Trimethoprim–sulfamethoxazole‐induced rhabdomyolysis in an allogeneic stem cell transplant patient

P.J. Kiel, N. Dickmeyer, J.E. Schwartz. Trimethoprim–sulfamethoxazole‐induced rhabdomyolysis in an allogeneic stem cell transplant patient.
Transpl Infect Dis 2010: 12: 451–454. All rights reserved Abstract: Rhabdomyolysis is a serious, potentially life‐threatening complication diagnosed when creatine phosphokinase levels exceed 1000 U/L. Although many drugs are associated with rhabdomyolysis, the previous reports of trimethoprim–sulfamethoxazole (TMP/SMX)‐induced rhabdomyolysis have involved patients with human immunodeficiency virus/acquired immunodeficiency syndrome. This is the first report, to our knowledge, of TMP/SMX‐induced rhabdomyolysis in an allogeneic stem cell transplant patient.     

Fumagillin‐induced aseptic meningoencephalitis in a kidney transplant recipient with microsporidiosis

Microsporidiosis is an opportunistic infection in organ transplant recipients and patients with other cellular immunodeficiency. Fumagillin is an effective treatment against Enterocytozoon bieneusi, one of the two main species causing the microsporidiosis involved in human diseases. We report the first case, to our knowledge, of a probable drug‐induced aseptic meningoencephalitis, after administration of fumagillin in a kidney transplant recipient with microsporidiosis.     

Dual infection with hepatitis A and E virus presenting with aseptic meningitis: a case report

We report the case of a young male who presented with features of aseptic meningitis and elevated serum liver enzymes, but no symptoms or signs suggestive of an acute hepatitis. Subsequently, he was diagnosed with dual infection with hepatitis A and E viruses, and recovered completely with symptomatic therapy. Isolated aseptic meningitis, unaccompanied by hepatitic features is an unusual presentation of a hepatotrophic viral infection, and is yet to be reported with hepatitis A and E virus co-infection.     

Nocardial meningitis: case reports and review

Twenty-eight episodes of nocardial central nervous system infection fulfilling criteria for meningitis were reviewed. In 21 cases Nocardia was cultured from cerebrospinal fluid (CSF). Associated predisposing conditions were present in 75% of cases. The typical presentation was subacute to chronic meningitis characterized by fever (68%), stiff neck (64%), and headache (55%). CSF studies revealed neutrophilic pleocytosis (83% of cases, greater than 500 white blood cells/mm3), hypoglycorrhachia (64%, less than 40 mg of glucose/dL), and elevated protein level (61%, greater than 100 mg/dL). In 43% of cases there was an associated brain abscess. Patients with brain abscess had more frequent and severe aberrations in mental status as well as higher initial white blood cell counts in CSF. Mortality was 52% for the 23 cases diagnosed antemortem and 57% overall. Compared with patients who died, survivors were younger, had lower initial CSF glucose levels, and were less likely to have brain abscess. Diagnosis was often delayed, and nocardial infection was rarely suspected before positive culture reports or autopsy findings became available.     

Anthrax meningitis: case report and review

We report a case of meningitis caused by Bacillus anthracis. Although this agent appears to be a rare pathogen, it should always be considered in the differential diagnosis of haemorrhagic meningitis cases owing to the high mortality rate associated with it.     

A rare case of cotrimoxazole-induced eosinophilic aseptic meningitis in an HIV-infected patient

A case of cotrimoxazole-induced meningoencephalitis in an HIV-infected patient without signs of AIDS is reported. The patient developed an apparently generalized seizure, of cotrimoxazole, 1 month after first taking a dose of this drug and a febrile coma after a second dose 3 weeks later. Lumbar puncture revealed eosinophilic aseptic meningitis. The patient quickly recovered without sequelae and was given antiretroviral therapy plus pentamidine aerosolized and pyrimethamine as prophylaxis for opportunistic infections. No other adverse effects were observed. The report describes the diagnosis of this case supported by a commentary, including a literature review.     

Ampulla cardiomyopathy induced by meningitis: two case reports

Two patients presented with ampulla cardiomyopathy induced by meningitis. A 71-year-old man with meningitis was admitted to our neurosurgery division. Emergent coronary angiography was performed, because of sudden blood pressure fall and ST elevation in the precordial leads. Left ventriculography and coronary angiography revealed apical ballooning without coronary stenosis. A 73-year-old woman with meningitis was admitted to another hospital. She felt chest pain. Electrocardiography showed ST elevation in the precordial leads. She was transferred to our division. Echocardiography revealed apical ballooning and hyperkinesis of the base. Creatine kinase level showed no elevation on admission or 8 hr later. Ampulla cardiomyopathy with cerebrovascular disease is common, but rare with meningitis, which needs intensive care because of the risk of respiratory arrest.     

Aseptic meningitis in relapsing polychondritis: a case report and literature review

Clinical Rheumatology - Aseptic meningitis is an extremely rare neurologic complication of relapsing polychondritis (RP). We reported a case of a 58-year-old Chinese female with intractable...     

Glucocorticoid‐induced hyperglycaemia in respiratory disease: a systematic review and meta‐analysis

The relative risk of glucocorticoid‐induced hyperglycaemia is poorly quantified. We undertook a meta‐analysis to estimate the association between glucocorticoid treatment and hyperglycaemia, overall and separately in individuals with and without diabetes and underlying respiratory disease. We searched electronic databases for clinical trials of adults randomized to either glucocorticoid treatment or placebo. Eight articles comprising 2121 participants were identified. We performed a random effects meta‐analysis to determine relative risks for the associations between glucocorticoid use and both hyperglycaemia and starting hypoglycaemic therapy. In all individuals, the relative risk of hyperglycaemia comparing glucocorticoid treatment with placebo was 1.72 [95% confidence interval (CI) 1.50‐2.04; p < .001]. The relative risks in individuals with and those without diabetes were 2.10 (95% CI 0.92‐5.02; p = .079) and 1.50 (95% CI 0.79‐2.86; p = .22), respectively. In all individuals, the relative risk of hyperglycaemia requiring initiation of hypoglycaemic therapy, comparing glucocorticoid treatment with placebo, was 1.73 (95% CI 1.40‐2.14; p < .001). In conclusion, glucocorticoid therapy increases the risk of hyperglycaemia in all individuals with underlying respiratory disease but not when diabetic status is analysed separately.     

Cryptococcal meningitis in an immunocompetent child: a case report and literature review

An immunocompetent 5 year-old girl presented with pyrexia of unknown origin associated with headache. Initial investigations showed leukocytosis and an increased erythrocyte sedimentation rate. A Widal-Weil Felix test, blood film for malarial parasites, mycoplasma IgM antibody, cultures from blood and urine, full blood picture, Mantoux test, and chest x-ray were all negative. A lumbar puncture was done as part of a work-up for pyrexia of unknown origin. Cryptococcus neoformans was seen on India ink examination and confirmed on culture. She was treated with 10 weeks of intravenous amphotericin B and 8 weeks of fluconazole. Further immunological tests did not reveal any defect in the cell-mediated immune system. C. neoformans meningitis may present with non-specific symptoms and should be considered in a work-up for pyrexia of unknown origin.