Mature Cystic Teratoma of Anterior Mediastinum in a Child: A Case Report and Literature Review.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Anas M Barabrah, Basel Zaben, Anas R Tuqan, Omar Salah, Mohammad Hakam Shehadeh, Hasan Eideh, Wael Amro
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引用次数: 0

Abstract

Mediastinal mature cystic teratomas are rare benign germ cell tumors that predominantly affect children. Despite their low incidence, they present unique diagnostic and management challenges. Early recognition and appropriate surgical intervention are crucial for optimal outcomes. This case report aims to highlight the importance of prompt diagnosis and management of mediastinal mature cystic teratomas in pediatric patients. We present the case of a 10-year-old female patient who presented with persistent chest pain and dyspnea. Imaging studies, including a chest X-ray and contrast-enhanced chest CT scan, revealed a large, well-circumscribed anterior mediastinal mass with calcifications. The patient underwent a right thoracotomy, resulting in the excision of a 6 × 5 × 5 cm mature cystic teratoma. Histopathological examination confirmed the diagnosis. The patient had an uneventful recovery and was discharged in stable condition. Mediastinal mature cystic teratomas pose diagnostic challenges due to their nonspecific symptoms and heterogeneous imaging characteristics. Differential diagnosis includes other mediastinal masses containing fat and calcifications. Surgical excision is the preferred treatment, although complete removal can be challenging due to adhesions to neighboring structures. Close follow-up is necessary to monitor for recurrence and complications. Mediastinal mature cystic teratomas are rare tumors with variable clinical presentations. Early detection and surgical intervention are crucial for optimal outcomes. These tumors should be included in the list of differential diagnoses for mediastinal masses in pediatric patients.

儿童前纵隔成熟囊性畸胎瘤:病例报告与文献综述
纵隔成熟囊性畸胎瘤是一种罕见的良性生殖细胞肿瘤,主要影响儿童。尽管其发病率较低,但在诊断和管理方面却面临着独特的挑战。早期识别和适当的手术干预对获得最佳治疗效果至关重要。本病例报告旨在强调及时诊断和处理儿童纵隔成熟囊性畸胎瘤的重要性。我们介绍了一名 10 岁女性患者的病例,她出现持续性胸痛和呼吸困难。包括胸部 X 光片和对比增强胸部 CT 扫描在内的影像学检查显示,患者前纵隔有一个巨大的、圆形的、伴有钙化的肿块。患者接受了右侧开胸手术,切除了一个 6 × 5 × 5 厘米的成熟囊性畸胎瘤。组织病理学检查证实了诊断结果。患者恢复顺利,病情稳定后出院。纵隔成熟囊性畸胎瘤因其非特异性症状和异质性影像学特征,给诊断带来了挑战。鉴别诊断包括其他含有脂肪和钙化物的纵隔肿块。手术切除是首选的治疗方法,但由于与邻近结构粘连,完全切除可能具有挑战性。有必要进行密切随访,以监测复发和并发症。纵隔成熟囊性畸胎瘤是一种罕见肿瘤,临床表现各异。早期发现和手术干预对获得最佳治疗效果至关重要。这类肿瘤应列入儿科纵隔肿块的鉴别诊断清单。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
165
审稿时长
12 weeks
期刊介绍: The AFMR is committed to enhancing the training and career development of our members and to furthering its mission to facilitate the conduct of research to improve medical care. Case reports represent an important avenue for trainees (interns, residents, and fellows) and early-stage faculty to demonstrate productive, scholarly activity.
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