Cases reported "Haemophilus Infections"

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1/9. Coexistent yellow nail syndrome and selective antibody deficiency.

    BACKGROUND: yellow nail syndrome (YNS) is a rare, often underdiagnosed condition of unknown origin. The clinical features of the syndrome include yellow nails, chronic sinusitis, bronchiectasis, pleural effusion, and lymphoedema. Despite the frequent occurrence of upper and lower respiratory tract infections in patients with YNS, comprehensive analysis of their humoral immunity has not been previously reported. OBJECTIVE: To present the case of a patient with YNS whose recurrent upper and lower respiratory tract infections may have been caused by an underlying selective antibody deficiency that manifests as impaired IgG antibody response to polysaccharide antigens. methods: The patient underwent cultures of purulent sputum for streptococcus pneumoniae and Haemophilus influenzae, bronchial washings for H. influenzae, and nail scrapings for fungi. Her serum levels of IgG, IgA, IgM, IgG subclasses, and serum titers of IgG antitetanus toxoid, anti-H. influenzae, and anti-S. pneumoniae antibodies were measured. RESULTS: Cultures of purulent sputum were positive on multiple occasions for S. pneumoniae and H. influenzae and bronchial washings were positive for H. influenzae. Nail scrapings were consistently negative for fungi. She had no reductions in serum levels of IgG, IgA, IgM, or IgG subclasses and had normal serum titers of IgG antitetanus toxoid antibodies. However, she demonstrated impaired IgG antibody responses following immunization with Pneumovax and an H. influenza B vaccine. CONCLUSIONS: This case report describes the first comprehensive analysis of humoral immune function in a patient with YNS. The finding of a selective antibody deficiency in our patient provides a potential explanation for the occurrence of respiratory infections in YNS. Accordingly, we recommend that functional antibody determinations and quantitative serum immunoglobulins be evaluated in patients diagnosed as having this unusual, enigmatic syndrome.
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2/9. Intrafamily spread of Haemophilus type b infections.

    meningitis and epiglottitis are the clinical manifestations of severe Haemophilus influenzae serotype b infection. Compared with meningitis, epiglottitis occurs in older children. When secondary cases occur within the family, the type of clinical manifestation produced by this serotype is generally similar in siblings. This report concerns the unusual occurrence of meningitis developing in older child and epiglottitis developing in the younger one. We discuss the possible explanations for this unusual pattern. We also survey the spread of H influenzae both within and outside the family unit and review the present status of histocompatibility antigens and Haemophilus disease.
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3/9. Secondary cases of invasive disease caused by spread of haemophilus influenzae type b.

    Three 6-year-old girls were admitted to hospital within a period of 9 days because of invasive disease caused by haemophilus influenzae type b (Hib). Two days after the index case contracted bacterial meningitis, her twin sister developed septicemia. Nine days after onset of illness in the index case, a day-care contact developed a febrile illness. The antibiograms of the bacterial strains isolated from cerebrospinal fluid or blood in the first two cases were identical; in the third case, blood cultures were negative but Hib antigen could be detected in serum and in urine. These cases illustrate the contagiousness of Hib disease. All household contacts of a case should be informed about the risk and their protection with rifampicin considered.
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4/9. Whipple's disease: a case with circulating immune complexes.

    A patient with Whipple's disease was studied for 56 wk from diagnosis, during which time he received continuous antibiotic therapy. Intramucosal bacillary bodies detected by electron microscopy disappeared within 12 wk and a threefold fall in antibody titer to Hemophilus influenza type B bacillus occurred during this period. Circulating immune complexes of IgG class were consistently detected during the first 28 wk of treatment but not subsequently. IgM class immune complexes were detected at a time when mucosal recovery had occurred and when IgG complexes were no longer detectable. A further rise of IgM immune complexes could be induced by enteric challenge with bovine serum albumin in our patient but not in control subjects. The detection of serum immune complexes in Whipple's disease may reflect the entry of foreign antigen through intestinal mucosa. These observations also support the possibility of an underlying defect of antigen exclusion in this disorder, which persists despite apparent mucosal recovery.
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5/9. cefamandole failure in ampicillin-resistant Haemophilus influenzae b pneumonia.

    A woman with rheumatoid arthritis and ampicillin-resistant haemophilus influenzae type b (Hib) pneumonia complicated by bacteremia and empyema is reported. Initial therapy with cefamandole failed to eliminate bacteria from the pleural space and did not substantially affect the clinical course. However, cultures became negative and fever resolved when therapy was changed to chloramphenicol. ampicillin-resistant Hib pneumonia in adults is an increasing problem and may be a difficult diagnosis to establish initially. counterimmunoelectrophoresis may be useful in adults with pneumonia. If Hib antigen is detected, or if H influenzae is suspected on the basis of Gram stains and cultures, chloramphenicol should be given until the isolate is shown to be sensitive to ampicillin.
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6/9. Outer membrane protein subtypes and investigation of recurrent haemophilus influenzae type b disease.

    Ten previously healthy patients, ages 3 to 26 months, developed recurrent episodes of deep-tissue haemophilus influenzae type b infections from 4 to 191 days (median = 28 days) after the last day of antibiotic therapy given for the first episode. None of the patients had a persistent focus of infection and eight were considered to have had adequate therapy for the initial episode. bacteremia, without evidence of relapse at the site of the original infection, was documented in eight of the ten recurrent episodes. The ampicillin susceptibilities of the HITB isolates changed between episodes in two of the patients. blood or CSF isolates from both episodes in seven patients were examined for biotypes and outer membrane protein subtypes. Concordance of both biotype and OMP subtype was present for all seven paired isolates, including the two pairs in which the HITB ampicillin sensitivities had changed. These data imply that some patients become reinfected with their original HITB isolates and that OMP and capsular antigens do not always elicit protective immunity, even after natural infection.
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7/9. Pediatric gonococcal infection: case report demonstrating diagnostic problems in remote populations.

    The inability of neisseria gonorrhoeae to survive prolonged transit times and hostile ambient temperatures has made its detection at referral laboratories by cultural methods untenable. In this situation, reliance upon antigen detection systems is attractive but when these tests are performed on vaginal specimens from children, false positive results are a significant concern. Some of the difficulties associated with the investigation of a gonococcal infection resulting from sexual abuse of a child in an isolated community are illustrated in this report.
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8/9. Bacterial endocarditis. Echocardiographic and clinical evaluation during therapy.

    In two patients with bacterial endocarditis and apparent vegetations, the echocardiographic findings included thickening but normal excursion of the mitral leaflet and abnormal shaggy echoes superimposed on the mitral leaflet echogram. Both patients had had endocarditis several weeks before the study was performed. In both patients the abnormal echoes disappeared after antibiotic therapy. Whether or not the echocardiographic findings are specific to bacterial endocarditis must be determined by further studies. One patient had evidence of "immune complex disease" with vasculitis, hypocomplementemia, and renal failure which persisted for weeks after disappearance of vegetations on the echocardiogram. This sequence was unexpected, as a continued source of antigen for this reaction was not apparent.
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9/9. Invasive haemophilus influenzae type b disease.

    Invasive bacterial disease due to Haemophilus influenzae is a cause of sudden death in children. It must be considered by medical examiners when a child dies with a fulminant course and nonspecific symptoms. Three fatal cases are presented in children 7 weeks to 15 months of age. Two had meningitis and petechiae or purpura. All three had bilateral adrenal hemorrhage and a rapidly fatal course. The potential for rapid and accurate diagnosis of H. influenzae infection is widely available due to latex agglutination technique against bacterial capsular wall antigens. diagnosis is critical because of its public-health implications. Up to 50% of cases may be acquired in day-care settings. Chemoprophylaxis is recommended for household and day care contacts. With the recent introduction of Haemophilus b conjugate vaccines for routine administration to infants beginning at 2 months of age, a change in the epidemiology of the disease is anticipated.
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