Case Report of a Rare Cystic Mediastinal Lymphangioma Mimicking Recurrent Pleural Effusion.

Case Reports in Radiology Pub Date : 2019-05-26 eCollection Date: 2019-01-01 DOI:10.1155/2019/1301845
Fateme Salehi, Mark Landis, Richard Inculet, Daniele Wiseman
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引用次数: 2

Abstract

Mediastinal lymphangiomas are rare benign congenital malformations, but complications can occur, including infection, cystic hemorrhage, superior vena cava syndrome, airway compromise, and chylothorax. Radiologically, lymphangiomas are well-defined masses, with low attenuation ranging from simple to complex fluid and fat. They often encase adjacent mediastinal structures. We present a case of mediastinal lymphangioma in a young female, who presented with recurrent complex pleural effusions, initially thought to represent an empyema and/or necrotic mass. Despite surgical chest tube and interventional radiology drainage, fluid reaccumulated. Upon further review, the interventional and thoracic radiologist concurred that the complex collection was in fact predominantly extra pleural in location. The patient underwent partial resection after it was discovered intraoperatively that the extra pleural cystic mass was contiguous with and extended deeply into the mediastinum. Histopathology confirmed the diagnosis of lymphangioma.

Abstract Image

罕见的囊性纵隔淋巴管瘤表现为复发性胸腔积液1例报告。
纵隔淋巴管瘤是罕见的先天性良性畸形,但可发生并发症,包括感染、囊性出血、上腔静脉综合征、气道损害和乳糜胸。放射学上,淋巴管瘤是明确的肿块,低衰减,从简单到复杂的液体和脂肪。它们常包住邻近的纵隔结构。我们报告一个年轻女性纵隔淋巴管瘤的病例,她表现为复发性复杂胸腔积液,最初被认为是脓胸和/或坏死肿块。尽管手术胸管和介入放射学引流,液体再次积聚。经过进一步检查,介入和胸椎放射科医生一致认为,复杂的集合实际上主要位于胸膜外。患者术中发现胸膜外囊性肿块与纵隔相邻并深入纵隔,遂行部分切除。组织病理学证实淋巴管瘤的诊断。
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