Management of Two Years Old Child with Russell-Silver Syndrome - A Case Report

Maryam Buenq, Mohamed Aziz Ullah Khan
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Abstract

Russell-Silver syndrome (RSS) is a rare genetic malformation characterized by the growth of a 2-year-old male child with RSS who underwent hip spica surgery under general anesthesia. The patient had a history of mild developmental delay, failure to gain weight, and frequent vomiting. Anesthetic implications of RSS, including airway management, glucose homeostasis, hypothermia, and pharmacological considerations, were considered during the patient's pre-operative assessment and intraoperative management. The patient was induced with propofol and fentanyl, and maintenance anesthesia was achieved with sevoflurane. The patient's airway was safely secured, and extubation was performed smoothly. The anesthetic management proceeded without complications, ensuring a successful outcome. This case report highlights the importance of considering the specific anesthetic implications of RSS in the perioperative management of patients with this rare genetic syndrome.
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2岁儿童Russell-Silver综合征1例的处理
Russell-Silver综合征(RSS)是一种罕见的遗传畸形,其特征是一名2岁的患有RSS的男孩在全身麻醉下接受了髋关节手术。患者有轻度发育迟缓、体重增加失败和频繁呕吐史。在患者术前评估和术中处理时,考虑了RSS的麻醉意义,包括气道管理、葡萄糖稳态、低温和药理学考虑。患者采用异丙酚和芬太尼诱导,七氟醚维持麻醉。患者气道安全,拔管顺利。麻醉处理过程无并发症,确保了成功的结果。本病例报告强调了在这种罕见遗传综合征患者的围手术期治疗中考虑RSS的特定麻醉含义的重要性。
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