ABSTRACT
We report 2 cases of Myocardial Bridge (MB). MB, even though a very frequent anomaly (found out in 85% of autopsies), often is asymptomatic. It is hard to diagnose in patients affected by coronary artery disease, seldomly found out on selective coronary angiograms (in 16-20% of chest pain cases). MB can be considered as one of the causes of coronary artery disease.
Subject(s)
Coronary Artery Disease/etiology , Coronary Vessel Anomalies/complications , Aged , Coronary Angiography , Coronary Vessel Anomalies/diagnosis , Coronary Vessel Anomalies/physiopathology , Echocardiography/methods , Electrocardiography , Humans , MaleABSTRACT
Clinical manifestations of pulmonary tuberculosis (TB) may depend on a complex interaction between the host and the pathogen. Clinical outcomes of pulmonary tuberculosis are variable, ranging from asymptomatic lifelong infection to parenchymal lung destruction, resulting in cavitary lesions. To investigate the hypothesis that local cellular immune response may affect presentation and outcome in tuberculosis, we performed bronchoalveolar lavage (BAL) in lung segments affected by cavitary and non-cavitary tuberculosis. We then correlated the type of cellular response at the level of the involved lung segments with clinical evolution in terms of cavity formation. We found alveolar lymphocytosis in patients with both cavitary and non-cavitary pulmonary tuberculosis, with increased CD4+ lymphocytes in patients with non-cavitary pulmonary tuberculosis. A predominant Th1 immune response has been observed in non-cavitary patients, while cavitary involved segments exhibit the presence of Th2 lymphocyte subsets. These data, while confirming the importance of Th1-type CD4+ cells and IFN-gamma in effective cellular immunity in active pulmonary tuberculosis, also suggest that the presence of Th2 lymphocytes may contribute to tissue necrosis phenomena associated with cavitary evolution of pulmonary tuberculosis. Our observations indicate the importance of the type of local immune response at the site of disease in the development of different clinical characteristics and outcome in pulmonary tuberculosis.
Subject(s)
Lung/immunology , T-Lymphocytes/immunology , Tuberculosis, Pulmonary/immunology , Adult , Aged , Bronchoalveolar Lavage Fluid/immunology , CD4 Lymphocyte Count , Case-Control Studies , Disease Progression , Female , Humans , Immunophenotyping , Lung/pathology , Lymphocyte Count , Male , Middle Aged , Th1 Cells/pathology , Th2 Cells/pathology , Tuberculosis, Pulmonary/pathologyABSTRACT
Primary cutaneous plasmacytomas of the chest wall are very rare. In this report we describe a case of a 70-years old man, affected by chronic obstructive pulmonary disease and renal failure. He was admitted because of a painful tumor on the right lateral chest wall: a transcutaneous fine needle aspiration and excisional biopsy revealed as a metastasis from lung cancer without clinical and or radiological evidence of pulmonary tumors and or other neoplasms. Because of failure of chemotherapy, the patient had undergone to bone marrow biopsy that it revealed medullary plasmacytosis < 5% plasma cells with a beta 2 microglobulin elevated. An other following excisional biopsy of a chest wall with immunocytochemistry revealed to be a cutaneous plasmacytomas. The patient was treated with local irradiation for a total dose of 40 cGy and systemic chemotherapy, stopped because of death by myocardial infarction. Cutaneous plasmacytomas appear to be more aggressive than non cutaneous extramedullary plasmacytomas; they should be separately categorized from them in future studies.
