Congenital bronchogenic cyst: A case study on early detection and surgical intervention

Janaa Manasrah , Ahmad Fasfoos , Maaweya Jabareen , Wasef Alhroub , Yousef Abu Asbeh
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Abstract

Introduction

The patient showed an uneventful recovery post-surgery, underscoring the significance of early intervention in managing rare congenital anomalies. Bronchogenic cysts constitute 13–15 % of congenital cystic lung diseases and 6 % of childhood mediastinal masses. Arising from abnormal foregut development during embryogenesis, these cysts can be asymptomatic or cause serious complications, such as airway or vascular compression.

Case presentation

A 10-day-old female newborn presented with a pulmonary cystic lesion in the left upper lung lobe, identified via routine antenatal ultrasound. She was asymptomatic at birth, with no respiratory distress or congenital anomalies. Chest CT revealed a large bilocular cyst causing lung compression and mediastinal shift. Initial diagnosis suggested Congenital Pulmonary Airway Malformation (CPAM) Type 1. Video-assisted thoracoscopic surgery (VATS) successfully removed the lesion, with histopathology confirming a bronchogenic cyst.

Discussion

Bronchogenic cysts result from abnormal budding of the foregut during embryogenesis and typically present as unilocular cysts without communication with the bronchial tree. While often asymptomatic, these cysts can cause life-threatening complications due to compression effects. Imaging modalities, including prenatal ultrasonography, fetal MRI, and postnatal CT scans, are crucial for diagnosis. Histopathology provides confirmation by identifying the characteristic ciliated pseudostratified columnar epithelium. Differential diagnoses, such as CPAM or lung sequestration, must be ruled out. Surgical excision is the gold standard treatment to prevent complications like infection, hemorrhage, or malignant transformation.

Conclusion

This case underscores the importance of early diagnosis and prompt surgical management of bronchogenic cysts. Timely intervention ensures a successful recovery and prevents life-threatening complications, even in asymptomatic infants.
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先天性支气管源性囊肿:早期发现及手术干预的个案研究
该患者术后恢复良好,强调了早期干预治疗罕见先天性异常的重要性。支气管源性囊肿占13 - 15%的先天性囊性肺病和6%的儿童纵隔肿块。由于胚胎发育过程中前肠发育异常,这些囊肿可无症状或引起严重并发症,如气道或血管受压。病例介绍:一名出生10天的女婴,通过常规产前超声发现左上肺叶肺囊性病变。她出生时无症状,没有呼吸窘迫或先天性异常。胸部CT显示一个大的双眼囊肿,引起肺压迫和纵隔移位。初步诊断为先天性肺气道畸形(CPAM) 1型。视频胸腔镜手术(VATS)成功切除病变,组织病理学证实为支气管源性囊肿。支气管囊肿是由胚胎发生时前肠异常出芽引起的,通常表现为单室囊肿,与支气管树不相通。虽然通常无症状,但由于压迫作用,这些囊肿可引起危及生命的并发症。成像方式,包括产前超声检查、胎儿MRI和产后CT扫描,对诊断至关重要。组织病理学通过鉴定特征性纤毛假层状柱状上皮提供了证实。鉴别诊断,如CPAM或肺隔离,必须排除。手术切除是预防感染、出血或恶性转化等并发症的金标准治疗方法。结论本病例强调了支气管源性囊肿的早期诊断和及时手术治疗的重要性。及时干预可确保成功康复并防止危及生命的并发症,即使对无症状婴儿也是如此。
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CiteScore
1.10
自引率
0.00%
发文量
1116
审稿时长
46 days
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