Chylothorax-induced diaphragmatic herniation: a novel complication of Gorham-Stout syndrome.

IF 0.5 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2025-09-30 eCollection Date: 2025-09-01 DOI:10.1093/jscr/rjaf772
Quan Chen, Cuiyan Yang, Hui Chen, Chuanfeng Ke
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引用次数: 0

Abstract

A young male with Gorham-Stout syndrome (GSS), a rare lymphovascular disorder causing bone loss, presented with cough, difficulty breathing, and chylous pleural effusion infected with Staphylococcus aureus. Despite thoracic duct ligation, his chylothorax recurred. Imaging showed bone lesions in the sternum and ribs, along with thickened pleura. Electromyography revealed mild bilateral phrenic nerve motor conduction abnormalities. A year later, he developed a symptomatic left diaphragmatic hernia with partial bowel obstruction that required surgical repair. This case highlights the need for early diaphragm monitoring in GSS patients with chylothorax to prevent serious complications.

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乳糜胸引起的膈疝:Gorham-Stout综合征的新并发症。
一例年轻男性Gorham-Stout综合征(GSS),一种罕见的导致骨质流失的淋巴血管疾病,表现为咳嗽、呼吸困难和乳糜胸膜积液感染金黄色葡萄球菌。尽管进行了胸导管结扎术,他的乳糜胸还是复发了。影像学显示胸骨和肋骨病变,胸膜增厚。肌电图显示轻度双侧膈神经运动传导异常。一年后,他出现了有症状的左侧膈疝并伴有部分肠梗阻,需要手术修复。本病例强调了GSS合并乳糜胸患者早期膈肌监测的必要性,以防止严重的并发症。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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