Clinical Pathology · MU Sofia

67. Pulmonary emphysema: classification, etiology, pathogenesis. Chronic obstructive diffuse emphysema.

Explains emphysema as enlargement of distal air spaces from alveolar wall destruction without fibrosis, and its link with smoking and COPD. Sets out four anatomic types (centriacinar, panacinar, distal acinar or paraseptal, irregular) with a gross photograph, a memory aid listing each type's typical patient and site, then the inhaled-toxin and elastase-driven pathogenesis with the alpha-1-antitrypsin role.

Inside: 1 section · 1 labelled picture · 15 flashcards · 2 min

Topic 67 of 138 in the MU Sofia syllabus for Clinical Pathology (Medicine, Year 4). The free AceMed note covers it in 1 section, about 316 words (2 min of reading), with 15 flashcards.

In this note

  1. Pulmonary emphysema: classification, etiology, pathogenesis. Chronic obstructive diffuse emphysema

Pulmonary emphysema: classification, etiology, pathogenesis. Chronic obstructive diffuse emphysema

Emphysema is the abnormal enlargement of the air spaces distal to the terminal bronchiole due to the destruction of alveolar walls, without fibrosis. Emphysema is most commonly associated with smoking,

and very often occurs with chronic bronchitis, the combination of the two diseases being Chronic Obstructive Pulmonary Disease (COPD).

Classification is based on anatomic distribution within the lobule:

  • Centriacinar (centrilobular) emphysema
  • Central or proximal parts of acini are affected, while distal ones are spared
  • Panacinar (panlobular) emphysema
  • Acini are uniformly enlarged, affecting all of the alveoli
  • Distal acinar (paraseptal) emphysema
  • The proximal parts of the acini are normal, while the distal part is involved
  • Irregular emphysema
  • Irregular pattern of acinar damage

Gross: centriacinar (centrilobular) emphysema in a smoker. Small holes lined by black anthracotic pigment sit at the centre of each lobule, with preserved lung around them (ruler in cm).

Image: “Centrilobular emphysema 865 lores” by Dr. Edwin P. Ewing, Jr., Public domain, via Wikimedia Commons.

Remember: each type has its typical patient and site:

  • Centriacinar: heavy smokers, worst in the upper lobes and apical segments (over 95% of clinical cases)
  • Panacinar: α1-antitrypsin deficiency, worst in the lower lobes
  • Paraseptal: next to the pleura and septa; ruptured subpleural cysts cause spontaneous pneumothorax in young adults

Etiology and pathogenesis

  • Exposure to toxic substances are inhaled, and induce ongoing inflammation with accumulation of neutrophils, macrophages and lymphocytes in the lung
  • elastases , cytokines and oxidants are released causing epithelial injury and proteolysis of the ECM
  • Elastin degradation products further increase inflammation
  • A genetic loss of alpha 1-antitrypsin exacerbated the issue

Diagnosis and classification is based on macroscopic appearance of lung, with diagnosis under the microscope of alveolar destruction without fibrosis leading to enlarged air spaces. The loss of elastic tissue in the alveoli means their air cannot be properly expelled from alveoli, this makes it an obstructive disease.

GP NOTEBOOK SAYS

  • Treatment is the same as COPD above

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