Kotani Hirokazu, Ishida Tokiko, Miyao Masashi, Manabe Sho, Kawai Chihiro, Abiru Hitoshi, Omae Tadaki, Osamura Toshio, Tamaki Keiji
Department of Forensic Medicine, Kyoto University Graduate School of Medicine, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Department of Forensic Medicine, Kyoto University Graduate School of Medicine, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Int J Pediatr Otorhinolaryngol. 2014 Nov;78(11):1917-22. doi: 10.1016/j.ijporl.2014.08.024. Epub 2014 Aug 26.
An ectopic cervical thymus (ECT) is regarded as a rare congenital anomaly; therefore, the optimal diagnostic and therapeutic strategy remains a debatable matter. We designed a study to elucidate the clinicopathological characteristics of ECTs in consecutive, unselected infant autopsies, to help guide case management.
We searched for ECTs in all of the 21 consecutive, unselected infant autopsy cases performed at our institution over a period of 3 years, and all ECT consensus diagnoses were confirmed by histological examination. The following clinical characteristics were evaluated in cases with ECTs: age, gender, birth week and weight, clinical symptoms due to the ECT(s), position on discovery of death, cause of death, ECT contribution to the cause of death, and concomitant congenital disorders. The anatomical features evaluated included the location, number, size, color, shape, and margins of the ECTs, and the presence of a mediastinal thymus. Histological findings of the ECT(s) and the mediastinal thymus were compared within each individual. Fusion of the parathyroid and the ECT was also investigated histologically. Spearman's rank correlation coefficient (ρ) and the corresponding P value were calculated to determine if there was an association between ECT diameter and age.
We detected 10 ECT lesions in seven cases (33%) among the 21 infant autopsy cases. The ECT cases involved five boys and two girls, with ages ranging from 1 day to 4 months. There were no reports of a positive family history of sudden death or antemortem clinical symptoms due to ECT in any of the cases. The ECTs were considered incidental regarding the cause of death, with the exception of one case that was extremely rare. Most ECTs were localized to the inferior thyroid, ranging from 0.4 to 1.9 cm in size. Size demonstrated a significant negative correlation with age (ρ=-0.75 and P=0.034).
This study revealed that ECT is an essentially benign anomaly that occurs frequently during the development of the thymus, and may disappear over the first few years of life. These results suggest a conservative approach to the management of ECTs would be appropriate.
异位颈胸腺(ECT)被视为一种罕见的先天性异常;因此,最佳的诊断和治疗策略仍是一个有争议的问题。我们设计了一项研究,以阐明连续的、未经挑选的婴儿尸检中ECT的临床病理特征,以帮助指导病例管理。
我们在3年期间于本机构进行的21例连续的、未经挑选的婴儿尸检病例中查找ECT,并通过组织学检查确认所有ECT的一致性诊断。对ECT病例的以下临床特征进行了评估:年龄、性别、出生周数和体重、ECT引起的临床症状、死亡发现时的位置、死因、ECT对死因的影响以及伴随的先天性疾病。评估的解剖学特征包括ECT的位置、数量、大小、颜色、形状和边缘,以及纵隔胸腺的存在情况。在每个个体中比较ECT和纵隔胸腺的组织学发现。还对甲状旁腺与ECT的融合进行了组织学研究。计算Spearman等级相关系数(ρ)和相应的P值,以确定ECT直径与年龄之间是否存在关联。
在21例婴儿尸检病例中,我们在7例(33%)中检测到10个ECT病变。ECT病例包括5名男孩和2名女孩,年龄范围为1天至4个月。所有病例均未报告有猝死家族史阳性或ECT引起的生前临床症状。除1例极为罕见的病例外,ECT被认为与死因无关。大多数ECT位于甲状腺下部,大小范围为0.4至1.9厘米。大小与年龄呈显著负相关(ρ=-0.75,P=0.034)。
本研究表明,ECT本质上是一种良性异常,在胸腺发育过程中经常发生,可能在生命的最初几年内消失。这些结果表明,对ECT采取保守的管理方法是合适的。