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Journals / Abant Tıp Dergisi / 2015 / Cilt: 4 Sayı: 4

An intracranial hemorrhage in a patient with Klippel-Trenaunay syndrome and Hemophilia B association

İntrakraniyal kanamalı bir olguda Klippel-Trenaunay sendromu ve Hemofili B birlikteliği

Zühal Örnek(Bülent Ecevit Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Zonguldak)
İbrahim Etem Pişkin(Bülent Ecevit Üniversitesi Tıp Fakültesi, Çocuk Sağlığı ve Hastalıkları Anabilim Dalı, Zonguldak)
Mehmet Karacı(Beykoz Devlet Hastanesi, Çocuk Sağlığı Ve Hastalıkları Kliniği, İstanbul.)
Pages
387–390
Publication Date
2015-11-01
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

We report a case that KTS in a patient presented with intracranial hemorrhage was bound to hemophilia B.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Klippel-Trenaunay syndrome KTS , a rare congenital disorder, is characterized by cutaneous vascular malformation, soft tissue-bony hypertrophy and varicose veins.
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Key Findings & Data:KTS does not only show peripheral involvement, but also visceral involvement may be observed which is an important source of morbidity and mortality.
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Conclusion & Impact:We report a case that KTS in a patient presented with intracranial hemorrhage was bound to hemophilia B.
🔬Design:Makale
📍Scope:Comprehensive Sample
⚙️Variables:Klippel-Trenaunay sendromu · Hemofili B · intrakranial kanama

Abstract

Klippel-Trenaunay syndrome KTS , a rare congenital disorder, is characterized by cutaneous vascular malformation, soft tissue-bony hypertrophy and varicose veins. KTS does not only show peripheral involvement, but also visceral involvement may be observed which is an important source of morbidity and mortality. Intracranial hemorrhage in KTS is extremely rare and usually traced to an underlying arteriovenous malformation or fistula. We report a case that KTS in a patient presented with intracranial hemorrhage was bound to hemophilia B.

Özet

Klippel-Trenaunay Sendromu KTS , kutanöz vasküler malformasyonlar, kemik ve yumuşak doku hipertrofisi ve variköz venler ile karakterize ender konjenital bir sendromdur. KTS’de hem periferik hem de visseral tutulum gözlenebilir ve bu önemli morbidite ve mortalite kaynağı olabilir. KTS de intrakranial kanamaya oldukça nadir rastlanır ve altında genellikle arteriovenöz malformasyonlar veya fistül mevcuttur. Bu olgu KTS’lu bir hastadaki intrakranial kanamanın sebebinin Hemofili B olması nedeniyle sunulmuşur.

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Cite This Article

Örnek, Z., Pişkin, İ. E., Karacı, M. (2015). An intracranial hemorrhage in a patient with Klippel-Trenaunay syndrome and Hemophilia B association. Abant Tıp Dergisi, Cilt: 4 Sayı: 4, 387–390. https://doi.org/10.5505/abantmedj.2015.50023

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