Hemothorax resulting from hemorrhagic degeneration of giant uterine leiomyomata: A rare variant of pseudo-Meigs’ syndrome

IF 0.8 Q4 RESPIRATORY SYSTEM
Lawrence Huang , Tana Pradhan , Oleg Epelbaum
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引用次数: 0

Abstract

Though rare, hemothorax can occur without trauma, coagulopathy, or apparent vascular injury. Similar to the proposed mechanism of Meigs’ syndrome or hepatic hydrothorax, small diaphragmatic defects may allow peritoneal fluid to traverse the diaphragm into the pleural space. While typically this is associated with transudative pleural effusions, there have been case reports of hemoperitoneum crossing the diaphragm into the pleural space. Here, we present a case in which multiple giant leiomyomata with hemorrhagic necrosis led to hemoperitoneum that translocated across the diaphragm into the pleural space, causing a hemothorax.
巨大子宫平滑肌瘤出血性变性引起的血胸:一种罕见的伪梅格斯综合征变体
虽然罕见,但血胸可以在没有外伤、凝血功能障碍或明显血管损伤的情况下发生。与Meigs综合征或肝性胸水的机制类似,小的横膈膜缺陷可能使腹膜液穿过横膈膜进入胸膜间隙。虽然这通常与胸腔积液有关,但也有腹膜血穿过横膈膜进入胸腔间隙的病例报道。在此,我们报告一例伴有出血性坏死的多发性巨大平滑肌瘤导致腹膜出血,腹膜出血越过横膈膜进入胸膜间隙,引起血胸。
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来源期刊
Respiratory Medicine Case Reports
Respiratory Medicine Case Reports RESPIRATORY SYSTEM-
CiteScore
2.10
自引率
0.00%
发文量
213
审稿时长
87 days
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