Malignant Germ cell Tumor of Ovary: An Unusual Combination and An Irony of Fate

نویسندگان

چکیده

Malignant mixed ovarian germ cell tumors are very rare malignant tumors, with a high degree of malignancy. They aggressive cancers affecting young adolescent girls. The commonest combination reported in literature is dysgerminoma and endodermal sinus tumors. Fertility sparing surgery followed by chemotherapy the treatment choice. objectives this case report advanced age presentation, unusual histopathological combination, irony infertility treatment. We 40-year-old woman tumor comprising components tumor, immature teratoma, embryonal carcinoma. Patient was on hormonal therapy for cause infertility, presented complains lower abdominal pain, constipation incomplete evacuation bladder 2months. Transvaginal ultrasonography CT scan showed large multicystic space occupying lesion predominant solid component midline abdominopelvic location. Tumor markers i.e., AFP, Prolactin CA125 were raised. Total hysterectomy bilateral salpingoophorectomy, pelvic retroperitoneal node resection, peritonectomy omentectomy performed.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Malignant mixed germ cell tumour of ovary- an unusual combination and review of literature

Mixed germ cell tumours of the ovary are malignant neoplasms of the ovary comprising of two or more types of germ cell components. Most of the malignant mixed germ cell tumours consists of dysgerminoma accompanied by endodermal sinus tumours, immature teratoma or choriocarcinoma. There are only few case reports of mixed germ cell tumours with different combinations of malignant components. We r...

متن کامل

development and implementation of an optimized control strategy for induction machine in an electric vehicle

in the area of automotive engineering there is a tendency to more electrification of power train. in this work control of an induction machine for the application of electric vehicle is investigated. through the changing operating point of the machine, adapting the rotor magnetization current seems to be useful to increase the machines efficiency. in the literature there are many approaches wh...

15 صفحه اول

Secondary Malignant Transformation of Giant Cell Tumor of Bone: Is It a Fate?

The malignant transformation of conventional giant cell tumor of bone (GCTOB) is rare and usually occurs with irradiation. Here we report two neglected cases of conventional GCTOB with spontaneous malignant transformation at 11 and 16 years after initial diagnosis. In the former case, the patient refused to receive any treatment following the incisional biopsy, and in the latter, the firs...

متن کامل

AN UNUSUAL PRESENTATION OF EXTRARENAL MALIGNANT RHABDOID TUMOR OF SOFT TISSUE: A CASE REPORT AND REVIEW OF THE LITERATURE

Extra renal extra cranial malignant rhobdoid tumors (MRT) are rare, frequently lethal and affect mostly children. No definite treatment has been made and the role of radiation therapy is poorly defined. This report explains a 14 year old girl with MRT in her neck soft tissue. She is alive with no evidence of disease 18 months after diagnosis. Through the experience with this case, we suggested...

متن کامل

ovarian malignant mixed germ cell tumor: a case of unusual presentation as molar pregnancy

background: this research was conducted to introduce a patient with rare ovarian mixed germ cell tumor, presented as molar pregnancy. case presentation: the patient was a 16 year old woman admitted with diagnosis of molar pregnancy. abdominal enlargement was the only complaint. she had a large pelvic mass in physical examination. the first diagnosis was molar pregnancy due to previous ultrasoni...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Annals of Pathology and Laboratory Medicine

سال: 2021

ISSN: ['2349-6983', '2394-6466']

DOI: https://doi.org/10.21276/apalm.3080