Ground-glass opacification
Updates to Article Attributes
Body
was changed:
Ground glass opacification/opacity (GGO) is a descriptive term referring to an area of increased attenuation in the lung on computed tomography (CT) with preserved bronchial and vascular markings. It is a non-specific sign with a wide aetiology including infection, chronic interstitial disease and acute alveolar disease.
Pathology
Aetiology
Ground-glass opacities have a broad aetiology:
- normal expiration
- partial filling of air spaces
- partial collapse of alveoli
- interstitial thickening
- inflammation
- oedema
- fibrosis
- lepidic proliferation of neoplasm
Morphological froms
- focal ground glass opacification
- diffuse ground glass opacification
- isolated diffuse ground glass opacification 5
Differential diagnosis
Broadly speaking, the differential for ground-glass opacification can be split into 5:
- infectious processes (usually opportunistic)
- chronic interstitial diseases
- acute alveolar diseases
- other causes
Opportunistic infections
- pneumocystis pneumonia (PCP/PJP)
- cytomegalovirus pneumonia (CMV)
- herpes simplex virus pneumonia (HSV)
- respiratory syncytial virus bronchiolitis (RSV): type of infectious bronchiolitis
- other infectious causes
Chronic interstitial diseases
-
eosinophilic pneumonias: GGO can be seen in many of the eosinophilic pneumonias but is most commonly seen in 2
- simple pulmonary eosinophilia (SPE): nodules with a GGO halo
- idiopathic hypereosinophilic syndrome (IHS): nodules with a GGO halo
- acute eosinophilic pneumonia (AEP): bilateral patchy areas of GGO with interlobular septal thickening
- eosinophilic drug reactions: peripheral airspace consolidation and GGO
-
idiopathic interstitial pneumonias 3
- non-specific interstitial pneumonia: GGO with linear or reticular markings, micronodules, consolidation, and microcystic honeycombing
- usual interstitial pneumonia (UIP): focal GGO with macrocystic honeycombing, reticular opacities, traction bronchiectasis, and architectural distortion
- cryptogenic organising pneumonia (COP): formerly bronchiolitis obliterans with organising pneumonia (BOOP); GGO with airspace consolidation and mild bronchial dilatation
- exudative phase of acute interstitial pneumonia (AIP): diffuse lung consolidation with GGO
- respiratory bronchiolitis-associated interstitial lung disease (RB-ILD): patchy GGO centrilobular nodules and bronchial wall thickening
- desquamative interstitial pneumonia (DIP): GGO with linear or reticular opacities
- lymphoid interstitial pneumonia (LIP): GGO often in association with perivascular cystic lesions, septal thickening, and centrilobular nodules
- sarcoidosis (pulmonary manifestations of sarcoidosis)
Acute alveolar disease
-
alveolar oedema or pulmonary oedema
- cardiogenic pulmonary oedema
- adult respiratory distress syndrome (ARDS)
- other causes of non-cardiogenic pulmonary oedema
- hypersensitivity pneumonitis: especially acute and subacute forms
Other causes
- neoplastic processes with a lepidic proliferation pattern
- atypical adenomatous hyperplasia
- localised adenocarcinoma
- adenocarcinoma in situ or minimally invasive (formerly bronchioalveolar cell carcinoma)
- drug toxicity
Rare causes
- focal interstitial fibrosis: a non-neoplastic entity with a nodular ground-glass opacity that does not change over a long period of time; may be mistaken for a neoplastic process
- aspergillosis: a nodule with surrounding ground-glass opacity (CT halo sign) is rare except in severely immunocompromised patients
- thoracic endometriosis
- traumatic lung injury (pulmonary contusion)
- poisoning, e.g. acute/subacute phase of paraquat poisoning
- pulmonary cryptococcus infection: solitary or multiple pulmonary nodules with or without peripheral GGO
-
Granulomatosis with polyangiitisWegener granulomatosis - Henoch-Schönlein purpura
See also
-<li><a href="/articles/wegener-granulomatosis">Wegener granulomatosis</a></li>- +<li>Granulomatosis with polyangiitis</li>