Abstract. Invasive mucinous adenocarcinoma (IMA), formerly referred to as mucinous bronchioloalveolar carcinoma, is a rare variant form of invasive adenocarcinoma and is radiologically characterized by dense pneumonic consolidation, ground-glass opacity and nodules. By contrast, large, thin-walled cysts are rare. We herein report the case of a 75-year-old man with IMA presenting as a large, irregularly shaped cystic lesion. The histological diagnosis was based on specimens obtained during a bronchoscopy. The patient underwent lobectomy followed by anticancer chemotherapy for residual intrapulmonary metastases. Of note, the small metastatic nodules transformed into cystic lesions with thin walls and fused, forming a large, multiloculated cystic lesion. Typical pneumonic consolidation appeared in the pericystic parenchyma later during the clinical course. The available literature on this rare radiological manifestation was also reviewed and discussed. Clinicians should be aware of thin-walled cystic lesions as they may be an unusual radiological finding in IMA.
IntroductionInvasive mucinous adenocarcinoma (IMA), formerly referred to as mucinous bronchioloalveolar carcinoma, is distinct from non-mucinous adenocarcinoma and has been re-classified as a variant of invasive adenocarcinoma in the International Association for the Study of Lung Cancer/American Thoracic Society/European Respiratory Society lung adenocarcinoma classification system, due to its distinct clinical, radiological and pathological characteristics, as well as its distinct genetic background (frequent KRAS mutations) (1). The typical computed tomography (CT) findings in IMA include pneumonic consolidation, ground-glass opacity and nodules; by contrast, cystic lesions are rare. We herein describe a rare case of IMA presenting as a large cystic lesion.
Case reportA 75-year-old man was admitted to the Hino Municipal Hospital due to a productive cough and mucous sputum lasting for 6 months. The patient had no previous illness or history of cigarette smoking. A chest radiograph obtained on admission revealed infiltration in the lower lobe of the right lung. A chest CT scan revealed an irregularly shaped cystic lesion comprising thin walls in the lower lobe of the right lung (9 cm in maximum diameter) and a mixed, dense and ground-glass opacity occupying a portion of the pericystic parenchyma (Fig. 1A, C and E). The tissue specimens obtained during bronchoscopy revealed non-specific inflammatory findings, without any neoplasm or vasculitis. The tissue culture was positive for Streptococcus anginosus. As treatment with antibiotics was ineffective, the CT scan was repeated one and a half months later, showing a rapid increase in the size of the cyst and progression of the parenchymal opacity in the lower lobe of the patient's right lung (Fig. 1B, D and F). In addition, centriacinar small nodules, some of which were cystic, appeared in the right middle and left upper lobes. The second-chance bronchoscopy revealed an atypical epithelium with abundant cytopl...