Shantou University Medical College, Shantou University, 22 Xinling Road, Jinping District, Shantou, 515041, China.
Department of Radiology, Shenzhen Children's Hospital, 7019 Yitian Road, Futian District, Shenzhen, 518038, China.
BMC Pediatr. 2024 Sep 28;24(1):617. doi: 10.1186/s12887-024-05069-3.
Mediastinal cystic lymphatic malformation (MCLM) in children is prone to misdiagnosis as cystic teratoma. We compared the clinical and radiologic features between the two diseases and performed a cross-comparison with previous research on adult cases. This study aims to identify characteristic pediatric manifestations to improve diagnostic accuracy.
A retrospective study of clinical and radiologic data was conducted on 12 MCLM and 20 cases of cystic teratomas confirmed by pathology or intervention biopsy. Clinical characters and radiology features (mass location and morphology, density, component, secondary complication) were recorded and compared. We reviewed clinical studies on MCLM published in the past decades, analyzing radiological differences and comparing pediatric MCLM cases at our hospital with those in the literature.
Group comparison in pediatrics between MCLM and cystic teratomas: There were significant age differences (p = 0.036), shape (p = 0.003), CT difference value (p < 0.001), CT difference ratio (p < 0.001), calcification (p < 0.001), fat (p < 0.001), and typing (p < 0.001) between the two diseases. An analysis of literature data on MCLM cases involved 16 studies.
The absence of internal fat or irregular morphology, along with a minimal CT difference value, may suggest the diagnosis of MCLM. In pediatric cases, anterior mediastinal diseases tend to extend toward the neck, and the presence of the thymus can complicate the component analysis, thereby increasing the risk of misdiagnosis. Clinical diagnosis and differential diagnosis of pediatric MCLM rely heavily on imaging evaluation.
儿童纵隔囊性淋巴管瘤(MCLM)易误诊为囊性畸胎瘤。我们比较了这两种疾病的临床和影像学特征,并与以前的成人病例研究进行了交叉比较。本研究旨在确定儿童的特征性表现,以提高诊断准确性。
对经病理或介入活检证实的 12 例 MCLM 和 20 例囊性畸胎瘤的临床和影像学资料进行回顾性研究。记录并比较了临床特征和影像学特征(肿块位置和形态、密度、成分、继发性并发症)。我们回顾了过去几十年发表的关于 MCLM 的临床研究,分析了影像学差异,并将我院的儿科 MCLM 病例与文献中的病例进行了比较。
儿科 MCLM 与囊性畸胎瘤的组间比较:年龄差异有统计学意义(p=0.036),形状差异有统计学意义(p=0.003),CT 值差异有统计学意义(p<0.001),CT 值差异比有统计学意义(p<0.001),钙化差异有统计学意义(p<0.001),脂肪差异有统计学意义(p<0.001),分型差异有统计学意义(p<0.001)。对 MCLM 病例的文献数据进行分析,共涉及 16 项研究。
缺乏内部脂肪或不规则形态,以及最小的 CT 值差异,可能提示 MCLM 的诊断。在儿科病例中,前纵隔疾病倾向于向颈部延伸,胸腺的存在会使成分分析复杂化,从而增加误诊的风险。儿童 MCLM 的临床诊断和鉴别诊断主要依赖于影像学评估。