A 62-year-old male with a 30-pack-year smoking habit was admitted to our clinic with dyspnea. A chest computed tomography (CT) scan revealed a spiculated mass with enhancement in the left upper lobe (LUL;
Fig. 1A) and concurrent multiple pulmonary nodules (
Fig. 1B). 2-Deoxy-2-[
18F]-fluorodeoxyglucose (FDG) positron emission tomography (PET)/CT demonstrated FDG avidity in LUL nodule (
Fig. 1C).
The patient underwent thoracoscopic wedge resection of LUL nodule and histopathology revealed a chronic granulomatous inflammation associated with several yellow-brown and ovoid eggs with a thick shell, all of which were characteristic attributes of pulmonary
Paragonimus westermani infection (
Fig. 2A). The patient did not reveal any special diet containing raw or undercooked fish. Blood
P. westermani antibodies were positive and serum total Ig-E level was elevated up to 1,663.1 UI/mL. Based on these findings, the patient was treated with praziquantel. At the same time, 1.9 cm FDG-avid lesion in left submandibular gland was detected during the work-up. However, further evaluation on the lesion was impossible owing to patient’s refusal.
Five months after treatment, follow-up high-resolution computed tomography (HRCT) images showed increased size of remnant pulmonary nodules (
Fig. 2B) and in follow-up FDG-PET/CT scan, some nodules had augmented metabolism (
Fig. 2C). Wedge resection of remaining FDG-avid nodules in the superior lingular segment revealed that it was poorly differentiated metastatic carcinoma which had a hyperchromatic and pleomorphic nuclei (
Fig. 2D). Results from PET/CT scans demonstrated increased FDG avidity in the submandibular gland, suggesting presence of primary malignancy in this area (
Fig. 2E). Finally, excisional biopsy of the submandibular gland confirmed carcinoma ex pleomorphic adenoma which appeared as pleomorphic tumor cell infiltrating into the benign adenoma (
Fig. 2F).
Herein, we demonstrated an extremely rare case of metastatic lung cancer originating from salivary gland concurrent with parasitic lung infection. Even though paragonimiasis has been frequently reported to mimic primary lung cancer [
1–
3], the possibility for the coexistence of paragonimiasis with malignant lung lesion from various origins should not be overlooked in clinical practice.