Skip to main content
Respirology Case Reports logoLink to Respirology Case Reports
. 2020 Apr 18;8(5):e00563. doi: 10.1002/rcr2.563

Miliary opacities in pulmonary sarcoidosis

Keishi Sugino 1,, Hirotaka Ono 1, Masahiro Ando 1, Seiji Igarashi 2, Atsuko Kurosaki 3, Eiyasu Tsuboi 1
PMCID: PMC7165362  PMID: 32313657

Key message

Pulmonary sarcoidosis should be considered in the differential diagnosis of miliary opacities in bilateral upper lobes predominance.

Keywords: Miliary opacity, non‐caseating epithelioid cell granuloma, sarcoidosis


We present a rare case of a 37‐year‐old woman diagnosed with pulmonary sarcoidosis who presented with unusual bilateral upper lobes miliary opacities on chest high‐resolution computed tomography.

graphic file with name RCR2-8-e00563-g002.jpg

Clinical Image

Typical radiological changes of pulmonary sarcoidosis consist of hilar lymph node enlargement and micronodules along the peribronchovascular bundles; miliary opacities are rare. A previously well 37‐year‐old female presented with a six‐month history of dry cough, fatigue, and weight loss. Serum angiotensin‐converting enzyme (ACE; 27.7 U/L) and soluble interleukin‐2 receptor (sIL‐2R; 674 U/mL) levels were elevated. Chest high‐resolution computed tomography (HRCT) revealed bilateral upper lobes miliary opacities (Fig. 1A, B). 18F‐fluorodeoxyglucose–positron emission tomography revealed mild hypermetabolism in the lung abnormalities. Examination of bronchoalveolar lavage (BAL) fluid revealed a lymphocytosis of 20.0% (normal <14%) and a normal CD4/CD8 ratio of 2.2. Sputum and BAL fluid cultures were negative for fungal, bacterial, and mycobacterial pathogens. Lung biopsy specimens from the right upper lobe obtained by video‐assisted thracoscopic surgery revealed scattered non‐caseating epithelioid cell granulomas in the alveoli and pleura, confirming the diagnosis of pulmonary sarcoidosis. After three months of treatment with oral corticosteroid, her clinical condition and chest imaging abnormalities markedly improved. In addition, serum ACE and sIL‐2R levels decreased to 10.7 U/L and 157 U/mL, respectively (Fig. 1C). The pattern of military opacities is rare in sarcoidosis (<1% of cases) 1 but should be considered in the differential diagnosis, in addition to malignancy, tuberculosis, and pneumoconiosis 2.

Figure 1.

Figure 1

Chest high‐resolution computed tomography (HRCT) revealed miliary opacities in bilateral upper lobes predominance. (A) Transverse section on chest HRCT and (B) coronal images of chest CT. (C) At three months, after corticosteroid therapy, miliary opacities in both lung fields markedly improved.

Disclosure Statement

Appropriate written informed consent was obtained for publication of this case report and accompanying images.

Acknowledgment

The authors would like to thank Akira Hebisawa (Department of Histopathology, Asahi General Hospital) for investigating histopathologically.

Sugino, K , Ono, H , Ando, M , Igarashi, S , Kurosaki, A , Tsuboi, E . (2020) Miliary opacities in pulmonary sarcoidosis. Respirology Case Reports, 8(5), e00563 10.1002/rcr2.563

Associate Editor: Nicole Goh

References

  • 1. Criado E, Sánchez M, Ramírez J, et al. 2010. Pulmonary sarcoidosis: typical and atypical manifestations at high resolution CT with pathologic correlation. Radiographics 30:1567–1586. [DOI] [PubMed] [Google Scholar]
  • 2. Taki M, Ikegami N, Konishi C, et al. 2015. Pulmonary sarcoidosis presenting with military opacities. Intern. Med. 54:2483–2486. [DOI] [PubMed] [Google Scholar]

Articles from Respirology Case Reports are provided here courtesy of Wiley

RESOURCES