和性欲亢进,发作间期可完全恢复。5例患者表现为发作性嗜睡,符合KLS的诊断标准。大多数病例为女性(3/5),KLS在女性中更为罕见。首发年龄在10至25岁之间。认知功能障碍(5/5)、现实解体(4/5)、病毒前驱症状(3/5)、食欲亢进(3/5)和性欲亢进(2/5)是其他临床表现。非典型抑郁症的鉴别诊断是主要挑战,详细的病史采集有助于鉴别。使用兴奋剂(莫达非尼)和心境稳定剂(锂盐)治疗证明有效。对于发作性嗜睡的病例,应高度怀疑KLS,以便早期诊断和治疗。