STAGING AND CLINICAL 
MANIFESTATION OF HIV
 HIV classification system is used to 
categorize the stage of paediatric disease by 
using two parameters: 
 clinical status 
 degree of immunologic impairment.
REVISED WHO CLINICAL 
STAGING OF HIV/AIDS 
FOR INFANTS AND 
CHILDREN
 Asymptomatic 
 PGL (persistent generalized 
lymphadenopathy)
 Hepatosplenomegaly 
 Papular pruritic eruptions 
 Seborrhoeic dermatitis
 Extensive human papilloma virus 
infection(condyloma acuminata)
 Extensive molluscum contagiosum 
 Fungal nail infections 
 Recurrent or chronic RTIs (otitis media, 
otorrhoea, sinusitis)
 Recurrent oral ulcerations 
 Linear gingival erythema (LGE) 
 Angular cheilitis
 Parotid enlargement 
 Herpes zoster
Conditions where a presumptive diagnosis 
can be made on the basis of clinical signs or 
simple investigations 
 Moderate unexplained malnutrition not 
adequately responding to standard therapy 
 Unexplained persistent diarrhoea (14 days or 
more ) 
 Unexplained persistent fever (intermittent or 
constant, for longer than one month)
 Oral candidiasis (outside neonatal period ) 
 Severe recurrent presumed bacterial 
pneumonia
 Oral hairy leukoplakia 
 Pulmonary TB
 Acute necrotizing ulcerative 
gingivitis/periodontitis
Conditions where confirmatory diagnostic 
testing is necessary 
 Chronic HIV-associated lung disease 
including brochiectasis 
 Lymphoid interstitial pneumonitis (LIP) 
 Unexplained anaemia (<8g/dl), and or 
neutropenia (<1000/mm3) and 
thrombocytopenia (<50 000/ mm3) for more 
than one month
Conditions where a presumptive diagnosis 
can be made on the basis of clinical signs or 
simple investigations 
 Unexplained severe wasting or severe 
malnutrition not adequately responding to 
standard therapy 
 Pneumocystis pneumonia
 Recurrent severe presumed bacterial 
infections (e.g. empyema, pyomyositis, bone 
or joint infection, meningitis, but excluding 
pneumonia) 
 HIV encephalopathy 
 Extrapulmonary TB 
 CNS toxoplasmosis (outside the neonatal 
period)
 Chronic herpes simplex infection; (orolabial 
or cutaneous of more than one month’s 
duration)
 Kaposi’s sarcoma 
 Oesophageal candidiasis
Conditions where confirmatory diagnostic 
testing is necessary 
 CMV infection (CMV retinitis or infection of 
organs other than liver, spleen or lymph 
nodes; onset at age one month or more)
 Extrapulmonary cryptococcosis including 
meningitis 
 Any disseminated endemic mycosis (e.g. 
extrapulmonary histoplasmosis, 
coccidiomycosis,penicilliosis) 
 Cryptosporidiosis 
 Isosporiasis
 Disseminated non-tuberculous mycobacteria 
infection 
 Progressive multifocal leukoencephalopathy 
(PML) 
 Candida of trachea, bronchi or lungs 
 HIV-associated cardiomyopathy or HIV-associated 
nephropathy
 Visceral herpes simplex infection 
 Acquired HIV associated rectal fistula 
 Cerebral or B cell non-Hodgkin lymphoma
IMMUNE STATUS Age 
Up to 12 
months 
13-59 
months 
5 years or 
over 
Not significant 
immunosuppression 
>35% >25% >500/mm3 
Mild immunosuppression 25−34% 20−24% 350−499/m 
m3 
Advanced 
immunosuppression 
20−24% 15−19% 200−349/m 
m3 
Severe immunosuppression <20% <15% <200/mm3

Staging and clinical manifestation of HIV

  • 1.
    STAGING AND CLINICAL MANIFESTATION OF HIV
  • 2.
     HIV classificationsystem is used to categorize the stage of paediatric disease by using two parameters:  clinical status  degree of immunologic impairment.
  • 3.
    REVISED WHO CLINICAL STAGING OF HIV/AIDS FOR INFANTS AND CHILDREN
  • 4.
     Asymptomatic PGL (persistent generalized lymphadenopathy)
  • 5.
     Hepatosplenomegaly Papular pruritic eruptions  Seborrhoeic dermatitis
  • 6.
     Extensive humanpapilloma virus infection(condyloma acuminata)
  • 7.
     Extensive molluscumcontagiosum  Fungal nail infections  Recurrent or chronic RTIs (otitis media, otorrhoea, sinusitis)
  • 8.
     Recurrent oralulcerations  Linear gingival erythema (LGE)  Angular cheilitis
  • 9.
     Parotid enlargement  Herpes zoster
  • 10.
    Conditions where apresumptive diagnosis can be made on the basis of clinical signs or simple investigations  Moderate unexplained malnutrition not adequately responding to standard therapy  Unexplained persistent diarrhoea (14 days or more )  Unexplained persistent fever (intermittent or constant, for longer than one month)
  • 11.
     Oral candidiasis(outside neonatal period )  Severe recurrent presumed bacterial pneumonia
  • 12.
     Oral hairyleukoplakia  Pulmonary TB
  • 13.
     Acute necrotizingulcerative gingivitis/periodontitis
  • 14.
    Conditions where confirmatorydiagnostic testing is necessary  Chronic HIV-associated lung disease including brochiectasis  Lymphoid interstitial pneumonitis (LIP)  Unexplained anaemia (<8g/dl), and or neutropenia (<1000/mm3) and thrombocytopenia (<50 000/ mm3) for more than one month
  • 15.
    Conditions where apresumptive diagnosis can be made on the basis of clinical signs or simple investigations  Unexplained severe wasting or severe malnutrition not adequately responding to standard therapy  Pneumocystis pneumonia
  • 16.
     Recurrent severepresumed bacterial infections (e.g. empyema, pyomyositis, bone or joint infection, meningitis, but excluding pneumonia)  HIV encephalopathy  Extrapulmonary TB  CNS toxoplasmosis (outside the neonatal period)
  • 17.
     Chronic herpessimplex infection; (orolabial or cutaneous of more than one month’s duration)
  • 18.
     Kaposi’s sarcoma  Oesophageal candidiasis
  • 19.
    Conditions where confirmatorydiagnostic testing is necessary  CMV infection (CMV retinitis or infection of organs other than liver, spleen or lymph nodes; onset at age one month or more)
  • 20.
     Extrapulmonary cryptococcosisincluding meningitis  Any disseminated endemic mycosis (e.g. extrapulmonary histoplasmosis, coccidiomycosis,penicilliosis)  Cryptosporidiosis  Isosporiasis
  • 21.
     Disseminated non-tuberculousmycobacteria infection  Progressive multifocal leukoencephalopathy (PML)  Candida of trachea, bronchi or lungs  HIV-associated cardiomyopathy or HIV-associated nephropathy
  • 22.
     Visceral herpessimplex infection  Acquired HIV associated rectal fistula  Cerebral or B cell non-Hodgkin lymphoma
  • 23.
    IMMUNE STATUS Age Up to 12 months 13-59 months 5 years or over Not significant immunosuppression >35% >25% >500/mm3 Mild immunosuppression 25−34% 20−24% 350−499/m m3 Advanced immunosuppression 20−24% 15−19% 200−349/m m3 Severe immunosuppression <20% <15% <200/mm3