Abstract
Background:
This article reports a case of a intralobar pulmonary sequestration (IPS) with a significantly large feeding artery aneurysm and shares the successful treatment experience.
Case presentation:
A male was diagnosed with IPS combined with a feeding artery aneurysm approximately 74 mm × 61 mm in nine years ago but refused thoracotomy at that time. The patient presented this time due to an infection, and a CT scan revealed a significant increase in the lesion size to approximately 123 mm × 100 mm. After controlling the pulmonary inflammation, the patient underwent thoracoscopic ligation of the supplying artery, followed by an open chest excision of the sequestrated pulmonary aneurysm and left lower lobectomy, and the recovery post-surgery was very good.
Conclusion:
When a sequestrated lung enlarges significantly, it is crucial to consider not only the conventional possibility of malignancy but also the rare coexistence of aneurysms. Thoracoscopic ligation of the supplying artery followed by open chest surgery is an effective treatment approach for IPS combined with a large feeding artery aneurysm.
1 Introduction
Intralobar pulmonary sequestration (IPS) is a rare congenital lung tissue developmental anomaly where a non-functional lung tissue mass exists independently outside of normal lung tissue (1). The sequestrated lung is separated from the normal airway bronchial tree and pulmonary artery, with its blood supply originating from the systemic circulation, primarily from the descending aorta (2). An arterial aneurysm refers to a sustained and localized enlargement of an artery, exhibiting a diameter that is at least 50% greater than that of the adjacent, unaffected segment of the vessel (3). Most aneurysms are asymptomatic; however, they can rupture due to factors such as trauma, emotional stress, or hypertension, leading to a high mortality rate once symptoms appear (4–6).
The combination of IPS and a feeding artery aneurysm is rare and is typically treated surgically as soon as it is discovered. However, this patient delayed surgery for 9 years, which allowed us to observe the progression of this disease. For similar cases, the main reported treatment approaches include thoracotomy (7) and hybrid surgery that consists of thoracic endovascular aortic repair (TEVAR) combined with IPS resection and left lower lobectomy via video-assisted thoracoscopic surgery (VATS) (8, 9). Reports on such cases are rare, and there are currently no guideline-based treatment methods. This case was treated without the implantation of a stent, which avoids the long-term use of anticoagulants after stent placement. Additionally, this case report provides specific information on the surgical approach and the patient's prognosis, offering an effective reference for the treatment of similar conditions.
2 Case report
A 38-year-old male was admitted due to “coughing with sputum for over 3 months and fever for more than 10 days”. Nine years ago, he was diagnosed with a left lower lobe mass, measuring approximately 74 mm × 61 mm, after a chest CT revealed lung infection (Figure 1A). Contrast-enhanced CT (Figure 1B) and aortography (Figures 1C,D) indicated the mass had a feeding artery originating from the thoracic aorta, with a thick mural thrombus and calcified plaques in the arterial wall. The widest part of the feeding artery measured about 65 mm × 43 mm, with a normal proximal diameter of approximately 12 mm, indicating vascular dilation of at least 3.6 times, which confirmed the diagnosis of IPS complicated by feeding artery aneurysm. Although doctors recommended thoracotomy, the patient refused. One year ago, the patient sought treatment for a lung infection, with a chest x-ray and CT scan (Figures 1E,F) showing the left lower lobe mass enlarged to approximately 112 mm × 82 mm. The patient again refused thoracotomy. Three months before this admission, he developed severe coughing and sputum production, along with fever and generalized muscle aches 10 days prior. Upon admission, his temperature was 38.8°C, dullness on percussion was noted in the left lower lung, and breath sounds were diminished. Laboratory findings showed a white blood cell count of 10.31 × 109/L (normal range: 4.0–10.0 × 109/L), C-reactive protein at 233.28 mg/L (normal range <2.87 mg/L). CT results (Figure 1G) indicated the mass further enlarged to approximately 137 mm × 96 mm compared to one year prior. Enhanced CT and MIP images (Figures 1H,I) showed the aneurysm's widest part measuring approximately 123 mm × 100 mm, with a normal proximal diameter around 13 mm, indicating vascular dilation of at least 7.7 times, along with a thick mural thrombus and calcified plaques. After the pulmonary infection was treated, the doctor advised the patient to undergo surgery as soon as possible to avoid life-threatening complications, and the patient ultimately consented to the surgical procedure. The doctor recommended that he undergo TEVAR combined with IPS resection and left lower lobectomy via VATS. However, he did not want to have a stent implanted, as he wished to avoid long-term or even lifelong anticoagulation therapy; therefore, the final surgical plan did not include stent implantation. The specific surgical steps are as follows: After cannulation of the femoral artery and vein to establish extracorporeal circulation, access to the thoracic cavity is obtained through the left posterior lateral sixth intercostal space. Under thoracoscopic guidance, the aorta is dissected at the T6 and T12 levels, followed by ligation of the supplying artery. Subsequently, the thoracic surgeon performs a left lower lobectomy and concurrently excises the aneurysm. One month post-operation, a follow-up CT (Figure 1J) revealed complete removal of the left lower lobe mass, with a small amount of pleural effusion observed, and the patient was recovering well.
Figure 1
3 Discussion
The prevailing theory concerning the development of pulmonary sequestration suggests that it arises from the formation of an accessory lung bud located posterior to the normal lung buds (2). Aneurysms frequently arise from cystic medial degeneration, which weakens the arterial walls (10). At the time of this visit, the size of the aneurysm was approximately 123 mm × 100 mm. As a branch artery of the thoracic aorta, this size is striking, even compared to an aortic aneurysm. Reports by Ryan et al. indicate that when the diameter of a thoracic aortic aneurysm exceeds 6 cm, the rates of death, rupture, or dissection can be as high as 15.6% (11). John et al. noted that the risk of aortic rupture or dissection sharply increases when the descending aorta's diameter reaches 6.5 cm (12). However, in this case, despite the aneurysm being so large, it remained stable for nine years without dissection or rupture, likely due to the presence of a thick mural thrombus within the aneurysm cavity and its protective effect against rupture (13). The blood flow prone to turbulence in the feeding artery of the sequestrated lung, providing a hemodynamic basis for thrombus formation (14, 15). Additionally, we speculate that the external sequestrated lung may also act as an “extra arterial wall”, somewhat limiting the expansion of the aneurysm. The mural thrombus and the sequestrated lung improve the feeding artery's capacity to withstand high pressure and compensate. Nonetheless, the aneurysm continues to grow and will eventually rupture, leading to mortality. Thus, the patient is both unfortunate and fortunate. Although IPS poses a health risk, the sequestrated lung and the mural thrombus serve as protective factors that limit the rupture of the aneurysm. This reflects the interbalancing, multifaceted, and complex nature of diseases, indicating that the perceptions of good and bad in relation to diseases are not fixed. The clinical thoracoscopic combined open surgery excision of the patient's lesion was highly successful. Compared to a smaller sequestrated lung lesion associated with a feeding artery aneurysm (103 mm × 72 mm) (8), this patient did not require the placement of a stent. This allows patients to avoid the need for long-term or lifelong anticoagulation therapy after surgery, making it a better treatment option for them, which provides insights for the treatment of similar cases in the future.
4 Conclusion
When a IPS shows progressive enlargement, it is vital to consider not only the possibility of malignancy but also the presence of aneurysm formation and its growth in the supplying artery. We can avoid the need for a stent as much as possible by treating the disease through thoracoscopic ligation of the supplying artery and open surgery for lesion excision, thus sparing the patient from the long-term or even lifelong use of anticoagulants associated with stent implantation.
Statements
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving humans were approved by Wenzhou people's hospital, Wenzhou, Zhejiang, China. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent was obtained from the participant/patient(s) for the publication of this case report.
Author contributions
WW: Writing – original draft, Writing – review & editing. XC: Writing – original draft, Writing – review & editing. ZL: Resources, Supervision, Writing – review & editing. WCh: Conceptualization, Investigation, Writing – review & editing. SW: Conceptualization, Visualization, Writing – review & editing. WCa: Data curation, Project administration, Writing – review & editing. HW: Conceptualization, Investigation, Methodology, Writing – review & editing. YC: Conceptualization, Supervision, Writing – original draft, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
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Summary
Keywords
intralobar pulmonary sequestration, aneurysm, thoracoscope, congenital anomaly, case report
Citation
Weng W, Chi X, Liu Z, Chen W, Wang S, Cai W, Wu H and Chen Y (2025) Intralobar pulmonary sequestration complicated by a giant supplying artery aneurysm presenting for 9 years: a case report. Front. Surg. 12:1481819. doi: 10.3389/fsurg.2025.1481819
Received
02 October 2024
Accepted
16 January 2025
Published
04 February 2025
Volume
12 - 2025
Edited by
Christos Karathanos, University Hospital of Larissa, Greece
Reviewed by
Konstantinos Dakis, University Hospital of Larissa, Greece
Peter Zimmermann, Leipzig University, Germany
Updates
Copyright
© 2025 Weng, Chi, Liu, Chen, Wang, Cai, Wu and Chen.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yaomeng Chen 280998231@qq.com
ORCID Wei Weng orcid.org/0009-0008-0920-1446 Xinle Chi orcid.org/0009-0009-7833-0935 Ze Liu orcid.org/0009-0004-8367-0970 Weiqian Chen orcid.org/0000-0003-2937-1545 Yaomeng Chen orcid.org/0009-0007-4833-5044
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.