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[A complete ventilation-perfusion mismatch following one-sided lung transplantation and postoperative hemothorax].

Eight days after single-lung transplantation for pulmonary hypertension, a patient presented with a hemothorax on the side of the transplanted lung that required acute thoracotomy. Pulmonary artery pressure had decreased from 78/32/58 mmHg prior to the transplant to 42/18/27 mmHg on the 2nd postoperative day. Therefore, a predominance of perfusion to the transplanted lung was expected. During induction of anesthesia, in spite of ventilation with pure oxygen the patient developed a hypoxic cardiac arrest (paO2 26 mmHg, 40% saturation measured by pulse oximetry) requiring external chest compression. Auscultation and chest movements suggested that the transplanted lung was not ventilated. Because blood flow went mainly to the transplanted lung, ventilation of the native lung was almost totally dead-space ventilation. To enable ventilation of the compressed transplanted lung, the patient was intubated using a single-lumen bronchial blocker tube to block the mainstem bronchus of the native lung. The transplanted lung could then be ventilated. Saturation increased and epinephrine re-established a stable circulation; 2500 ml blood were removed from the pleura without further complications. On the 7th postoperative day the patient was discharged from the intensive care unit without neurological deficits. A perfusion scan 28 days post-transplant revealed 89% of the perfusion going to the transplanted lung. Atelectasis of this lung resulted in a large intrapulmonary right-to-left shunt. Hypoxic pulmonary vasoconstriction could not ameliorate the shunt because of the high pulmonary vascular resistance of the native lung.(ABSTRACT TRUNCATED AT 250 WORDS)

Aged↗

[Hemothorax associated with congenital pulmonary arteriovenous fistula; report of a case].

A 20-year-old man was admitted to our hospital with a sudden onset of dyspnea, caused by right pleural effusion. The patient was in a state of shock. Thoracentesis was revealed hemothorax. Right thoracotomy revealed pulmonary arteriovenous fistula projecting into the intrapleural space from the right upper lobe. Partial resection was performed. His postoperative course was uneventful. Intrapleural rupture of pulmonary arteriovenous fistula was reported rarely; therefore we described here our case.

Adult↗

[Hemothorax following intraabdominal bleeding due to pedicle torsion of ovarian tumor via a small pore in the diaphragm: report of a case].

On February 25, 2004, 59-year-old woman visited a local clinic due to lower abdominal pain. On February 28, she was admitted to the clinic due to severe abdominal pain. Computed tomography (CT) showed a mass in the lower abdomen and plural effusion and athelectasis of the right lung. She had severe anemia (Hb 6.9 g/dl). On March 1, she was transferred to our hospital. Pleural fluid was revealed to be sanguineous by thoracentasis. She underwent thoracotomy on the day of admission. There was no source of bleeding in the pleural space. A small pore, 3 mm in diameter, was found in the tendinous portion of the diaphragm. An influx of bloody fluid from the abdomen via the pore caused hemothorax. Laparotomy was performed, followed by closure of the pore using direct suture. The origin of the abdominal bleeding was pedicle torsion of the right ovarian tumor. Seven months after surgery she was uneventful with no pleural effusion.

Abdominal Cavity↗

Spontaneous hemothorax caused by a ruptured intercostal artery aneurysm in von Recklinghausen's neurofibromatosis.

Aneurysms arising from an intercostal artery are very rare vascular malformations in von Recklinghausen's neurofibromatosis, which often have a silent clinical presentation and are difficult to diagnose before rupture. We report a case of von Recklinghausen's neurofibromatosis with massive hemothroax caused by spontaneous rupture of an intercostal artery aneurysm in a 29-year-old man. The diagnosis was eventually confirmed by percutaneous angiography and treated with endovascular embolization. During a 10-month follow-up period, the patient had a satisfactory recovery. This case illustrates that angiography and possible endovascular embolization should be the first strategy in managing hemothorax in patients with von Recklinghausen's disease.

Adult↗

Complete left-sided absence of the pericardium in association with ruptured type A aortic dissection complicated by severe left hemothorax.

We report an unusual clinical presentation of an acute type A aortic dissection as a left hemothorax in a patient with a congenital pericardial defect. Although the pericardial defect was diagnosed preoperatively, we could not exclude the possibility of a ruptured descending aorta until we discovered the site of the rupture during operation. The presence of a pericardial defect would at first appear to be a fatal disadvantage in such a situation as this, due to massive bleeding into the pleural space; but we believe that in our patient spontaneous drainage of blood into the pleural cavity prevented severe cardiac tamponade. The only reason for his deteriorating hemodynamic status was hypovolemia, which was corrected with volume replacement.

Aortic Dissection↗

Massive hemothorax in a beta-thalassemic patient due to spontaneous rupture of extramedullary hematopoietic masses: diagnosis and successful treatment.

Intrathoracic extramedullary hematopoiesis is an unusual but well-described entity. The condition is typically found in patients who have chronic hemolytic anemias, especially thalassemia. We report a case of a 38-year-old man with underlying beta thalassemia/hemoglobin E who developed intrathoracic extramedullary hematopoiesis. The hematopoietic masses spontaneously ruptured, resulting in massive hemothorax. The condition was confirmed by video-assisted thoracoscopy and successfully treated with surgery, hydroxyurea, and radiation.

Adult↗

Traumatic hemothorax resulting from rupture of mediastinal teratoma: a case report.

Ruptured cystic mature teratoma of anterior mediastinum is rare. This 45-year-old woman complained of sudden onset of chest pain and dyspnea after a traffic accident. Physical examination revealed decrease of breath sounds over the left chest. Chest X-ray showed pleural fluid accumulation of the left pleural cavity. Computed tomography scan of the chest revealed a heterogenous cystic mass lesion approximately 11.5 x 10 x 7 cm in size in the left anterior mediastinum and left pleural effusion. Under the impression of mediastinal tumor and traumatic hemothorax, she received excision of the mediastinal mass and evacuation of left pleural fluid through a left lateral thoracotomy. She recovered uneventfully after operation and was discharged on postoperative day 11.

Accidents, Traffic↗

Benign gestational trophoblastic disease metastatic to pleura: unusual cause of hemothorax.

A unique case of hemothorax caused by proven pleural involvement with benign gestational trophoblastic disease and anticoagulation is presented. The pulmonary manifestations of gestational trophoblastic disease are reviewed. It is stressed that these may be associated with histologically benign as well as frankly malignant disease, and that the clinician must be alert for them in managing all patients with known or suspected gestational trophoblastic disease.

Adolescent↗

Hemothorax in a patient with asthma.

Treatment of chronic illnesses such as asthma can often become routine. This is a case report that emphasizes the importance of a thorough history and physical examination for each exacerbation of asthma. An 11-year-old girl with a history of asthma presented to the emergency room with wheezing and dyspnea that was assumed to be an exacerbation of her chronic illness. After careful history taking and physical examination, a chest radiograph was recommended. The x-ray revealed a hemothorax and a new diagnosis was made, thoracic Ewing's sarcoma.

Asthma↗

Hemothorax--an unusual presentation of spinal fracture in ankylosing spondylitis.

Patients with ankylosing spondylitis are susceptible to spinal fractures. In many cases there is no history of associated trauma or only minor trauma. The instability of such fractures and complicating neurologic sequelae are well documented. We describe an unusual complication of ankylosing spondylitis, hemothorax secondary to spinal fracture, that to our knowledge has not been previously reported. Further, we reemphasize that the instability of such fractures may lead to significant paravertebral soft tissue and vascular injuries.

Fractures, Bone↗

Massive hemothorax and Groshong catheters.

Central vascular access with cannulation of either the subclavian or internal jugular vein is a common procedure in the hospital. Complications are rare, but may be severe. We report a case with a near fatal complication in the form of massive hemothorax 19 days after placement of a Groshong catheter.

Adult↗

[Successful surgical treatment of a patient with tension pneumopericardium and left hemothorax caused by multiple rib fractures].

A 62-year-old man underwent operation for tension pneumopericardium and left hemothorax caused by multiple rib fractures. He sustained other multiple injuries, such as acute subdural hematoma, compound fractures of the left leg. At left thoracotomy, massive hemorrhage from the left apical lung disrupted by the first and second fractured ribs was encountered and pericardium was seen to be bulging and tensely inflated. Incision of the pericardial sac resulted in expulsion of air with a subsequent fall in central venous pressure and heart rate. And after repair of the tear of the laceration of the left lung, the chest was closed with underwater seal drainages of the left pleural cavity. He was successfully weaned off the ventilator after 12 days. After extubation, repeated bronchoscopy was done, but the tracheobronchial injury was not able to be found out.

Hemothorax↗

Hemothorax associated with telangiectatic osteosarcoma in a dog.

Hemothorax in a dog was attributed to bleeding from an intrathoracic mass attached to the sixth through the tenth ribs. The mass contained numerous cavernous, blood-filled spaces as well as bands of osteoid and occasional foci of osseous tissue. The diagnosis was telangiectatic osteosarcoma. Telangiectatic osteosarcoma is an uncommon variant of osteosarcoma. Cavernous, blood-filled spaces and paucity of bone are important histologic features. Metastasis was described in one of the seven telangiectatic osteosarcomas reported in dogs, and none was found in this case.

Animals↗

[Hemothorax during subclavian catheterization. Risk factors not be neglected].

In the post operative course of a peritonitis, the need for a central venous catheter. A 800 ml hemothorax in the left pleura occurred. It could not be relieved with a chest-tube, and had to be evacuated through a thoracotomy. The risk factors to be considered in this case were sequellae of an inner third clavicle fracture and an arterial hypertension; although the patient was given a minimal dose of calcium heparinate.

Adult↗

Pneumothorax, hemothorax, and other abnormalities of the pleural space.

The clinical setting and treatment of various types of pneumothorax are detailed; chylothorax and hemothorax are also discussed. Tube thoracostomy, which can be performed with basic surgical skills if attention is paid to potential complications and optimal technique, is described.

Chylothorax↗

Neurofibromatosis and spontaneous hemothorax in pregnancy: two case reports.

Two cases of spontaneous hemothorax in pregnant women with neurofibromatosis are reported. Effects of pregnancy on the clinical course of neurofibromatosis are known to include worsening of cutaneous lesions, increased incidence of hypertension, and renal artery rupture. However, vessel wall rupture into the pleural cavity in areas of vascular neurofibromatosis is previously unreported. Contributing factors may include normal hemodynamic changes of the puerperium and pathological alterations of preexisting areas of neurofibromatosis. Because the incidence of vascular neurofibromatosis is not known and is difficult to diagnose, the serious morbidity and mortality encountered in this group place all pregnant patients with neurofibromatosis in a high-risk obstetric category.

Adult↗

Massive hemothorax in a child after removal of subclavian vein catheter.

A case is described where a near-fatal hemothorax developed in a child (age 13 months) right after the removal of the subclavian vein catheter. The catheter was introduced a week earlier and it had functioned without disorder. The possible mechanism of the complication is discussed. Even though this kind of complication is very rare, we recommend that the patients, especially children, must be carefully watched also after removal of the subclavian vein catheter to find a possibly life-threatening complication immediately.

Catheterization↗