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神经母细胞瘤导致的后天性小儿间歇性霍纳综合征

Acquired Intermittent Pediatric Horner Syndrome due to Neuroblastoma.

作者信息

Cohen Liza M, Elliott Alexandra, Freitag Suzanne K

机构信息

Ophthalmic Plastic Surgery Service, Department of Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, Massachusetts.

出版信息

Ophthalmic Plast Reconstr Surg. 2018 Mar-Apr;34(2):e38-e41. doi: 10.1097/IOP.0000000000001001.

Abstract

A 3-month-old male developed intermittent left upper eyelid ptosis at the age of 1 month that was gradually increasing in frequency and duration. Examination revealed anisocoria and left upper and lower eyelid ptosis, consistent with a left Horner syndrome. Imaging showed a mass in the left superior posterior mediastinum, which was resected, and pathology was consistent with neuroblastoma. Eight months thereafter, the patient underwent left upper eyelid ptosis repair. Cases of infantile acquired Horner syndrome due to neuroblastoma are rare. To the authors' knowledge, there has only been one case described that presented with intermittent symptoms. The authors report the second case of intermittent acquired Horner syndrome due to neuroblastoma. This case demonstrates the importance of recognizing that Horner syndrome may present with subtle and intermittent symptoms. In a pediatric patient, one should maintain suspicion for neuroblastoma.

摘要

一名3个月大的男性在1个月大时出现间歇性左上睑下垂,其发作频率和持续时间逐渐增加。检查发现瞳孔不等大以及左上睑和下睑下垂,符合左侧霍纳综合征。影像学检查显示左上后纵隔有一肿块,予以切除,病理结果与神经母细胞瘤相符。8个月后,该患者接受了左上睑下垂修复术。因神经母细胞瘤导致的婴儿获得性霍纳综合征病例罕见。据作者所知,仅有一例报道表现为间歇性症状。作者报告了第二例因神经母细胞瘤导致的间歇性获得性霍纳综合征病例。该病例表明认识到霍纳综合征可能表现为细微和间歇性症状的重要性。对于儿科患者,应始终怀疑神经母细胞瘤。

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