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dysgerminoma/abdominal pain

הקישור נשמר בלוח
מאמריםניסויים קלינייםפטנטים
עמוד 1 מ 47 תוצאות

Advanced ovarian dysgerminoma infiltrating both ovaries and uterus in a 7-year-old girl.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Introduction. Ovarian dysgerminoma is a rare malignant ovarian germ cell tumor with its peak incidence in young women. Abdominal pain, abdominal distention, and the presence of a palpable mass are common symptoms at presentation. Depending on the FIGO stage at presentation the prognosis of

Surgical resection of a dysgerminoma in a mare.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
A mare was referred for further evaluation of a mass found in the left caudal abdomen during a routine postpartum reproductive palpation. The mare was clinically normal with no history of health problems. Ultrasonographic examination of the mass confirmed its presence, but the origin of the mass

Torsion of Ovarian Dysgerminoma in a Child: Role of Computed Tomography.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Dysgerminomas are malignant germ cell tumors of the ovary that most commonly occur in the adolescent population. Ovarian dysgerminoma presenting with complications like torsion is a rare entity in the pediatric age group. Cross-sectional imaging plays a crucial role in diagnosis, tumor staging

[Clinical analysis of 57 patients with ovarian dysgerminoma].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
OBJECTIVE Ovarian dysgerminoma is an uncommen ovarian malignancy. Its clinical features are special and there are many factors influencing the prognosis. If treated properly, the patient can be cured. Otherwise it may endanger the patient's life. The aim of this study is to investigate the clinical

[Antierythrocyte antibodies due to ovarian dysgerminoma. A case report].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
The case of a 24-year-old woman with fever, abdominal pain and weight loss, is presented. Right ovarian dysgerminoma was diagnosed; group A blood, negative direct Coombs. The search for free serum antibodies was positive, with specificity: auto anti 1, anti P with activity at 37 degrees C.

[A case of PEP(BEP)-resistant ovarian dysgerminoma successfully treated by VeIP therapy].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Ovarian germ cell tumors are malignant tumors which commonly develop during childhood, and which are sensitive to chemotherapy. We have had a case of germ cell tumors which showed resistance to first-line PEP(BEP)chemotherapy. As second-line chemotherapy, VeIP therapy was used, because it is

Bilateral Gonadoblastoma With Dysgerminoma in a Phenotypically Normal Female With 46XX Karyotype: Report of a Rare Case and Literature Review

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Gonadoblastoma is a rare ovarian neoplasm which belongs to "germ cell-sex cord-stromal tumor" category. This tumor is frequently associated with invasive germ cell malignancy. It commonly arises in dysgenetic gonads of young individuals who are phenotypically females but possess 46XY karyotype. It

Internal hemorrhage caused by a twisted malignant ovarian dysgerminoma: ultrasonographic findings of a rare case and review of the literature.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
OBJECTIVE Ovarian cancer presents as an acute abdomen very rarely. The purpose of the study is the description of a right ovarian malignant dysgerminoma presenting as an abdominal emergency. METHODS A 16-year-old white female presented with acute abdominal pain in the right iliac fossa. On physical

[An ovarian tumor with structural gonadoblastoma, dysgerminoma and choriocarcinoma].

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
A 14 1/2-year old girl with menometrorrhagia followed by amenorrhea and abdominal pain had a pelvic resistance with limited mobility. Histology of a left ovarian tumour showed gonadoblastoma turning to dysgerminoma and associated with choriocarcinoma (M-9073/1, M-9060/3, M-90101/3). Genuine ovarian

Ovarian dysgerminoma in an adolescent: a case report.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
BACKGROUND Ovarian cancer is the second most frequent gynaecological cancer in Nigeria ranking next after carcinoma of the cervix. It has the highest case-fatality rate worldwide because of insidious onset, lack of effective screening methods and late presentation. This case of a sixteen-year old

Ovarian dysgerminoma and acute abdomen.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
BACKGROUND Ovarian dysgerminoma cases are very rarely presented together with acute abdomen. The purpose of this study is to present dysgerminoma ovarii with abdominal pain in lower right abdominal part after abdominal trauma as an abdominal emergency. METHODS Our 12-year old female patient was

Imaging Findings in Dysgerminoma in a Case of 46 XY, Complete Gonadal Dysgenesis (Swyer syndrome).

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
A 46 XY pure gonadal dysgenesis also known as Swyer syndrome. These patients are phenotypic females with normal female external genitalia and absent testicular tissue. The patients with swyer syndrome have streak gonads and increased risk of dysgerminoma and gonadoblastoma. We present a case of

Paraneoplastic Cholestasis Associated With Ovarian Dysgerminoma.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
BACKGROUND Paraneoplastic syndromes are disorders caused by cancer that are not a direct result of the cancer mass itself or metastases to the affected organ. Paraneoplastic cholestasis is described with lymphoma and renal cell carcinoma. Unlike ovarian carcinoma, paraneoplastic syndromes are rarely

Ovarian dysgerminoma with normal serum tumour markers presenting in a child with precocious puberty.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
A 7-year-old female child was presented to the emergency room with acute abdominal pain and vaginal bleeding. Her assessment revealed a firm large lower abdominal mass with evidence of precocious puberty with bilaterally symmetrically enlarged breast (Tanner stage B4-P1-A1). Abdominal imaging showed

Fine needle aspiration diagnosis of bilateral dysgerminoma with syncytiotrophoblastic giant cells.

רק משתמשים רשומים יכולים לתרגם מאמרים
התחבר הרשם
Dysgerminoma accounts for only 1-3% of ovarian cancers and about 30-40% of all ovarian germ cell malignant tumors. Literature states that about 2% of nonpregnant patients with dysgerminomas present with elevated serum or urine levels of human chorionic gonadotropin (hCG). Here, we report a 34
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