Published online Jul 6, 2019. doi: 10.12998/wjcc.v7.i13.1711
Peer-review started: February 18, 2019
First decision: March 14, 2019
Revised: March 29, 2019
Accepted: May 2, 2019
Article in press: May 3, 2019
Published online: July 6, 2019
Processing time: 138 Days and 22.5 Hours
Hepatoid adenocarcinoma (HAC) occurs in extrahepatic organs such as the gastrointestinal tract, testes, ovaries, lungs, mediastinum and pancreas, and frequently produces α-fetoprotein (AFP). HAC of the lung (HAL) is rare, characterized by difficult treatment and poor prognosis. There are no reports of HAL in Yunnan-Guizhou Plateau, China.
A 60-year-old male patient was clinically diagnosed with HAL pT3N0M0, stage IIB. Chest computed tomography revealed a 7.5 cm × 7.2 cm soft tissue mass located in the right lung upper lobe and the adjacent superior mediastinum. Right upper lobectomy was performed. The diagnosis of HAL was confirmed by pathological examination, and the patient received paclitaxel and carboplatin as adjuvant chemotherapy after surgery.
Clinical manifestations, pathological features, imaging findings, auxiliary examination, and treatment planning of HAL are presented to help clinicians improve their diagnosis and treatment.
Core tip: We present a patient with primary hepatoid adenocarcinoma of the lung (HAL) in Yungui Plateau, China. HAL is a rare tumor involving difficult treatment and poor prognosis. We discussed the clinical manifestations, pathological features, imaging findings, auxiliary examination performance and treatment planning of HAL in order to help clinicians improve their diagnosis and treatment.