Abstract
The pathological approach to diffuse cystic lung disease (DCLD) requires recognition of a cyst, careful histological examination of the cyst wall and adjacent lung parenchyma, exclusion of cyst mimics, and correlation with clinical and radiographic information. Using this standard approach allows definitive recognition of the etiology of the cystic lesions in most cases. This chapter reviews pathological features of common and uncommon causes of DCLDs. Salient clinical and radiographical features that assist the pathologist are discussed. Finally, pathological features of the cyst mimics are explored.
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Abbreviations
- A1ATD:
-
Alpha 1 antitrypsin deficiency
- BHD:
-
Birt-Hogg-Dube syndrome
- CLE:
-
Centrilobular emphysema
- CPAM:
-
Congenital pulmonary airway malformation
- CTD:
-
Connective tissue disease
- DCLD:
-
Diffuse cystic lung disease
- DIP:
-
Desquamative interstitial pneumonia
- ECD:
-
Erdheim-Chester disease
- ESS:
-
Endometrial stromal sarcoma
- GGO:
-
Ground-glass opacities
- HC:
-
Honeycomb cysts
- HP:
-
Hypersensitivity pneumonitis
- HPV:
-
Human papilloma virus
- HRCT:
-
High-resolution computed tomography
- LAM:
-
Lymphangioleiomyomatosis
- LCDD:
-
Light chain deposition disease
- LIP:
-
Lymphoid interstitial pneumonia
- MMPH:
-
Multifocal micronodular pneumocyte hyperplasia
- NSIP:
-
Nonspecific interstitial pneumonia
- PJP:
-
Pneumocystis jiroveci pneumonia
- PLCH:
-
Pulmonary Langerhans cell histiocytosis
- RB:
-
Respiratory bronchiolitis
- RRP:
-
Recurrent respiratory papillomatosis
- SRIF:
-
Smoking-related interstitial fibrosis
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Carney, J.M., Smith, M.L. (2021). Pathological Evaluation of Pulmonary Cysts. In: Gupta, N., Wikenheiser-Brokamp, K.A., McCormack, F.X. (eds) Diffuse Cystic Lung Diseases. Respiratory Medicine. Humana, Cham. https://doi.org/10.1007/978-3-030-63365-3_4
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