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Korean Journal of Nuclear Medicine ; : 277-280, 2017.
Article in English | WPRIM | ID: wpr-786927

ABSTRACT

A 63-year-old male with a recently diagnosed right lung lesion was referred for staging. F-FDG PET/CT scan revealed a hypodense, cystic-like mass in the right upper lung lobe, which demonstrated low, diffuse ¹⁸F-FDG uptake, likely due to the presence of mucus, as well as intensely hypermetabolic right hilar and right paratracheal lymph nodes. Transbronchial biopsy revealed a primary pulmonary mucinous cystadenocarcinoma with the presence of signet ring cell carcinoma, a co-existence of two rare variants of lung adenocarcinoma. This case report demonstrates the metabolic phenotype along with the radiographic characteristics of this rare tumor and its metastases.


Subject(s)
Humans , Male , Middle Aged , Adenocarcinoma , Biopsy , Carcinoma, Signet Ring Cell , Cystadenocarcinoma, Mucinous , Fluorodeoxyglucose F18 , Lung , Lung Neoplasms , Lymph Nodes , Mucins , Mucus , Neoplasm Metastasis , Phenotype , Positron-Emission Tomography , Positron Emission Tomography Computed Tomography
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