Anterior mediastinal mature teratoma in a 13-month-old girl: A case report

IF 0.2 Q4 PEDIATRICS
Gashaw Arega , Nibretu Bekele , Daniel Hailu , Fathia Omer , Michael A. Negussie , Tihitena Negussie
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Abstract

Introduction

Mature teratomas in the anterior mediastinum are rare, making up only 1–5% of mediastinal tumors. While they are usually seen in adults, it is uncommon for toddlers to have such tumors, especially large ones with concomitant pericardial effusion.

Case presentation

A 13-month-old female toddler presented with a one-month history of dry cough, progressively worsening respiratory distress, low-grade fever, intermittent rapid breathing, and non-drenching night sweats. Despite multiple evaluations and treatments for presumed hyperactive airway disease with antibiotics and salbutamol inhalers, her symptoms persisted. There was no history of prior hospitalizations, and the child was fully vaccinated with normal growth and developmental milestones. On examination, she appeared in significant respiratory distress with tachypnea, nasal flaring, subcostal and intercostal retractions, and oxygen saturation of 85 % on room air. Respiratory examination revealed decreased air entry bilaterally. Other systemic examinations were unremarkable. A chest x-ray film at the referring center revealed a mediastinal mass with an associated pleural effusion. A chest ultrasound identified a multiseptated cystic anterior mediastinal mass. A contrast-enhanced CT confirmed a 13 × 12 × 8 cm heterogeneous mass with cystic, fatty, and calcified components compressing and displacing the superior vena cava, pulmonary artery, and aorta without invasion. The trachea and mainstem bronchi were narrowed and displaced posteriorly. Serum alpha-fetoprotein and beta-human chorionic gonadotropin levels were normal, favoring a benign diagnosis. Surgical excision was performed via clamshell thoracotomy, achieving complete resection of the solid portion and aspiration of the cystic components. Histopathology confirmed a mature cystic teratoma with no immature or malignant elements. The child recovered well postoperatively, was discharged home on postoperative day seven, and is in good health at five months of follow up.

Conclusion

Large anterior mediastinal mature teratomas in toddlers are rare but manageable with early diagnosis and complete surgical resection.
13个月大女婴前纵隔成熟畸胎瘤1例
前纵隔的成熟畸胎瘤很少见,仅占纵隔肿瘤的1-5%。虽然它们通常见于成人,但在幼儿中很少有这样的肿瘤,特别是伴随心包积液的大肿瘤。病例表现:13个月大的女婴表现为一个月的干咳史,逐渐加重的呼吸窘迫,低烧,间歇性呼吸急促,非淋湿性盗汗。尽管多次评估并使用抗生素和沙丁胺醇吸入器治疗疑似气道疾病,但她的症状持续存在。既往无住院史,儿童完全接种疫苗,生长发育正常。检查时,她出现明显的呼吸窘迫,呼吸急促,鼻肿胀,肋下和肋间缩回,室内空气氧饱和度为85%。呼吸检查显示双侧进气量减少。其他全身检查无显著差异。参考中心的胸部x线片显示纵隔肿块伴胸膜积液。胸部超声检查发现一多发囊性前纵隔肿块。增强CT证实一个13 × 12 × 8厘米的非均匀肿块,有囊性、脂肪性和钙化成分压迫和移位上腔静脉、肺动脉和主动脉,但没有侵犯。气管和主支气管变窄并向后移位。血清甲胎蛋白和人绒毛膜促性腺激素水平正常,有利于良性诊断。手术切除采用翻盖开胸术,实现了实性部分的完全切除和囊性部分的抽吸。组织病理学证实为成熟囊性畸胎瘤,无未成熟或恶性成分。患儿术后恢复良好,术后第7天出院,随访5个月健康状况良好。结论幼儿前纵隔较大成熟畸胎瘤是一种罕见的疾病,早期诊断和完全手术切除是可以控制的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.60
自引率
25.00%
发文量
348
审稿时长
15 days
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