Horner Syndrome Following Permcath Insertion in a Child with End-Stage Renal Disease: A Case Report.

IF 0.9 Q4 CLINICAL NEUROLOGY
Iranian Journal of Child Neurology Pub Date : 2025-01-01 Epub Date: 2025-03-11 DOI:10.22037/ijcn.V19i2.44855
Masoumeh Mohkam, Shiva Fatollahierad, Farzad Ahmadabadi, Mitra Khalili
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Abstract

Horner syndrome, characterized by the triad of unilateral ptosis, miosis, and anhidrosis, typically arises following a stroke, surgical interventions in the neck and chest, or trauma. Horner syndrome is rare in children. This study presents the case of a 9-year-old girl with End-Stage Renal Disease (ESRD) caused by renal hypodysplasia. After permcath insertion, she developed a severe headache and anisocoria, followed by ptosis and a progressively expanding neck hematoma. Physical examination and MRI of the neck revealed that Horner syndrome, caused by hematoma formation following permcath placement, was the diagnosis. Supportive interventions were implemented, leading to significant improvement in Horner syndrome over a six-month period. Complications from permcath insertion can be a cause of Horner syndrome.

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终末期肾脏疾病儿童插入永久导管后出现霍纳综合征1例报告。
霍纳综合征,以单侧上睑下垂、瞳孔缩小和无汗三联征为特征,通常在中风、颈部和胸部手术干预或创伤后出现。霍纳综合症在儿童中很少见。本研究报告一例9岁女童终末期肾脏疾病(ESRD)引起的肾脏发育不良。插入导管后,患者出现严重头痛和斜视,随后出现上睑下垂和逐渐扩大的颈部血肿。颈部体格检查和MRI显示,诊断为霍纳综合征,由永久性填埋后血肿形成引起。实施了支持性干预措施,在六个月的时间里,霍纳综合征得到了显著改善。从永久导管插入并发症可引起霍纳综合征。
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CiteScore
1.40
自引率
0.00%
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35
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