Saurabh K. Singh, Deepak K. Pandey, Zuber Ahmad, Rakesh Bhargava
{"title":"New opacity","authors":"Saurabh K. Singh, Deepak K. Pandey, Zuber Ahmad, Rakesh Bhargava","doi":"10.1016/j.rmedc.2009.05.005","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.05.005","url":null,"abstract":"<div><p>Appearance of new opacity on the X-ray may simulate a disease and lead to the battery of test to confirm the disease. We are reporting case report when the patient with pleural effusion presented with the new opacity on follow up chest X-ray.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 76-77"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.05.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158522","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Primary Hodgkin's disease of the thymus","authors":"Ketata Wajdi, Msaad Sameh, Fouzi Salma, Abid Tarek, Ayadi Hajer, Ayoub Abdelkader","doi":"10.1016/j.rmedc.2009.02.006","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.02.006","url":null,"abstract":"<div><p>The thymus is a lymphoid organ located in the antero-superior mediastinum and composed of heterogeneous admixture of lymphoid and epithelial elements. Thymic tumors are dominated by thymoma; lymhomas are uncommon involving the gland secondary to adenopathies. Primary thymic lymphomas are exceptional.</p><p>We report a 25-year-old man referred to us because of chest pain and irritating cough since 2 months. Physical examination was normal and no lymph nodes were palpable. Chest radiography showed an anterior mediastinal mass. Computed tomography (CT) examination of the chest revealed a homogeneous tissular mass occupying the anterior mediastinum in its upper and medium stage, extending to the infundibulum without lymph node enlargement. Thymectomy and wedge were performed via a median sternotomy. Pathologic diagnosis was nodular sclerosis Hodgkin's disease of the thymus. The patient received 6 cycles of ABVD (Adriamycin [doxorubicin], bleomycin, vinblastin and dacarbazine) and mediastinal radiotherapy. Currently, tow years after diagnosis, he is well and free of disease.</p><p>Primary thymic Hodgkin's lymphoma is a rare entity which should be included in the differential diagnosis of anterior mediastinal mass especially in young patients.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 1","pages":"Pages 15-17"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.02.006","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136554836","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kohei Fujita, Young Hak Kim, Mitsuru Yoshino, Masataka Ichikawa, Tadashi Mio, Michiaki Mishima
{"title":"Acute Budd–Chiari syndrome caused by tumor thrombus of the inferior vena cava secondary to non-small cell lung cancer","authors":"Kohei Fujita, Young Hak Kim, Mitsuru Yoshino, Masataka Ichikawa, Tadashi Mio, Michiaki Mishima","doi":"10.1016/j.rmedc.2009.02.003","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.02.003","url":null,"abstract":"<div><p>Budd–Chiari syndrome secondary to lung cancer is very rare. The clinical features of this disease have not been well described, as only a few cases have been reported in the past 3 decades. We analyzed 5 such cases, including the present case, and have identified certain features of lung cancer that may play a role in this syndrome. All cases had cancers originating in the right lung, and 4 cases were patients with non-small cell lung cancers. Because of the rapid progression of liver failure, the prognosis for this syndrome is very poor, and the effects of chemotherapy and/or radiotherapy are limited. Recently, however, new treatments, such as stent placement therapy, have been shown to relieve pain and prolong life. We describe a rare case of acute Budd–Chiari syndrome caused by tumor thrombus of the inferior vena cava secondary to lung cancer. In addition, we discuss similar cases reported in the past 3 decades and the effectiveness of stent placement therapy.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 1","pages":"Pages 26-28"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.02.003","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"136554839","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Pleomorphic carcinoma of the lung: A case report with immunohistochemical studies","authors":"Tadashi Terada","doi":"10.1016/j.rmedc.2009.10.001","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.10.001","url":null,"abstract":"<div><p>Because incidence and immunohistochemical features of pulmonary pleomorphic carcinoma (PC) are unclear, the author retrospectively surveyed and re-examined the archival 718 lung malignancy samples in our laboratory. As the results, one case of pulmonary PC was found; thus the incidence of pulmonary PC was 0.14% of all lung malignancies. A 67-year-old woman with asthma was found to have a rapidly growing tumor in the peripheral lower lobe of right lung at a private clinic, and was referred to our hospital. She was a non-smoker. Imaging modalities showed a cystic tumor, and clinical diagnosis was bronchogenic cyst. Right lower lobectomy was performed. The patient is now alive without tumors six years after the operation. Grossly, the tumor was well-defined white tumor with necrosis. The tumor measured 5<!--> <!-->×<!--> <!-->4<!--> <!-->×<!--> <!-->5<!--> <!-->cm. Histologically, the tumor was pulmonary PC consisting of malignant spindle and giant cells with focal tubular formations. Necrotic foci and numerous mitotic figures were present. Immunohistochemically, tumor cells were positive for pancytokeratin, high molecular weight cytokeratin (CK), CK5/6, CK7, CK14, CK18, CK19, epithelial membrane antigen, vimentin, p53 protein, surfactant apoprotein A, neuron-specific enolase, lysozyme, Ki-67 (60%), and CD68. Tumor cells were negative for CK20, thyroid transcriptional factor-1, CEA, S100 protein, desmin, α-smooth muscle actin, melanosome, CD34, p63, chromogranin, synaptophysin, CD56, KIT, and platelet-derived growth factor-α. It appeared that the present pulmonary PC is associated with adenocarcinoma or derived from sarcomatous transformation of adenocarcinoma.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 4","pages":"Pages 252-256"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.10.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137088203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Management of isoniazid-resistant pulmonary tuberculosis in patient with non-functioning bowel on the intensive care unit","authors":"Katherine M. Coyne, Anton L. Pozniak","doi":"10.1016/j.rmedc.2009.05.002","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.05.002","url":null,"abstract":"<div><p>A young Turkish woman presented with abdominal sepsis. Terminal ileal Crohn's disease was diagnosed on histology. She was treated with intravenous steroids and bowel resection but required multiple laparotomies for recurrent peritonitis. Isoniazid-resistant <em>Mycobacterium tuberculosis</em> was cultured from sputum. Treatment of tuberculosis was complicated by a long post-operative period of non-functioning bowel, which necessitated intravenous agents.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 71-72"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.05.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A case of pulmonary melioidosis","authors":"J. Lie , S. Maxwell , C. Keeling-Roberts , D. Dev","doi":"10.1016/j.rmedc.2009.04.002","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.04.002","url":null,"abstract":"<div><p>Melioidosis is a rare infectious disease that is very prevalent in certain areas of the world, namely Thailand and certain parts of Northern Australia. There are only 29 cases being reported in the UK since 1988. With air transport industry getting more and more readily available and affordable, it is important to recognise this disease especially those who have recently travelled to those endemic regions. We report a case of a man who presented with pulmonary melioidosis after recent travel to Thailand.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 109-110"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.04.002","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158484","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mohammad Shameem , Syed M. Danish Qaseem , M. Azfar Siddiqui , Naveed Nazir Shah , Asrar Ahmad
{"title":"Mature mediastinal teratoma in adult","authors":"Mohammad Shameem , Syed M. Danish Qaseem , M. Azfar Siddiqui , Naveed Nazir Shah , Asrar Ahmad","doi":"10.1016/j.rmedc.2009.02.009","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.02.009","url":null,"abstract":"<div><p>A 21-year-old male, presented with dull aching chest pain, shortness of breath. CECT thorax reveals lobulated mediastinal mass containing soft tissue predominantly in superior and anterior mediastinum with a few foci of calcification seen along septae. CT guided FNAC was suggestive of teratoma. The patient underwent surgical resection.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 116-117"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.02.009","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Recent advances in the diagnosis and treatment of multidrug-resistant tuberculosis","authors":"Suhail Ahmad, Eiman Mokaddas","doi":"10.1016/j.rmedc.2010.08.001","DOIUrl":"https://doi.org/10.1016/j.rmedc.2010.08.001","url":null,"abstract":"<div><p>Tuberculosis (TB) is a major infectious disease killing nearly two million people, mostly in developing countries, every year. The increasing incidence of resistance of <em>Mycobacterium tuberculosis</em> strains to the most-effective (first-line) anti-TB drugs is a major factor contributing to the current TB epidemic. Drug-resistant strains have evolved mainly due to incomplete or improper treatment of TB patients. Resistance of <em>M. tuberculosis</em> to anti-TB drugs is caused by chromosomal mutations in genes encoding drug targets. Multidrug-resistant (resistant at least to rifampin and isoniazid) strains of <em>M. tuberculosis</em> (MDR-TB) evolve due to sequential accumulation of mutations in target genes. Emergence and spreading of MDR-TB strains is hampering efforts for the control and management of TB. The MDR-TB is also threatening World Health Organization’s target of tuberculosis elimination by 2050. Proper management of MDR-TB relies on early recognition of such patients. Several diagnostic methods, both phenotypic and molecular, have been developed recently for rapid identification of MDR-TB strains from suspected patients and some are also suitable for resource-poor countries. Once identified, successful treatment of MDR-TB requires therapy with several effective drugs some of which are highly toxic, less efficacious and expensive. Minimum treatment duration of 18–24 months is also long, making it difficult for health care providers to ensure adherence to treatment. Successful treatment has been achieved by supervised therapy with appropriate drugs at institutions equipped with facilities for culture, drug susceptibility testing of MDR-TB strains to second-line drugs and regular monitoring of patients for adverse drug reactions and bacteriological and clinical improvement.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 2","pages":"Pages 51-61"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2010.08.001","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137158519","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kurugundla Navatha, Wei Li , Chukuma Okadigwe , Tom Russi , Rocco Franco
{"title":"Tularemia presenting as a unilateral pleural effusion in a metropolitan city","authors":"Kurugundla Navatha, Wei Li , Chukuma Okadigwe , Tom Russi , Rocco Franco","doi":"10.1016/j.rmedc.2009.07.005","DOIUrl":"https://doi.org/10.1016/j.rmedc.2009.07.005","url":null,"abstract":"<div><p>We report a young patient who went on a camping trip to a local park in a metropolitan area complaining of chest pain. On further investigations, he was found to have left sided pleural effusion. Thoracentesis revealed alkaline PH and the fluid was an exudate. The culture grew <em>Francisella tularensis</em>. The patient was treated with streptomycin with marked clinical improvement.</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 3","pages":"Pages 195-197"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.07.005","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137350420","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}