Diffuse cystic lung disease due to pulmonary metastasis of bronchogenic adenocarcinoma

Tyler Overman BS, Abdurahim Aloud MD

Corresponding author: Abdurahim Aloud
Contact Information: Abdurahim.aloud@ttuhsc.edu
DOI: 10.12746/swrccc.v6i23.467

CASE

A 75-year-old woman who has never smoked presented to the clinic with a chronic daily cough. The cough was dry and occasionally productive of white phlegm; it was associated with mild dyspnea and an unintentional weight loss of 12 pounds over six months. She denied fever, chills, chest pain, and night sweats. She had no history of any exposure to tuberculosis or prior malignancy and had a negative PPD test.

Initial chest x-ray showed numerous rounded cavitary 1 cm nodules throughout both lungs mostly at the bases (Figure 1). Computed tomography of the chest showed “too numerous to count” pulmonary nodules, including cavitary nodules, focal consolidation in the left lower lobe, and few slightly enlarged hilar and mediastinal nodes (Figure 2). The differential diagnosis at the time included metastasis and infection.


Figure 1

Figure 1. Frontal radiograph of the chest shows innumerable pulmonary nodules throughout the lungs, many of which show cavitation.

Figure 2a

Figure 2b

Figure 2. Contrast axial CT images with lung and mediastinal windows shows numerous nodules throughout the lungs, a few of which show cavitation, a patchy opacity in the superior segment left lower lobe and mild right hilar and subcarinal lymphadenopathy.


A bronchoscopy with BAL and transbronchial lung biopsy was performed. Viral, fungal, bacterial, and mycobacterial cultures were negative. The initial microscopic examination of the biopsy showed papillary adenocarcinoma; the tumor cells stained positive for the immunohistochemical stains TTF1, napsin, and CK7. The biopsy specimen tested negative for CK20, CDX2, and PAX8 stains. This staining pattern was consistent with adenocarcinoma of primary pulmonary origin. The tumor cells tested positive for EGFR activation mutation associated with response to EGFR tyrosine kinase inhibitors. The tumor cells tested negative for ALK and ROS1 genes.

Computed tomography scans of the abdomen and pelvis, thyroid ultrasound, and tumor markers were ordered. The positive results included an elevated CA 19-9 and CEA; the thyroid ultrasound showed a benign-appearing 6 mm solid nodule in the inferior aspect of the left lobe and fibronodular changes throughout the thyroid gland consistent with chronic thyroiditis.

DISCUSSION

A lung cavity is defined as “a gas-filled space”, seen as lucency or low-attenuation area, within a pulmonary consolidation, a mass, or a nodule. The cavity wall thickness can vary considerably. At their end-stage presentation, some cavitary diseases may have thin walled cavities or cysts and have a continuous transition from cavities to cysts. A cyst in the lung is defined as any round circumscribed space that is surrounded by an epithelial or fibrous wall of variable thickness, usually thin walled (<2mm). It is important to distinguish a cyst from a cavity; cavities are relatively common in pulmonary cancers.

Diffuse cystic lung diseases (DCLD) are a group of disorders characterized by the presence of multiple cysts or cavitary nodules in both lungs. The differential diagnosis includes lymphangioleiomyomatosis (LAM), pulmonary Langerhans cell histiocytosis (PLCH), lymphocytic interstitial pneumonia (LIP), pulmonary amyloidosis, infections, including Pneumocystis jiroveci pneumonia, aspergilosis, septic emboli, Streptococcus pneumoniae, Staphylococcus aureus, Klebsiella pneumoniae, miliary tuberculosis, nontuberculous mycobacteria, and metastatic malignancy, including colorectal adenocarcinoma, lung adenocarcinoma, metastatic leiomyoma, and endometrial stromal sarcoma. Wall thickness and clinical information are important criteria to differentiate between cavitary and cystic lung disease. The differential diagnosis in patients with lung cysts is large. An important distinction is whether the cysts are focal or multifocal and scattered diffusely throughout both lungs, as in DCLD. In the latter case the differential diagnosis usually includes two rare entities, LAM and PLCH. Infrequently DCLD can develop as a result of metastatic malignancies, such as sarcoma, mesenchymal tumors, and colorectal or bronchogenic adenocarcinoma.

Our patient had never smoked and was generally healthy, and the diagnosis of lung cancer and PLCH seemed unlikely. Thyroid papillary adenocarcinoma was initially considered because the initial histopathological examination showed papillary adenocarcinoma, and the thyroid ultrasound showed a benign appearing 6 mm solid nodule. However, immunohistochemical staining of the tumor cells was positive for TTF1, napsin, and CK7, and was negative for CK20, CDX2, and PAX8. This staining pattern is consistent with pulmonary adenocarcinoma. Consequently, these images represent a rare presentation of metastatic bronchogenic adenocarcinoma.

Napsin A is a cytoplasmic marker identified in type II pneumocytes and alveolar macrophages and is positive in 83% of lung adenocarcinomas (ADC). It was negative in all squamous cell carcinomas in one study. In a study by Kim evaluating napsin A and TTF-1 staining of pulmonary ADC, napsin A had a positivity rate of 83% (44/53) compared to TTF-1 with a positivity rate of 57% (30/53). In addition, all non-pulmonary ADCs were negative for napsin A and TTF-1. As these studies show, TTF-1 and napsin A are both sensitive and specific for pulmonary ADC. However, napsin A recently has been reported as expressed in renal cell carcinoma, especially the papillary and clear cell types.

Keywords: cystic nodules, metastatic adenocarcinoma, bronchogenic carcinoma, napsin A

REFERENCES

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  2. Fielli M, Avila F. Diffuse cystic lung disease due to pulmonary metastasis of colorectal carcinoma. Respiratory Medicine Case Reports 2016;17:83–85. doi:10.1016/j.rmcr.2015.12.006.
  3. Siddiqui MT. TTF-1 and Napsin a double staining in diagnosing lung adenocarcinoma. J Cytol Histol 2012;3:e103. doi:10.4172/2157-7099.1000e103


From: The Department of Internal Medicine at Texas Tech University Health Sciences Center in Lubbock, TX
Submitted: 3/14/2018
Accepted: 4/10/2018
Reviewer: Eman Attaya MD
Conflicts of interest: none
This work is licensed under a Creative Commons Attribution-ShareAlike 4.0 International License.