Ishibashi Naoya, Yabe Ryuga, Ueda Kazunori, Nonomura Ryo, Oshima Yutaka, Sasaki Takanobu, Sugawara Takafumi, Niikawa Hiromichi
Thoracic Surgery, Tohoku Medical and Pharmaceutical University, Sendai, JPN.
Thoracic Surgery, Tohoku Medical And Pharmaceutical University, Sendai, JPN.
Cureus. 2025 Aug 8;17(8):e89615. doi: 10.7759/cureus.89615. eCollection 2025 Aug.
Neurofibromatosis type 1 (NF-1) is an autosomal dominant disorder associated with vascular abnormalities, including spontaneous hemothorax and arterial aneurysms. We present a rare case of spontaneous hemothorax in which an apparently hemostatic sub-pleural hematoma began to bleed again after the patient was repositioned. A 47-year-old man with NF-1 presented with the sudden onset of left-sided chest pain. Contrast-enhanced chest computed tomography revealed a massive left-sided hemothorax with a tortuous intercostal artery and an adjacent hematoma. The patient underwent emergency video-assisted thoracoscopic surgery (VATS), which revealed extensive intrathoracic clots and a subpleural hematoma near the aortic arch. Although no active bleeding was observed intraoperatively, hemostatic agents were applied to the suspected site. However, massive rebleeding occurred following patient repositioning, prompting an urgent re-thoracotomy. Active bleeding from the intercostal artery was identified and successfully controlled. The patient recovered without recurrence of hemothorax. Spontaneous hemothorax in patients with NF-1 warrants early recognition and surgical intervention. Vascular reconstruction is often challenging due to arterial fragility, underscoring the importance of careful intraoperative hemostasis and treatment selection. Furthermore, surgeons should be aware that temporary hemostasis may be achieved due to tamponade by a subpleural hematoma, potentially masking an underlying vascular injury. Careful intraoperative assessment and readiness for reintervention are essential in managing such cases.
1型神经纤维瘤病(NF-1)是一种常染色体显性疾病,与血管异常有关,包括自发性血胸和动脉瘤。我们报告一例罕见的自发性血胸病例,该病例中,一个看似已止血的胸膜下血肿在患者重新定位后再次出血。一名47岁患有NF-1的男性因突发左侧胸痛就诊。胸部增强计算机断层扫描显示左侧大量血胸,伴有迂曲的肋间动脉和相邻的血肿。患者接受了急诊电视辅助胸腔镜手术(VATS),术中发现胸腔内有广泛的血凝块,主动脉弓附近有一个胸膜下血肿。尽管术中未观察到活动性出血,但仍在可疑部位应用了止血剂。然而,患者重新定位后发生了大量再次出血,促使紧急再次开胸手术。术中确定肋间动脉有活动性出血并成功控制。患者康复,血胸未复发。NF-1患者的自发性血胸需要早期识别和手术干预。由于动脉脆弱,血管重建往往具有挑战性,这凸显了术中仔细止血和选择治疗方法的重要性。此外,外科医生应意识到,胸膜下血肿可能会起到压迫作用,从而实现暂时止血,这可能会掩盖潜在的血管损伤。术中仔细评估并做好再次干预的准备对于处理此类病例至关重要。