Journals / Jinekoloji Obstetrik Pediatri ve Pediatrik Cerrahi Dergisi / 2012 / Cilt: 4 - Sayı: 2

A rare case of fetal extremity tumor: Hemangiolymphangioma

Ender görülen fetal ekstremite tümörü: Hemanjiolenfanjioma

Pages
89–92
Publication Date
2022-10-18
DOI
—
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AI Summary & Key Takeaways

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

We aimed to present our experience about prenatal diagnosis, perinatal outcome and the treatment in postnatal period of an extremely rare case of HL.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Hemangiolymphangioma (HL) is a rare vascular malformation.
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Key Findings & Data:Thirty-two-year-old woman with 38 weeks of pregnancy was referred to our clinic because of the mass of fetal arm.
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Conclusion & Impact:We aimed to present our experience about prenatal diagnosis, perinatal outcome and the treatment in postnatal period of an extremely rare case of HL.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hemangiolymphangioma (HL) is a rare vascular malformation. Thirty-two-year-old woman with 38 weeks of pregnancy was referred to our clinic because of the mass of fetal arm. Ultrasonography revealed the large mass which believed to be HL with solid and cystic components in the fetal right upper extremity. In postnatal period, doppler ultrasonography (USG) and Magnetic Resonance Imaging (MRI) tests found the mass to be compatible with HL. Excisional biopsy is not recommended after pediatri, pediatric surgery and orthopedic consultations. In the neonatal period, the propranolol treatment was started because of component of hemangiomas in the mass. The continue treatment with propranolol was decided on the reduction of mass size after the third month. We aimed to present our experience about prenatal diagnosis, perinatal outcome and the treatment in postnatal period of an extremely rare case of HL.

Özet

Hemanjiolenfanjioma (HL) oldukça ender görülen vasküler malformasyondur. Otuz iki yaşında 38 haftalık gebeliği olan kadın hasta fetal kolda kitle nedeniyle polikliniğimize refere edildi. Yapılan ultrasonografide, fetal sağ üst ekstremitede solid ve kistik komponentleri bulunan ve ön tanı olarak HL olduğu düşünülen kitle saptandı. Postnatal yapılan doppler ultrasonografi (USG) ve Manyetik Rezonans Görüntüleme (MR) tetkiklerinde kitlenin HL ile uyumlu olduğu saptandı. Çocuk hastalıkları, çocuk cerrahisi ve ortopedi konsültasyonları sonrasında eksizyonel biopsi önerilmedi. Neonatal dönemde hemanjiom komponenti nedeniyle propranolol tedavisi başlanıldı. Propranolol ile tedavinin üçüncü ayında kitle boyutlarında küçülme saptanması üzerine bu tedavinin devamına karar verildi. Prenatal dönemde tanısı konulan ve oldukça ender rastlanan HL olgusuna ait prenatal tanı, perinatal sonuç ve postnatal dönemde tedavisi ile ilgili deneyimimizi sunmayı amaçladık.

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Cite This Article

EVSEN, M. S., SOYDİNÇ, H. E., VURAL, S., TANER, M. Z., SAK, M. E., ÖZLER, A. (2022). A rare case of fetal extremity tumor: Hemangiolymphangioma. Jinekoloji Obstetrik Pediatri ve Pediatrik Cerrahi Dergisi, Cilt: 4 - Sayı: 2, 89–92. https://ajindex.com/articles/558548

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