Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report

Lung adenocarcinoma, the most common subtype of lung cancer, has been always imposed serious threat to human health. Congenital pulmonary dysplasia (CPD) lacking typical clinical manifestations is a rare developmental anomaly. Pulmonary aplasia, the rarest subtype of CPD, may present with a variety...

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Main Authors: Bo Min, Chu-xu Wang, Juan Liu, Li Gong, Cheng-xiang Wang, Xiao-hua Zuo
Format: Article
Language:English
Published: Frontiers Media S.A. 2022-11-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2022.959502/full
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author Bo Min
Chu-xu Wang
Juan Liu
Li Gong
Cheng-xiang Wang
Xiao-hua Zuo
author_facet Bo Min
Chu-xu Wang
Juan Liu
Li Gong
Cheng-xiang Wang
Xiao-hua Zuo
author_sort Bo Min
collection DOAJ
description Lung adenocarcinoma, the most common subtype of lung cancer, has been always imposed serious threat to human health. Congenital pulmonary dysplasia (CPD) lacking typical clinical manifestations is a rare developmental anomaly. Pulmonary aplasia, the rarest subtype of CPD, may present with a variety of symptoms and is frequently associated with other abnormalities. This report describes an 81-year-old woman who presented with an irritant cough. Chest computed tomography (CT) and three-dimensional (3D) reconstruction revealed an irregular mass with a diameter of 5 cm in right lower lobe adjacent to the hilum. CT also indicated a rightward mediastinal shift and the complete absence of ipsilateral upper lobar tissue with bronchus ending in a terminal cecum, resulting in a diagnosis of pulmonary aplasia. The patient accepted lobectomy and lymph node dissection without complication, histopathologic examination combined HE staining with immunohistochemistry identified the tumor as adenocarcinoma. Three months after surgery, the patient was free of respiratory symptoms without chest pain. This report highlights the necessity of comprehensive evaluation for lung malignancy concurrent with CPD and the importance of identifying the diagnosis of pulmonary dysplasia.
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spelling doaj.art-55bead3e6ce4421695aef0d2c018766d2022-12-22T03:56:55ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2022-11-011210.3389/fonc.2022.959502959502Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case reportBo Min0Chu-xu Wang1Juan Liu2Li Gong3Cheng-xiang Wang4Xiao-hua Zuo5Department of Thoracic Surgery, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaDepartment of Thoracic Surgery, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaDepartment of Anesthesiology, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaDepartment of Thoracic Surgery, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaDepartment of Thoracic Surgery, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaDepartment of Pain Management, The Affiliated Huai’an Hospital of Xuzhou Medical University and The Second People’s Hospital of Huai’an, Huai’an, Jiangsu, ChinaLung adenocarcinoma, the most common subtype of lung cancer, has been always imposed serious threat to human health. Congenital pulmonary dysplasia (CPD) lacking typical clinical manifestations is a rare developmental anomaly. Pulmonary aplasia, the rarest subtype of CPD, may present with a variety of symptoms and is frequently associated with other abnormalities. This report describes an 81-year-old woman who presented with an irritant cough. Chest computed tomography (CT) and three-dimensional (3D) reconstruction revealed an irregular mass with a diameter of 5 cm in right lower lobe adjacent to the hilum. CT also indicated a rightward mediastinal shift and the complete absence of ipsilateral upper lobar tissue with bronchus ending in a terminal cecum, resulting in a diagnosis of pulmonary aplasia. The patient accepted lobectomy and lymph node dissection without complication, histopathologic examination combined HE staining with immunohistochemistry identified the tumor as adenocarcinoma. Three months after surgery, the patient was free of respiratory symptoms without chest pain. This report highlights the necessity of comprehensive evaluation for lung malignancy concurrent with CPD and the importance of identifying the diagnosis of pulmonary dysplasia.https://www.frontiersin.org/articles/10.3389/fonc.2022.959502/fullpulmonary aplasialung adenocarcinomaCPDlung abnormalities3D CT reconstruction
spellingShingle Bo Min
Chu-xu Wang
Juan Liu
Li Gong
Cheng-xiang Wang
Xiao-hua Zuo
Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
Frontiers in Oncology
pulmonary aplasia
lung adenocarcinoma
CPD
lung abnormalities
3D CT reconstruction
title Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
title_full Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
title_fullStr Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
title_full_unstemmed Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
title_short Lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe: A case report
title_sort lung adenocarcinoma concurrent with congenital pulmonary aplasia of the right upper lobe a case report
topic pulmonary aplasia
lung adenocarcinoma
CPD
lung abnormalities
3D CT reconstruction
url https://www.frontiersin.org/articles/10.3389/fonc.2022.959502/full
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AT juanliu lungadenocarcinomaconcurrentwithcongenitalpulmonaryaplasiaoftherightupperlobeacasereport
AT ligong lungadenocarcinomaconcurrentwithcongenitalpulmonaryaplasiaoftherightupperlobeacasereport
AT chengxiangwang lungadenocarcinomaconcurrentwithcongenitalpulmonaryaplasiaoftherightupperlobeacasereport
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