Panlobular emphysema

Description

Panlobular (panacinar) emphysema destroys the entire alveolus uniformly and is predominant in the lower half of the lungs. Panlobular emphysema generally is observed in patients with homozygous alpha1-antitrypsin deficiency.

Index terms

Panlobular emphysema
Panacinar emphysema

Inclusions

Panacinar emphysema

Exclusions from above levels

CA22 – emphysema with chronic (obstructive) bronchitis
CA22.1 – emphysematous (obstructive) bronchitis
CA81.Y – emphysema due to inhalation of chemicals, gases, fumes or vapours

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CB40.3 – emphysema mediastinal
CB40.4 – Compensatory emphysema
KB27.0 – Interstitial emphysema originating in the perinatal period
NE81 – emphysema, surgical (subcutaneous)
NF0A.7 – Traumatic subcutaneous emphysema, not elsewhere classified
01 – Certain infectious or parasitic diseases
05 – Endocrine, nutritional or metabolic diseases
18 – Complications of pregnancy, childbirth and the puerperium
19 – Certain conditions originating in the perinatal period
20 – Congenital malformations, deformations and chromosomal abnormalities
22 – Injury, poisoning or certain other consequences of external causes

Sibling codes

CA21.0 – MacLeod syndrome
CA21.2 – Centrilobular emphysema
CA21.Y – Other specified emphysema
CA21.Z – Emphysema, unspecified

Foundation entity

Panlobular emphysema – http://id.who.int/icd/entity/1480198053

Part of: CA21: Emphysema › 12: Diseases of the respiratory system