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    Poland’s Syndrome
    (Düzce Üniversitesi, 2011) Bulut, İsmet; Kantarcı, Mecit; Koplay, Mustafa
    Poland’s syndrome (PS) is a rarely encountered congenital disorder that is characterised withabsence of pectoralis major muscle. However, hand and other organ anomalies may accompanythe syndrome. It is usually right sided. We report the left sided two PS cases. In diagnosis,physical examination and radiological imaging findings such as chest radiography and computedtomography (CT) are important. Constructive surgery is the prior approach for treatment of thissyndrome. 3 dimension volume rendered imaging features of multidetector CT give importantinformation about determining preopererative radiological details in the PS cases
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    Portal hypertension due to alveolar Echinococcosis and recanalized paraumbilical vein
    (2012) Yılmaz, Ömer; Koplay, Mustafa; Onbaş, Ömer; Aydınlı, Bülent
    Hepatic alveolar echinococcosis is an uncommon parasitic disease caused by Echinococcus multilocularis. It carries high fatality rates and poor prognosis if not diagnosed early and managed correctly. We report a 29-year-old female patient who admitted to our clinic with fatigue, weight loss and abdominal bloating in her right upper quadrant. Physical examination revealed the presence of a large palpable mass in her right upper quadrant, ascites and bilateral pedal edema. Computed tomography revealed a large non-homogeneous mass located in the right lobe of the liver and a dilated paraumbilical vein arising from the left branch of the portal vein. Echinococcus serology assessed by enzyme-linked immunosorbent assay was noted to be positive. Histopathologic examination of the hepatic mass was consistent with alveolar echinococcosis. The patient's complaints were determined as being related to cirrhosis due to alveolar echinococcosis. Alveolar echinococcosis must be considered in patients with portal hypertension of uncertain etiology, especially in endemic regions.
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    Pregnancy in Uterus Didelfis: A Case Report
    (Düzce Üniversitesi, 2009) Sak, M Erdal; Koplay, Mustafa; Özkul, Özgür; Sak, Sibel; Çaça, Fatma Nur
    Uterine abnormalities are rarely seen in pregnant women and may lead to a lot of obstetrics complications. The incidence of Mullerian Duct abnormalities are reported as 0.1-3.8%, however the incidence of uterine didelphis(UD) are estimated 5% between this abnormalities and it is a well-known cause of infertility. In this case report clinical and radiological characteristics of UD and pregnancy co-incidence were evaluated together with literature knowledge
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    Total anomalous pulmonary venous connection draining into the portal vein in a 2-month-old infant: multidetector computed tomography angiography diagnosis
    (Sage Publications Ltd, 2011) Onbaş, Ömer; Koplay, Mustafa; Kandiş, Hayati; Beşir, F.H.; Erdoğmuş, B.
    Total anomalous pulmonary venous connection (TAPVC) is a rare congenital cardiac anomaly in which the pulmonary veins fail to connect with the left atrium and connect directly to the right atrium or to one of the systemic veins. Early diagnosis and surgical correction is highly important for survival. In the evaluation of TAPVC, imaging methods such. as echocardiography, computed tomography (CT) angiography, magnetic resonance (MR) angiography, and catheter angiography have been used. We reported a rare case of infracardiac type of TAPVC draining into the portal vein at 2-mounth-old infant who was admitted to the hospital with shortness of breath and mild cyanosis. The images demonstrating TAPVC between the portal vein and the pulmonary veins with multidetector computed tomography (MDCT) angiography were also shown. (Hong Kong j.emerg.med. 2011;18:331-334)