Manasrah Janaa, Fasfoos Ahmad, Jabareen Maaweya, Alhroub Wasef, Asbeh Yousef Abu
Faculty of Medicine, Hebron University, Hebron, Palestine.
Faculty of Medicine, Hebron University, Hebron, Palestine.
Int J Surg Case Rep. 2025 Apr;129:111120. doi: 10.1016/j.ijscr.2025.111120. Epub 2025 Mar 4.
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.
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.
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.
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.
该患者术后恢复顺利,凸显了早期干预对罕见先天性异常管理的重要性。支气管囊肿占先天性囊性肺病的13 - 15%,占儿童纵隔肿物的6%。这些囊肿源于胚胎发育过程中前肠的异常发育,可无症状或引发严重并发症,如气道或血管受压。
一名10日龄女婴,产前常规超声检查发现左上肺叶有一个肺囊性病变。她出生时无症状,无呼吸窘迫或先天性异常。胸部CT显示一个大的双房囊肿,导致肺受压和纵隔移位。初步诊断提示为1型先天性肺气道畸形(CPAM)。电视辅助胸腔镜手术(VATS)成功切除病变,组织病理学证实为支气管囊肿。
支气管囊肿由胚胎发育过程中前肠的异常芽生形成,通常表现为与支气管树无相通的单房囊肿。虽然这些囊肿通常无症状,但由于压迫效应可导致危及生命的并发症。包括产前超声、胎儿MRI和产后CT扫描在内的影像学检查对诊断至关重要。组织病理学通过识别特征性的纤毛假复层柱状上皮来提供确诊依据。必须排除诸如CPAM或肺隔离症等鉴别诊断。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。
本病例强调了支气管囊肿早期诊断和及时手术治疗的重要性。即使对无症状婴儿,及时干预也能确保成功康复并预防危及生命的并发症。