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2.
Scand J Infect Dis ; 39(5): 472-5, 2007.
Article in English | MEDLINE | ID: mdl-17464876

ABSTRACT

A case of leptospirosis complicated with meningo-myelo-encephalo-polyneuritis and nephrotic syndrome is presented. Anti-ganglioside antibodies were detected for the first time in a patient with neurological complications of leptospirosis. Possible pathogenic mechanisms and treatment options of these rare manifestations are discussed.


Subject(s)
Gangliosides/immunology , Leptospira/pathogenicity , Leptospirosis/complications , Meningoencephalitis/immunology , Neuritis/immunology , Aged , Antibodies/blood , Humans , Male , Meningoencephalitis/microbiology , Nephrotic Syndrome/microbiology , Neuritis/microbiology
3.
Eur J Gastroenterol Hepatol ; 18(5): 557-9, 2006 May.
Article in English | MEDLINE | ID: mdl-16607156

ABSTRACT

McKittrick-Wheelock syndrome is a rare disorder caused by fluid and electrolyte hypersecretion from a rectal tumour. The most frequently reported tumours are villous adenomas. Dehydration with severe hyponatremia, hypokalemia, metabolic acidosis, acute renal failure and watery diarrhoea is typical. The authors present a case of McKittrick-Wheelock syndrome caused by rectal adenocarcinoma.


Subject(s)
Adenocarcinoma/complications , Diarrhea/etiology , Rectal Neoplasms/complications , Adenocarcinoma/surgery , Diarrhea/therapy , Fluid Therapy/methods , Humans , Isotonic Solutions/therapeutic use , Male , Middle Aged , Rectal Neoplasms/surgery , Syndrome , Treatment Outcome , Water-Electrolyte Imbalance/complications , Water-Electrolyte Imbalance/therapy
4.
J Infect ; 52(3): 223-6, 2006 Mar.
Article in English | MEDLINE | ID: mdl-15904966

ABSTRACT

Cogan's syndrome is often preceded by upper respiratory tract symptoms. The only reported specific agent possibly involved in pathogenesis of the Cogan's syndrome was Chlamydia pneumoniae. Positive IgA, IgM and IgG antibodies against C. pneumoniae in our patient suggest possibility of Chlamydia's role as a trigger for the vasculitis.


Subject(s)
Autoimmune Diseases/etiology , Chlamydophila Infections/complications , Chlamydophila pneumoniae/isolation & purification , Adult , Anti-Inflammatory Agents/therapeutic use , Autoimmune Diseases/drug therapy , Chlamydophila Infections/drug therapy , Cyclophosphamide/therapeutic use , Humans , Immunosuppressive Agents/therapeutic use , Male , Methylprednisolone/therapeutic use
5.
J Infect ; 51(2): E15-8, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16038742

ABSTRACT

Idiopathic CD4+T-lymphocytopenia (ICL) is a syndrome characterised by the depletion in the CD4+T-cells but without evidence of HIV infection. Aside from low CD4+lymphocyte counts, the immunologic findings in these patients are distinct from the abnormalities found in HIV infection. There are numerous reports of ICL associated with different diseases and clinical conditions. Opportunistic infections, mostly seen in HIV patients are the most common among them. We describe two patients without risk factors for human immunodeficiency virus (HIV) infection, each of whom presented with cryptococcal meningitis and was found to have idiopathic CD4+T-lymphocytopenia. One of them also acquired EBV and CMV coinfection of the central nervous system.


Subject(s)
Meningitis, Cryptococcal/complications , Meningitis, Cryptococcal/diagnosis , T-Lymphocytopenia, Idiopathic CD4-Positive/complications , T-Lymphocytopenia, Idiopathic CD4-Positive/diagnosis , Adult , Aged , Cytomegalovirus Infections/complications , Cytomegalovirus Infections/diagnosis , Epstein-Barr Virus Infections/complications , Epstein-Barr Virus Infections/diagnosis , Fatal Outcome , Female , Humans , Male , Meningitis, Cryptococcal/drug therapy , Meningitis, Cryptococcal/microbiology , T-Lymphocytopenia, Idiopathic CD4-Positive/drug therapy , T-Lymphocytopenia, Idiopathic CD4-Positive/microbiology , Treatment Outcome
6.
Scand J Infect Dis ; 36(6-7): 524-7, 2004.
Article in English | MEDLINE | ID: mdl-15307593

ABSTRACT

Cogan's syndrome is a rare autoimmune multisystem disease. The main clinical features of typical Cogan's syndrome are vestibuloauditory dysfunction and interstitial keratitis. The authors present a case of atypical Cogan's syndrome with headache, fever, deafness, trigeminal neuralgia and electroencephalographic abnormality which mimicked viral encephalitis.


Subject(s)
Encephalitis, Viral/physiopathology , Adult , Conjunctivitis/etiology , Deafness/etiology , Electroencephalography , Fever/etiology , Headache/etiology , Humans , Male , Syndrome , Trigeminal Neuralgia/etiology
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