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Pulmonary intestinal-type adenocarcinoma
Ryo Maeda1, Noritaka Isowa, Hideyuki Onuma
1Division of Thoracic Surgery, Matsue Red Cross Hospital, 200 Horomachi, Matsue, Shimane 690-8506, Japan. ryomaedamatsue@yahoo.co.jp
Interactive Cardiovascular and Thoracic Surgery
|January 11, 2008
Summary
This case report details a rare intestinal-type adenocarcinoma found in the lung of a 69-year-old male. Diagnosis involved imaging and cytology, confirmed by VATS surgery and histopathology.
Area of Science:
- Pulmonology
- Oncology
- Surgical Pathology
Background:
- Primary pulmonary adenocarcinomas can exhibit diverse histological subtypes.
- Intestinal-type adenocarcinoma (ITAC) is an uncommon subtype of lung adenocarcinoma.
- Accurate subtyping is crucial for prognosis and treatment strategies.
Observation:
- A 69-year-old male presented with a 2.5 cm right lower lobe lung nodule detected via CT and PET scans.
- The nodule showed high (18)F-fluorodeoxyglucose uptake, and sputum cytology was positive for adenocarcinoma.
- Video-assisted thoracic surgery (VATS) was performed for resection and lymph node dissection.
Findings:
- Histopathology revealed a tumor with tall columnar cells resembling intestinal epithelium and colorectal carcinoma.
- Immunohistochemistry showed positivity for cytokeratin 7 (CK7) and thyroid transcription factor-1 (TTF-1).
- Cytokeratin 20 (CK20) staining was negative, supporting a primary pulmonary origin.
Implications:
- This case highlights the importance of recognizing rare pulmonary ITAC.
- The diagnostic workup included advanced imaging, cytology, and detailed histopathological analysis.
- Understanding the immunophenotype (CK7+/TTF-1+/CK20-) aids in differentiating primary lung ITAC from metastatic colorectal adenocarcinoma.
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