3 Occasionally aneurysms in this location can cause respiratory symptoms including dyspnea and hemoptysis.5 Symptoms caused by this condition are nonspecific and are usually interpreted by the physicians as the result of other underlying disease. Progressive http://www.selleckchem.com/products/Everolimus(RAD001).html dyspnea in our presented case was always treated as the sign of progressive heart failure due to the cardiomyopathy. Old trauma was not taken in the account. Only repeated CT scan suggested final diagnosis. We think that
in this case underlying pseudoaneurysm of brachiocephalic artery due to chest trauma progressed and enlarged quickly after bronchoscopic superficial biopsy and EBUS procedure. Careful radiological (especially CT scan) evaluation is mandatory before any diagnostic interventional procedure when chest tumor is suspected. The authors state no conflict of interest. “
“Methemoglobinemia, a disorder characterized by the presence of high methemoglobin levels in the blood, can occur in congenital and acquired forms. Methemoglobin is an oxidized form of hemoglobin, which has an increased affinity of oxygen and reduced ability to release oxygen to tissues. The oxygen–hemoglobin dissociation curve is
therefore shifted to the left. When methemoglobin concentration is elevated in red blood cells, tissue hypoxia may occur. This disorder may present with several symptoms such as cyanosis, dyspnea, headache. Because it is a rare cause of cyanosis and hypoxemia, the diagnosis of methemoglobinemia is oftenly delayed. Another reason of delayed diagnosis CH5424802 price is that unless methemoglobin levels above 40%, the disease often remains asymptomatic. The true diagnosis and treatment of methemoglobinemia reduces mortality. In this paper we present a congenital methemoglobinemia case who was treated with bronchodilator therapy for a period of nearly five
years because of misdiagnosis of asthma. 20-year-old male patient was admitted to our outpatient clinic of chest diseases with complaints of chest pain, exertional dyspnea and cyanosis. The patient stated that the complaints are present for 4–5 years and using inhaled bronchodilator cAMP therapy with a diagnosis of asthma. In physical examination, vital signs of the patient were normal. Cyanosis is present on the hands and lips, and SpO2 value was measured as 88–90% in room air. PaO2 was measured as 54 mmHg in arterial blood gas analysis. Upon this we performed chest radiography and pulmonary artery computerized tomography angiography with a prior diagnosis of pulmonary embolism (acute or chronic), but no pulmonary radiologic lesion was found. Subsequently, ecocardiography was performed for investigating the etiology of hypoxemia but any pathology was not found again. Although patients treated with nasal oxygen with a FiO2 value of 35%, SpO2% measurements were about 89–90%. When we received a more detailed history from patient it was learned that his big brother also had similar complaints and he had died for this reason.