2. • ICH – special group as predisposed to both
opportunistic and non – opportunistic
organisms.
• ICH patients rising with –
- rise in incidence of HIV/AIDS.
- solid organ or bone marrow transplant.
3. SYSTEMATIC APPROACH
• History –IVDAs , CMV , Kaposi’s sarcoma.
• Examination
• Investigations – Sputum
CD4 Counts
• Chest X ray
• HRCT
• Fiberoptic bronchoscopy with BAL
9. Consolidation
Focal segmental or Lobar Air space consolidations
Characterstic Of Community acquired Pneumonias
May be seen with TB ; Rhodococcus ; Nocardia
18. Lymphadenopathy
• MC cause of mediastinal LNs – Mycobacterial Infections
• With Calcification – Disseminated PJP
• With intense enhancement – Kaposi’s Sarcoma
19. Pleural Effusion
• Massive effusion with lymphocytes on cytology – TB.
• Hemorrhagic fluid –Kaposi’s Sarcoma.
22. • Atypical fungus
• Particularly with deficiency in cell-mediated immunity.
Pathogenesis-
• P. jiroveci lives almost exclusively in the pulmonary
alveoli, adhering to the alveolar epithelium.
• Intraalveolar macrophages serve as
the primary host defense against P. jiroveci,
and macrophage deficiency or dysfunction
can lead to infection.
Pneumocystis Jeroveci Pneumonia
27. Solitary nodule or mass mimicking lung
carcinoma or as multiple nodules ranging from
a few millimeters to more than 1 cm
28. HRCT
Extensive ground-glass opacity is the principal finding in PJP.
With more advanced disease, septal lineson ground-glass opacity –crazy paving.
Consolidation.
Pulmonary cysts associated with increased frequency of spontaneous
pneumothorax
Solitary nodule or mass mimicking lung carcinoma or as multiple nodules ranging
from a few millimeters to more than 1 cm
Small nodules and tree-in-bud opacities are uncommon
Residual interstitial fibrosis - chronic Pneumocystis pneumonia .
29. MYCOBACTERIAL INFECTIONS
• HIV patients have 50 -200 times more risk of TB
• TB accelerates the progression of HIV
• CD4 > 200 – upper lobe opacity with cavitation and nodular
bronchogenic spread
• CD4 < 200 – Parenchymal consolidation , lymph nodes with
necrosis , pleural effusion , extrapulmonary spread.
34. LYMPHOCYTIC INTERSTIAL
PNEUMONITIS
HRCT
Difuse involvement
. Mediastinal lymphadenopathy
. Ground-glass change
. Scattered thin walled cysts - usually deep
within the lung parenhyma and range from 1-
30 mm (useful for differentiation between
lymphoma or the lung )
. Intersitital thickening along lymph channels
. Thickening of bronchovascular bundles
Small but variably sized pulmonary nodules (