516.8 ALVEOL PNEUMONOPATHY NEC


Code Information

Diagnosis Code: 516.8

Short Description: Alveol pneumonopathy NEC

Long Description: Other specified alveolar and parietoalveolar pneumonopathies

Code Classification:

  • Diseases of the respiratory system (460–519)
    • Other diseases of respiratory system (510-519)
      • 516 Other alveolar and parietoalveolar pneumopathy
        • 516.8 Alveol pneumonopathy NEC

Code Version: 2015 ICD-9-CM


Synonyms

  • Bronchiolitis obliterans organizing pneumonia
  • Cholesterol pneumonia
  • Desquamative interstitial pneumonia
  • Endogenous lipoid pneumonia
  • Giant cell interstitial pneumonitis
  • Human immunodeficiency virus disease resulting in lymphoid interstitial pneumonitis
  • Interstitial pneumonia
  • Lymphoid interstitial pneumonia
  • Nonspecific interstitial pneumonia
  • Primary atypical interstitial pneumonia
  • Seasonal cryptogenic organizing pneumonia with biochemical cholestasis

References to Index of Diseases and Injuries

The code 516.8 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Block
    • alveolar capillary 516.8
  • BOOP (bronchiolitis obliterans organized pneumonia)� 516.8
  • Bronchiolitis (acute) (infectious) (subacute) 466.19
    • obliterans 491.8
      • with organizing pneumonia (BOOP) 516.8
  • Fibrosis, fibrotic
    • pulmonary (chronic) (see also Fibrosis, lung) 515
      • alveolar capillary block 516.8
  • Pneumonia (acute) (Alpenstich) (benign) (bilateral) (brain) (cerebral) (circumscribed) (congestive) (creeping) (delayed resolution) (double) (epidemic) (fever) (flash) (fulminant) (fungoid) (granulomatous) (hemorrhagic) (incipient) (infantile) (infectious) (infiltration) (insular) (intermittent) (latent) (lobe) (migratory) (newborn) (organized) (overwhelming) (primary) (progressive) (pseudolobar) (purulent) (resolved) (secondary) (senile) (septic) (suppurative) (terminal) (true) (unresolved) (vesicular) 486
    • bronchiolitis obliterans organized (BOOP) 516.8
    • broncho-, bronchial (confluent) (croupous) (diffuse) (disseminated) (hemorrhagic) (involving lobes) (lobar) (terminal) 485
      • lipid 507.1
        • endogenous 516.8
    • cholesterol 516.8
    • interstitial 516.8
      • with influenzal (see also Influenza) 487.0
      • acute
        • due to Pneumocystis (carinii) (jiroveci) 136.3
          • meaning:
            • acute interstitial pneumonitis 516.33
            • atypical pneumonia - see Pneumonia, atypical
            • bacterial pneumonia - see Pneumonia, bacterial
      • chronic (see also Fibrosis, lung) 515
      • desquamative 516.37
      • hypostatic 514
      • idiopathic 516.30
        • lymphoid 516.35
      • lipoid 507.1
      • lymphoid (due to known underlying cause) 516.8
      • non-specific (due to known underlying cause) 516.8
      • organizing (due to known underlying cause) 516.8
      • plasma cell 136.3
      • Pseudomonas 482.1
    • lipid, lipoid (exogenous) (interstitial) 507.1
      • endogenous 516.8
  • Pneumonitis (acute) (primary) (see also Pneumonia) 486
    • cholesterol 516.8
    • interstitial (chronic) (see also Fibrosis, lung) 515
      • lymphoid 516.8
    • lymphoid, interstitial 516.8
  • Pneumopathy NEC 518.89
    • alveolar 516.9
    • parietoalveolar 516.9
      • specified condition NEC 516.8
  • Syndrome - see also Disease
    • alveolar capillary block 516.8

Crosswalk Information

The code 516.8 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
516.8 Right Arrow J84.09 Other alveolar and parieto-alveolar conditions
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
516.0 Pulmonary alveolar proteinosis
516.1 Idiopathic pulmonary hemosiderosis
516.2 Pulmonary alveolar microlithiasis
516.30 Idiopathic interstitial pneumonia, not otherwise specified
516.31 Idiopathic pulmonary fibrosis
516.32 Idiopathic non-specific interstitial pneumonitis
516.33 Acute interstitial pneumonitis
516.34 Respiratory bronchiolitis interstitial lung disease
516.35 Idiopathic lymphoid interstitial pneumonia
516.36 Cryptogenic organizing pneumonia
516.37 Desquamative interstitial pneumonia
516.4 Lymphangioleiomyomatosis
516.5 Adult pulmonary Langerhans cell histiocytosis
516.61 Neuroendocrine cell hyperplasia of infancy
516.62 Pulmonary interstitial glycogenosis
516.63 Surfactant mutations of the lung
516.64 Alveolar capillary dysplasia with vein misalignment
516.69 Other interstitial lung diseases of childhood
516.9 Unspecified alveolar and parietoalveolar pneumonopathy


This page was last updated on: 10/1/2014