Ground-glass opacification

Ground-glass opacification/opacity (GGO) is a descriptive term referring to a hazyan 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

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)
• 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 bronchoalveolar 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
• Wegener granulomatosis
• Henoch-Schönlein purpura

See also

• ground glass nodules
• diffuse ground glass nodules