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Primary intrathymic lymphangioma in an infant


1 Division of Cardiothoracic and Vascular Surgery, Sri Sathya Sai Institute of Higher Medical Sciences Whitefield, Bengaluru, Karnataka, India
2 Department of Anaesthesiology, Sri Sathya Sai Institute of Higher Medical Sciences Whitefield, Bengaluru, Karnataka, India

Correspondence Address:
Dr. Channabasavaraj S Hiremath
Department of CTVS, Sri Sathya Sai Institute of Higher Medical Sciences, Whitefield, Bengaluru - 560 066, Karnataka
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_92_19

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Year : 2020  |  Volume : 13  |  Issue : 2  |  Page : 160-162

 

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Lymphangiomas are relatively uncommon lesions of the lymphatic channels which can arise in virtually any part of the body. Although the most common site is the head/neck region, they could be found in the mediastinum. If mediastinal lymphangiomas are said to be rare, the thymic subentity is even scanty. We describe one case of mediastinal lymphangioma with a true intrathymic localization, which to our knowledge has been reported just once in the literature. This case report elucidates the surgical management of the first lymphangioma reported in an infant.






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1 Division of Cardiothoracic and Vascular Surgery, Sri Sathya Sai Institute of Higher Medical Sciences Whitefield, Bengaluru, Karnataka, India
2 Department of Anaesthesiology, Sri Sathya Sai Institute of Higher Medical Sciences Whitefield, Bengaluru, Karnataka, India

Correspondence Address:
Dr. Channabasavaraj S Hiremath
Department of CTVS, Sri Sathya Sai Institute of Higher Medical Sciences, Whitefield, Bengaluru - 560 066, Karnataka
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apc.APC_92_19

Rights and Permissions

Lymphangiomas are relatively uncommon lesions of the lymphatic channels which can arise in virtually any part of the body. Although the most common site is the head/neck region, they could be found in the mediastinum. If mediastinal lymphangiomas are said to be rare, the thymic subentity is even scanty. We describe one case of mediastinal lymphangioma with a true intrathymic localization, which to our knowledge has been reported just once in the literature. This case report elucidates the surgical management of the first lymphangioma reported in an infant.






[FULL TEXT] [PDF]*


        
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