Tovi F, Mares A J
Am J Surg. 1978 Nov;136(5):631-7. doi: 10.1016/0002-9610(78)90324-0.
Cervical thymic anomalies are not as rare as previously suggested. Six cases were encountered over a relatively short period of time, prompting us to report them and emphasize the importance of this entity. Five of the six patients were children, two of them infants less than one year old. The occurrence of thymic remnants in the neck of young children is not surprising, considering the nature and behavior of the thymus at different stages of life. After a brief embryologic survey, the various types of cervical thymus (solitary ectopic, cystic, or partially arrested descent) and their pathogenesis are discussed. The rare occurrence of thyroid and parathyroid tissue within the mass of a large cervical thymic cyst is reported and evaluated. Cervical thymic lesions can either be symptomless or cause severe dyspnea and dysphagia, especially in the young infant. Accurate diagnosis and an intelligent surgical approach in the child with a cervical mass can avoid the obvious parental apprehension and lead to the correct treatment. Symptoms due to pressure on neighoring structures are promptly eliminated after excision, and prognosis is excellent.
颈部胸腺异常并不像之前认为的那样罕见。在相对较短的时间内就遇到了6例,这促使我们报告这些病例并强调这一实体的重要性。6例患者中有5例是儿童,其中2例是不到1岁的婴儿。考虑到胸腺在生命不同阶段的性质和行为,幼儿颈部出现胸腺残余并不奇怪。在进行简短的胚胎学概述后,讨论了各种类型的颈部胸腺(孤立性异位、囊性或部分发育停滞)及其发病机制。报告并评估了在巨大颈部胸腺囊肿肿块内罕见出现甲状腺和甲状旁腺组织的情况。颈部胸腺病变可以无症状,也可导致严重的呼吸困难和吞咽困难,尤其是在幼儿中。对于有颈部肿块的儿童,准确的诊断和明智的手术方法可以避免家长明显的担忧并实现正确的治疗。切除后,因对邻近结构的压迫而产生的症状会迅速消除,预后良好。