Primary Pulmonary Mucinous Cystadenocarcinoma: A Case Report

Author:

Efstathiou Andreas1,Asteriou Christos1,Barbetakis Nikolaos1,Miliaras Dimosthenis2,Kleontas Athanassios1,Karvelas Christos1,Lalountas Miltiadis3

Affiliation:

1. Cardiothoracic Surgery Department, Theagenio Cancer Hospital, Al. Symeonidi 2, 54007 Thessaloniki, Greece

2. Laboratory of Histology and Embryology, Medical School, Aristotle University of Thessaloniki, 54636 Thessaloniki, Greece

3. 2nd Propedeutical Department of Surgery, Hippokration General Hospital, Aristotle University of Thessaloniki, Konstantinoupoleos 49, 54642 Thessaloniki, Greece

Abstract

Primary pulmonary mucinous cystadenocarcinoma (PMCAC) is an extremely rare cystic neoplasm. A case of a 56-year-old male with a cystic lesion of the right lower lobe is described. Preoperative fine needle aspiration cytology and bronchoscopy were inconclusive. The patient underwent a formal right lower lobectomy and mediastinal lymph node dissection. Diagnosis was established intraoperatively. The biological behavior of primary PMCAC is unknown. Therefore, careful long-term follow-up is considered necessary because of lack of experience globally.

Publisher

Hindawi Limited

Subject

General Medicine

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