Browsing by Author "Erdemoglu, E."

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Giant Bladder Leiomyoma Presenting as a Pelvic Mass: a Case Report
(I R O G Canada, inc, 2007) Erdemoglu, E.; Kamaci, M.
We present a rare case of bladder leiomyoma with an unusual presentation as a pelvic mass. Bladder leiomyomas are very rare tumors, compromising less than 0.43% of all bladder tumors. Magnetic resonance imaging showed a 16 x 13 cm mass covering the entire pelvis and extending up to the umbilicus. There was a 20 x 20 x I I cm immobile mass originating from the bladder at laparotomy. The mass was removed by bladder-sparing surgery and was reported to be leiomyoma. We conclude that bladder leiomyomas should be preoperatively recognized as a cause of pelvic mass in order to make the possible diagnosis.
Ovarian Gonodoblastoma With Yolk Sac Tumor in a Young 46, Xx Female: Case Report
(I R O G Canada, inc, 2007) Erdemoglu, E.; Ozen, S.
Background: Gonodoblastomas with ovarian germ cell tumors (OGCTs) other than dysgerminoma are very unusual. This is the first case report of a pure endodermal sinus tumor of the ovary with gonodoblastoma in a 46 XX, female. Case: A 19-year-old female was admitted to our hospital with an abdominal mass and pain. She had elevated levels of CA-125 and AFP Fertility sparing surgery was undertaken and revealed a Stage IA endodermal sinus tumor and gonodoblastoma in the same ovary. The patient refused chemotherapy and was followed-up for six months without disease. Conclusion: Gonodoblastomas may occur in conjunction with OGCTs. Tumor markers and immunohistochemical examination may help in the diagnosis of these OGCTs with gonodoblastoma.
Prenatal Diagnosis of Urethropelvic Obstruction and Assesment of Fetal Renal Function: Case Report
(2006) Erdemoglu, E.; Kolusari, A.; Şahin, H.G.; Kamaci, M.
Fetal obstructive renal anomalies ar the most common urinary anomaly. Obstuction is particularly is encountered in ureteropelvic junction, vesicoureteral juction or urethra. Accurate localisation of obstruction and status of fetal kidneys are of utmost importance in prognosis and intrauterin management. Thirtythree years old, G6P5A0 women at 20th gestational weeks was refered for anhidroamnios and urinary to deparment of Obstetrics and Gynecology, Yuzüncü Yil Univeristy Medical Faculty. B-mod ultrasonographic examination was likely a posterior urethral valve however, color doppler and pulse doppler examination revealed obstruction cranial to fetal bladder. Pyelourethrocenetsis to evaluate renal function and amnioinfusion was performed. Right renal cortex was thin and hiperechogenic, collecting tubules were dilated. Collecting tubules of right kidney was minimally dilated. Biochemical analysis of aspirated fluid and anhidroamniosis gave irreversible renal damage and pregnancy was terminated. There was left renal duplication and right grade 4 hydronephrosis due to ureteopelvic obstruction. Bladder and urethra was normal. Color doppler and pulse doppler examiation should be incorporated to B-mod examination to assess localisation of urinary obstruction. Uretherocentesis and amniotic fluid index should be examined in order to evaluate prognosis of fetal kidneys.
Primary Giant Leiomyoma of the Ovary -: Case Report
(I R O G Canada, inc, 2006) Erdemoglu, E.; Kamaci, M.; Bayram, I.; Guler, A.; Guler Sahin, H.
Primary leiomyoma of the ovary, which is of unknown origin, is an extremely rare tumor of ovary. We report a rare case of giant primary ovarian leiomyoma with an unusual presentation, ascites, elevated CA125 and discuss the preoperative imaging findings. A 45-year-old woman was referred for evaluation of an adnexal mass of 8 x 9 cm with ascites and elevated CA125 levels. Preoperative imaging studies were in accordance with fibroma/thecoma. At laparotomy total abdominal hysterectomy and bilateral salpingo-oophorectomy were performed. Histological and immunhistochemical examination revealed primary ovarian leiomyoma.