Department of Radiology, National Center for Child Health and Development, Tokyo, Japan.
Department of Pediatrics, Yamanashi Prefectural Central Hospital, Kofu-shi, Yamanashi-ken, Japan.
Pediatr Int. 2020 Nov;62(11):1234-1240. doi: 10.1111/ped.14307. Epub 2020 Nov 9.
Congenital unilateral pulmonary vein atresia (CUPVA) is known to lead to the formation of an abnormal confluent mediastinal and hilar soft tissue mass, thoracic hypoplasia, and interlobular septal thickening on the affected side. The purpose of the present study is to investigate the frequency and severity of mediastinal soft tissue mass-like lesions and examine other abnormal findings associated with CUPVA.
We retrospectively reviewed seven children with CUPVA who underwent contrast-enhanced CT scans and measured the soft tissue mass volume in the bilateral mediastinum (affected and normal side). The location of abnormal soft tissue was divided into three anatomical sections (paratracheal, peribronchial, and the dorsal aspect of the left atrium). The relationships among soft tissue volume and anatomical section were statistically evaluated. Also, the presence of thoracic hypoplasia, small ipsilateral pulmonary arteries, interlobular septal thickening, and ground-glass opacities were investigated.
In all cases, CT scans confirmed the presence of confluent soft tissue mass-like lesions in the affected mediastinum. The soft tissue volume on the affected side was 5.5-fold greater than the volume on the normal side (average: 18.0 cm and 4.25 cm respectively, P < 0.01). Thoracic hypoplasia and interlobular septal thickening were found in all patients. Small pulmonary arteries and ground-glass opacities were present in six of the seven patients.
Abnormal mediastinal and hilar soft tissue is commonly found in patients with CUPVA. So, if we encounter the mediastinal soft tissue mass in patients with CUPVA, no further test will be indicated.
先天性单侧肺静脉闭锁(CUPVA)可导致异常融合的纵隔和肺门软组织肿块、患侧胸廓发育不全和小叶间隔增厚。本研究的目的是探讨纵隔软组织肿块样病变的频率和严重程度,并检查与 CUPVA 相关的其他异常发现。
我们回顾性分析了 7 例接受增强 CT 扫描的 CUPVA 患儿,测量了双侧纵隔(患侧和正常侧)的软组织肿块体积。异常软组织的位置分为三个解剖区域(气管旁、支气管旁和左心房背侧)。统计评估了软组织体积与解剖区域之间的关系。还研究了胸廓发育不全、同侧肺小动脉狭窄、小叶间隔增厚和磨玻璃影的存在。
在所有病例中,CT 扫描均证实了患侧纵隔存在融合的软组织肿块样病变。患侧的软组织体积是正常侧的 5.5 倍(平均分别为 18.0 cm 和 4.25 cm,P < 0.01)。所有患者均存在胸廓发育不全和小叶间隔增厚。7 例患者中有 6 例存在肺小动脉狭窄和磨玻璃影。
CUPVA 患者常存在纵隔和肺门软组织异常。因此,如果我们在 CUPVA 患者中遇到纵隔软组织肿块,无需进一步检查。