Sonokawa Takumi, Matsui Takuma, Takegahara Kyoshiro, Inoue Tatsuya, Kashiwada Takeru, Terasaki Yasuhiro, Usuda Jitsuo
Department of Thoracic Surgery, Nippon Medical School Hospital, 1-1-5 Sendagi, Bunkyo-ku, Tokyo, 113-8603, Japan.
Department of Pulmonary Medicine and Oncology, Graduate School of Medicine, Nippon Medical School, Tokyo, 113-8603, Japan.
Surg Case Rep. 2019 Feb 18;5(1):27. doi: 10.1186/s40792-019-0589-6.
Pulmonary hematoma is most often caused by thoracic trauma. However, rare cases of pulmonary hematoma without any obvious cause are sometimes reported, when the condition is referred to as spontaneous or idiopathic pulmonary hematoma. Herein, we report a very rare case-to the best of our knowledge, this is the first case of pulmonary hematoma associated with diffuse pulmonary ossification requiring emergency treatment reported in the English literature.
Our patient was a 44-year-old man with a history of IgA nephropathy and had no history of trauma or anticoagulant use. He presented with the chief complaint of bloody sputum and was referred to our hospital for detailed examination. Chest computed tomography showed a right pleural effusion and a large round mass in the right lower lobe. We performed chest tube drainage of the right thorax and confirmed bloody pleural effusion. Although bronchial artery embolization was performed, the patient's anemia worsened, and we performed right lower lobectomy. Histopathological examination of the resected specimen showed a hematoma with diffuse pulmonary ossification, although the relationship between the two was unclear. There was no evidence of malignancy or angiitis. Therefore, we made the diagnosis of spontaneous pulmonary hematoma in this case. The postoperative course was uneventful. The patient is currently under observation as an outpatient, and a recent chest X-ray showed no evidence of recurrence.
We report a case of spontaneous pulmonary hematoma with diffuse pulmonary ossification. Although the relationship between the two remains unclear, considering the possibility of appearance of new lesions/recurrence, we believe that careful follow-up is necessary for this patient.
肺血肿最常见的病因是胸部创伤。然而,有时会报告一些无明显病因的罕见肺血肿病例,这种情况被称为自发性或特发性肺血肿。在此,我们报告一例非常罕见的病例——据我们所知,这是英文文献中报道的首例与弥漫性肺骨化相关且需要紧急治疗的肺血肿病例。
我们的患者是一名44岁男性,有IgA肾病病史,无创伤或抗凝药物使用史。他以咯血为主诉就诊,被转诊至我院进行详细检查。胸部计算机断层扫描显示右侧胸腔积液和右下叶有一个大的圆形肿块。我们对右侧胸腔进行了胸腔闭式引流,并证实为血性胸腔积液。尽管进行了支气管动脉栓塞术,但患者贫血加重,于是我们进行了右下叶切除术。切除标本的组织病理学检查显示为伴有弥漫性肺骨化的血肿,尽管两者之间的关系尚不清楚。没有恶性肿瘤或血管炎的证据。因此,我们在该病例中诊断为自发性肺血肿。术后过程顺利。患者目前作为门诊患者接受观察,近期胸部X线检查未显示复发迹象。
我们报告了一例伴有弥漫性肺骨化的自发性肺血肿病例。尽管两者之间的关系尚不清楚,但考虑到可能出现新病变/复发的可能性,我们认为对该患者进行仔细的随访是必要的。