𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Lymphatic and venous malformation or “lymphangiohemangioma“ of the anterior mediastinum: case report and literature review

✍ Scribed by Yoshihisa Kadota; Tomoki Utsumi; Tomohiro Kawamura; Masayoshi Inoue; Noriyoshi Sawabata; Masato Minami; Meinoshin Okumura


Publisher
Springer Japan
Year
2011
Tongue
Japanese
Weight
362 KB
Volume
59
Category
Article
ISSN
1863-6705

No coin nor oath required. For personal study only.

✦ Synopsis


Lymphatic and venous malformations (LVM) are tumor-like lesions combining dysplastic lymphatic and venous vessel structures. They are rarely found in the mediastinum. We present a case of mediastinal LVM, with review of the literature. An asymptomatic 60-yearold man presented for evaluation of an anterior mediastinal mass. On chest computed tomography (CT), the mass demonstrated contrast enhancement and its 7-mm vein draining directly into the left brachiocephalic vein. The tumor was resected completely using video-assisted thoracoscopic surgery. The surgical specimen revealed combined features of venous and lymphatic dysplasia, and was diagnosed it as LVM, so-called mediastinal lymphangiohemangioma. Management plans based on precise imaging studies using magnetic resonance imaging and multi-detector-row CT phlebography could be helpful in guiding both preoperative diagnosis and subsequent treatment decisions for mediastinal LVM.


📜 SIMILAR VOLUMES


Arteriovenous malformation of the base o
✍ Paul D. Righi; Maseer A. Bade; John J. Coleman III; Melissa Allen 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 230 KB 👁 1 views

Arteriovenous malformations of the head and neck pose a challenging therapeutic and reconstructive problem. In this report we describe a rare case of an arteriovenous malformation of the base of tongue. The patient, a young adult female, was treated with embolization followed by surgical resection u

Malignant paraganglioma of the posterior
✍ Robert Odze; Louis R. Bégin 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 732 KB

A case of malignant paraganglioma arising from the posterior mediastinum and presenting with a chest wall metastasis is reported with immunocytochemical and ultrastructural documentation. The pathobiologic features of this rare disease are reassessed with a review of the literature. Cytoarchitectura