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Query: UMLS:C0010200 (cough)
 23,843 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In the absence of recognized pneumonitis, psittacosis is unlikely to be considered as a cause of infection in patients with febrile illnesses. To identify findings useful in the diagnosis of psittacosis, the clinical and roentgenographic characteristics of 46 cases that occurred in two outbreaks among workers in turkey processing plants were reviewed. Headache (96% of patients), chills (93% of patients), and fever (89% of patients) were the most common symptoms; a nonproductive cough occurred in 65% of patients. Rales or rhonchi were detected in only six (18%) of 33 patients examined, but 21 (72%) of 29 patients receiving a chest film had roentgenographic evidence of pneumonia. We conclude that few diagnostically useful symptoms or signs occur in patients with psittacosis but that roentgenographically confirmed pneumonitis may occur commonly in patients with little clinical evidence of pneumonitis. A history of exposure to birds, in an individual with a flu-like illness, appears to be the single best clue to the diagnosis of psittacosis.
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PMID:Psittacosis. A diagnostic challenge. 649 78

22 patients with primary Sjogren's syndrome were prospectively studied for respiratory system involvement with clinical, roentgenological and functional parameters. 12 patients (55%) had respiratory manifestations. In 10/12 (83%), respiratory symptoms occurred before or concomitantly with the classical symptoms of Sjogren's syndrome. There were two distinct forms of respiratory involvement: xerotrachea, manifested by dry cough without other symptoms and negative roentgenological and functional evaluation and diffuse interstitial lung disease manifested by dyspnea with or without dry cough with bibasilar rales, compatible chest roentgenogram, restrictive pattern in spirometry and/or hypoxemia. Xerotrachea was more common in patients with glandular form of Sjogren's syndrome (3/10) and diffuse interstitial lung disease in patients with extraglandular form (6/12). None of the 22 patients had pleurisy or other forms of respiratory involvement. Antibodies to Ro (SSA) and La (SSB) antigens were more common in patients with the extraglandular form of the syndrome but did not correlate with diffuse interstitial lung disease.
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PMID:Xerotrachea and interstitial lung disease in primary Sjogren's syndrome. 649 25

We have examined 221 cases of mycoplasmal pneumonia in adults during the past 17 years. During this time epidemic waves occurred every three to four years. The incidence of disease was highest in patients 20 to 30 years of age. The most common clinical features were cough, fever, sputum, and rales. The most characteristic feature was a persistent cough which lasted about three to four weeks. Roentgenographic examinations showed a variety of patterns, but the most consistent feature was a feathery shadow, appearing in the lower field of either or both of the lungs. Lung function tests showed peripheral airway impairment. Although roentgenographic examination provided useful information, it could not be used as a pathognomic feature of mycoplasmal pneumonia. Tetracyclines were most effective for eliminating clinical symptoms, whereas the macrolides provided the best response based on roentgenographic evaluations.
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PMID:Clinical features of mycoplasmal pneumonia in adults. 667 46

From summer to mid-autumn for four consecutive years (1974 to 1977), a 50-year-old woman barber experienced cough and exertional dyspnea with sputum production. Rales were audible at the posterior lung bases bilaterally. Her chest x-ray film showed diffuse nodular shadows, and pulmonary function studies revealed markedly decreased DCO. Open chest lung biopsy was performed and granulomatous lesions with multinucleated giant cells without central necrosis were observed. Having experienced multiple episodes for four years, she ceased to show symptoms after demolishing and reorganizing her house. This case is thought to represent the typical summer-type hypersensitivity pneumonitis, which we have subsequently found to be the most prevalent form of hypersensitivity pneumonitis in Japan.
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PMID:Clinical episodes of granulomatous pneumonitis. Repetition during four consecutive summers. 669 11

Hypersensitivity pneumonitis (extrinsic allergic alveolitis) represents a spectrum of granulomatous, interstitial, and alveolar-filling lung disorders of which farmer's lung is a classic example. A major source of offending antigens in these diseases are thermophilic actinomycetes growing in moldy vegetable matter especially Micropolyspora faeni, and members of the Thermoactinomyces genus. Acutely, hypersensitivity pneumonitis presents as cough, dyspnea and fever, with crepitant rales, leucocytosis, diffuse interstitial and alveolar pulmonary infiltrates and a restrictive-type pulmonary functional deficit. Symptoms usually begin 4 to 6 hr after exposure to large quantities of causative organic dust. Chronically, these diseases may present with the gradual onset of cough, dyspnea on exertion, fatigue, anorexia, and weight loss which may progress to pulmonary fibrosis or severe pulmonary insufficiency. While early ideas on the pathogenesis of hypersensitivity pneumonitis support the role of Type III immune complex hypersensitivity, more recent evidence attests to the important and integral role of Type IV or delayed-type hypersensitivity. It is the purpose of this review, therefore, to describe those immune mechanisms relevant to the pathogenesis of hypersensitivity pneumonitis and stress the importance of "local" pulmonary immune responsiveness.
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PMID:Immunology of hypersensitivity pneumonitis. 676 Oct 66

Sixteen patients with chronic bronchitis were treated in a single-blind crossover study during two separate acute exacerbations caused by bacterial infections. During one of the episodes a regimen consisting of two 800-mg doses of bacampicillin per day was given; therapy for the other episode was four 500-mg doses of ampicillin per day. Each drug was given for 14 days. Patients were observed once before therapy was started, twice a week during therapy, and weekly after therapy; the investigator did not know which drug the patients were receiving. Graded clinical observations included frequency and severity of cough, wheezing, rales, rhonchi, breath sounds, and prolongation of expiration. Objective sputum measurements included daily volume, qualitative and quantitative cytology, and quantitative bacterial counts. Paired t-test analyses revealed that before therapy was begun the group receiving bacampicillin was sicker. Both agents effectively decreased inflammation and counts of bacterial flora. Clinical symptoms cleared 11 days after institution of therapy with either drug, but patients tended to favor bacampicillin in overall clinical effects. Adverse effects were similar with both agents, but bacampicillin was associated with fewer upper and more lower gastrointestinal symptoms.
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PMID:Comparison of bacampicillin twice daily and ampicillin four times daily in treatment of acute exacerbations of chronic bronchitis. 701 95

An outbreak of respiratory disease occurred in a herd of 34 calves and 5 cows in a barn. The disease which affected 24 calves and 1 cow, was characterized by coughing, fever, anorexia, nasal discharge and pulmonary rales. Two calves died 5 days after the disease outbreak and were necropsied. Bronchitis, bronchiolitis and alveolitis were among the lesions observed in these calves. Bovine respiratory syncytial virus was detected, in lung sections of the dead calves and also in nasal washings of some of the calves and one cow, by the direct fluorescent antibody technique and/or cell culture method. Seroconversion to the virus was detected in most animals tested.
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PMID:A natural outbreak of bovine respiratory disease caused by bovine respiratory syncytial virus. 710 64

A retrospective study of 35 patients with Rocky Mountain spotted fever was undertaken to determine the frequency of respiratory symptoms, as well as to analyze the types of pulmonary problems encountered to hospital patients. Cough, present in only 33% of patients, led to an incorrect initial diagnosis and delay in therapy in eight individuals. Lower respiratory tract involvement (rales, abnormal chest roentgenograms, and abnormal gas exchange) was present in 42% of patients at some point during the illness. The conditions of nine patients deteriorated during the first week of hospitalization. Pulmonary edema (probably noncardiogenic) was the usual explanation for worsening gas exchange. Bacterial pneumonia and hemorrhage were detected in only two patients.
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PMID:Lower respiratory tract involvement in Rocky Mountain spotted fever. 735 17

Interstitial pneumonitis in children is a rare and poorly understood disease. Controversy exists as to whether the varoius histologic changes encountered represent different disease or a spectrum of the same disease. Fourteen biopsy-confirmed cases of desquamative interstitial pneumonitis in children were seen at the Mayo Clinic between 1953 and 1975. A search of the literature revealed 14 additional cases but no series of exclusively desquamative interstitial pneumonitis. The most frequent symptoms were retardation of growth and dyspnea, often accompanied by cough. Tachypnea was the most common finding on examination; rales, cyanosis, and clubbing were variably present. The chest roentgenogram was distinctly abnormal in all cases; it usually revealed a combined interstitial and alveolar pattern extending bilaterally from the hilus to the base. Results of laboratory studies were nonspecific for desquamative interstitial pneumonitis. All 28 patients in this review were treated with corticosteroids; 17 (61 percent) survived. Desquamative interstitial pneumonitis was found in association with a variety of other major illnesses. The cause remains unknown.
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PMID:Desquamative interstitial pneumonitis in children. 735 10

A 14-year-old girl with infectious mononucleosis and secondary immunosuppression had severe dyspnea and cough, spiking fever, rales, and diffuse bilateral pulmonary infiltrates. The pulmonary disease progressed rapidly, necessitating empiric trials of antimicrobial agents. Mycoplasma pneumoniae was isolated from a lung biopsy specimen, transtracheal aspirate, and expectorated sputum, but the relatively long period required to isolate the organism delayed the microbiologic diagnosis. Serologic study of acute and convalescent serum samples confirmed the M pneumoniae infection. Clinical improvement was gradual, and the immunosuppression was transient. The patient's illness appeared to represent microbial synergism, with severe M pneumoniae infection complicating transient immunosuppression induced by infectious mononucleosis.
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PMID:Infectious mononucleosis complicated by severe Mycoplasma pneumoniae infection. 740 10


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