Konjenital pelvik arteriovenöz malformasyona bağlı spontan masif hematüri
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Dosyalar
Tarih
2014
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
İnönü Üniversitesi Tıp Fakültesi Dergisi
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
Konjenital pelvik arteriyovenöz malformasyon nadir görülen bir hastalık olup genellikle asemptomatiktir. Pelvik arteriyovenöz malformasyonlar sıklıkla tümörlere, pelvik travmaya veya cerrahi işlemlere sekonder akkiz lezyonlardır. Bu makalede konjenital pelvik arteriyovenöz malformasyon nedeniyle spontan masif hematüri gelişen 72 yaşındaki bir bayan hastayı sunuyoruz. Başvuru anında hastanın hemoglobin ve hematokrit değerleri sırasıyla 7.2 g/dL ve %22’ye kadar düşmüştü. Öncelikle hastaya kan replasmanı yapıldı ve mesanedeki hematom boşaltılıp sistoskopik değerlendirmeye gidildi. Sistoskopide mesane tabanında yer yer eritemli alanlar ve pulsasyon şeklinde bir hareketlilik gözlendi. Bunun ardından çekilen bilgisayarlı tomografide pelvik kavitede vasküler malformasyonlar halinde lezyonlar tespit edilen hastanın kesin tanı ve tedavisi anjiografik olarak yapılmıştır.
Congenital pelvic arteriovenous malformation is a rare disease that is usually asymptomatic. Pelvic arteriovenous malformations are often acquired lesions secondary to neoplasms, pelvic trauma or surgical procedures. In this paper, we present a case of spontaneous massive hematuria due to congenital pelvic arteriovenous malformation in a 72-year-old woman. At the time of admission, the patient's hemoglobin and hematocrit values had fallen to 7.2 g/dL and 22%, respectively. First, blood transfusion was done and cystoscopic evaluation was performed after hematoma in bladder was drained. At the cystoscopy, a pulsatile movement and erythematous areas were observed in the base of the bladder. Subsequently, vascular lesions in the pelvic cavity were detected by computed tomography and angiography was performed for definitive diagnosis and treatment of the patient.
Congenital pelvic arteriovenous malformation is a rare disease that is usually asymptomatic. Pelvic arteriovenous malformations are often acquired lesions secondary to neoplasms, pelvic trauma or surgical procedures. In this paper, we present a case of spontaneous massive hematuria due to congenital pelvic arteriovenous malformation in a 72-year-old woman. At the time of admission, the patient's hemoglobin and hematocrit values had fallen to 7.2 g/dL and 22%, respectively. First, blood transfusion was done and cystoscopic evaluation was performed after hematoma in bladder was drained. At the cystoscopy, a pulsatile movement and erythematous areas were observed in the base of the bladder. Subsequently, vascular lesions in the pelvic cavity were detected by computed tomography and angiography was performed for definitive diagnosis and treatment of the patient.
Açıklama
[Turgut Özal Tıp Merkezi Dergisi, (2014).21 (1)]
Anahtar Kelimeler
Arteriovenöz Malformasyonlar, Hematüri, Mesane, Arteriovenous Malformations, Hematuria, Urinary Bladder
Kaynak
Turgut Özal Tıp Merkezi Dergisi
WoS Q Değeri
Scopus Q Değeri
Cilt
21
Sayı
1
Künye
Aktaş, B.Kağan., Özden, C.,Baykam, M. Murat.,Salar, R.,Karabakan, M.,Dede, D.,Memiş, A.,(2014).Konjenital pelvik arteriovenöz malformasyona bağlı spontan masif hematüri.Turgut Özal Tıp Merkezi Dergisi, 21 (1).74-76 ss.
