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Browsing by Author "Milenković, Vera (13006375400)"

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    Publication
    Clinical outcome of a FIGO stage IV gestational choriocarcinoma
    (2013)
    Milenković, Vera (13006375400)
    ;
    Lazović, Biljana (36647776000)
    ;
    MačVanski, Marija (36092923400)
    ;
    Jeremić, Katarina (6701486495)
    ;
    Hrgović, Zlatko (7003671220)
    Choriocarcinoma is the most malignant tumor of gestational trophoblastic disease arising from any gestation. It has a tendency toward relapse as well as metastasis. Here, a case of relapsed high-risk choriocarcinoma (FIGO stage IV, WHO score 12) in a 37-year-old female presenting with vaginal bleedings is described. Relapse developed at the site of the surgical scar from hysterectomy that had been performed 2 years earlier. Although the patient was treated with aggressive chemotherapy, she was in a bad general condition and died from infection and liver insufficiency. © 2013 S. Karger AG, Basel.
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    Publication
    Hypersensitivity to etoposide in case of metastatic gestational choriocarcinoma
    (2013)
    Lazović, Biljana (36647776000)
    ;
    Milenković, Vera (13006375400)
    ;
    Cross D Signelić, Marina (56013943200)
    ;
    Mazić, Sanja (6508115084)
    ;
    Jeremic, Katarina (6701486495)
    ;
    Hrgović, Zlatko (7003671220)
    Etoposide is commonly used in the treatment of a variety of neoplasms. Hypersensitivity reactions to etoposide are infrequently reported and include hypotension, hypertension, flushing, diaphoresis, chest discomfort, dyspnea, bronchospasm and loss of consciousness. We report the case of a 39-year-old woman who experienced acute bronchospasm, tachycardia, hypoxia and hypotension. The symptoms resolved within an hour after administration of intravenous fluids, methylprednisolone, diphenhydramine and oxygen. Subsequently, the patient was given etoposide phosphate without incident. © 2013 S. Karger AG, Basel.
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    Publication
    Term pregnancy after minimally invasive surgical treatment of Herlyn-Werner-Wunderlich syndrome
    (2013)
    Mirković, Ljiljana (23474551800)
    ;
    Ljubić, Aleksandar (6701387628)
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    Janjić, Tijana (56362345500)
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    Milićević, Srboljub (22941572700)
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    Sparić, Radmila (23487159800)
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    Jeremić, Katarina (6701486495)
    ;
    Pantović, Sveto (55340482900)
    ;
    Milenković, Vera (13006375400)
    Introduction Uterus didelphys with obstructed hemivagina and ipsilateral renal agenesis represents a complex congenital anomaly, also known in the literature as Herlyn-Werner-Wunderlich (HWW) syndrome. Case Outline A 16-year-old patient presented with secondary amenorrhoea and abdominal pain. Her history revealed anorexia nervosa; she had menarche at the age of 14; her menstrual cycles were regular, with progressive dysmenorrhoea. Nine months after the explorative laparotomy performed at the regional healthcare center there was no a definitive diagnosis. Pelvic examination showed a paravaginal pelvic mass located on the right side. Magnetic resonance imaging of the abdomen and pelvis confirmed the diagnosis of HWW syndrome. Transvaginal excision and marsupialisation of the vaginal septum were performed. Regular menstrual cycles were resumed after four years following the treatment of anorexia nervosa. Twelve years after the operation, the patient conceived spontaneously; pregnancy developed in the left non-obstructed uterus. She underwent Cesarean section at the 37th gestational week and gave birth to a healthy female infant. Conclusion HWW syndrome is an uncommon cause of abdominal pain and progressive menstrual discomfort shortly after menarche. It is therefore essential to maintain a high index of suspicion of the existence of this syndrome in such cases, since prompt and adequate treatment prevents the development of complications and allows for preservation of the reproductive potential of both hemi-uteri.

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