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1.
Clin Toxicol (Phila) ; 46(2): 153-5, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17917867

ABSTRACT

INTRODUCTION: Heroin overdose can cause various rare neurological complications like spongiform leukoencephalopathy, seizures, stroke, toxic amblyopia, transverse myelopathy, mononeuropathy, plexopathy, acute inflammatory demyelinating polyradiculoneuropathy, rhabdomyolysis, compartment syndrome, fibrosing myopathy, and acute bacterial myopathy. We report here the simultaneous presentation of multiple complications of heroin toxicity. CASE REPORT: A young heroin addict was found unarousable lying in the lotus posture. Examination showed quadriplegia and left leg gangrene. He subsequently developed heroin-induced transverse myelitis, rhabdomyolysis, left leg compartment syndrome, and myoglobin-induced acute renal failure. DISCUSSION: This case leads us to consider a common linked or systemic mechanism of injury rather than a local mechanism when multiple simultaneous organ failure occurs complicating heroin abuse.


Subject(s)
Acute Kidney Injury/etiology , Compartment Syndromes/etiology , Heroin Dependence/complications , Myelitis, Transverse/etiology , Rhabdomyolysis/etiology , Adult , Gangrene/etiology , Humans , Male , Quadriplegia/etiology , Unconsciousness/etiology
2.
J Med Microbiol ; 56(Pt 8): 1101-1106, 2007 Aug.
Article in English | MEDLINE | ID: mdl-17644719

ABSTRACT

Sixty symptomatic confirmed human immunodeficiency virus (HIV)-positive adult patients, of both sexes, suspected of having a fungal infection were taken as a study population, and the clinicomycological profile was correlated with the immunological status of the patients with particular reference to CD4 counts. Relevant samples were collected and subjected to direct microscopy, fungal culture and serology. CD4 counts were determined by flow cytometry. Patients belonged to the age group of 17-65 years, with a male : female ratio of 4.8 : 1. Heterosexuality was the commonest mode of transmission. Candidiasis was the most common diagnosis (41.7 %), followed by cryptococcosis (10.0 %), and pneumocystinosis and aspergillosis (8.3 % each). Two cases of histoplasmosis were also diagnosed. A low mean CD4 count of <200 cells microl(-1) was seen with most fungal infections. A total of 73 % of patients belonged to World Health Organization (WHO) stage 4, while 23.33 % belonged to stage 3. Thirty one patients (51.67 %) belonged to Centers for Disease Control and Prevention (CDC) stage C3. Various fungal infections correlated well with the mean CD4 counts. It was difficult to correlate statistically WHO and CDC staging because of the small sample size. However, it was possible to assess to a limited extent the possibility of using clinical diagnosis to predict the status of progression of HIV infection in a resource-poor outpatient setting.


Subject(s)
AIDS-Related Opportunistic Infections/epidemiology , Mycoses/epidemiology , AIDS-Related Opportunistic Infections/diagnosis , AIDS-Related Opportunistic Infections/immunology , AIDS-Related Opportunistic Infections/microbiology , Adolescent , Adult , Aged , Aspergillosis/epidemiology , Aspergillosis/microbiology , Aspergillus niger/isolation & purification , CD4 Lymphocyte Count , Candida/isolation & purification , Candidiasis/epidemiology , Candidiasis/microbiology , Cryptococcosis/epidemiology , Cryptococcosis/microbiology , Cryptococcus neoformans/isolation & purification , Disease Progression , Female , HIV , Heterosexuality , Hospitals, Special , Humans , India/epidemiology , Male , Middle Aged , Mycoses/microbiology , Sexual Partners
4.
Indian J Pathol Microbiol ; 47(1): 29-32, 2004 Jan.
Article in English | MEDLINE | ID: mdl-15471120

ABSTRACT

Congenital cystic adenomatoid malformation (CCAM) of the lung is a rare anomaly of fetal development of terminal respiratory structures. We report three cases of congenital cystic adenomatoid malformation (CCAM) of lung Stocker's type I. All the cases presented with progressive neonatal respiratory distress. One case developed hyaline membrane because of ventilator therapy. No other congenital malformation was found in any of our cases. Two of our cases were suspected on antenatal ultrasonography. Routine prenatal ultrasonography has increased the frequency of prenatal diagnosis of congenital cystic lung malformation including CCAM. The pathogenesis, management and prognosis of CCAM are discussed along with a review of literature.


Subject(s)
Cystic Adenomatoid Malformation of Lung, Congenital/pathology , Cystic Adenomatoid Malformation of Lung, Congenital/diagnostic imaging , Female , Humans , Infant, Newborn , Lung/pathology , Male , Pregnancy , Ultrasonography, Prenatal
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