| Autor: |
Joshi, R., Baral, G., Malla, K. |
| Předmět: |
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| Zdroj: |
Nepal Journal of Obstetrics & Gynaecology; Jan-Jun2018, Vol. 13 Issue 1, p57-60, 4p |
| Abstrakt: |
Introduction: Adult granulosa cell tumor is a rare tumor which accounts for 1% of all ovarian tumors. They usually present with postmenopausal bleeding and abdominal mass. Inhibin is used as the tumor marker. Case: A 76 years multiparous post-menopausal women presented with vaginal bleeding for past three years and painless huge mass in lower abdomen. She underwent total abdominal hysterectomy with bilateral salphingo-oophorectomy with bilateral pelvic lymphnode dissection with appendectomy. Histopathology showed the adult granulosa cell tumor with few mitosis, Stage IA. Her postoperative period was uneventful. Conclusion: Surgery is the mainstay of treatment of granulosa cell tumor and chemotherapy is indicated in advanced cases. Although they have better prognosis, life-long follow up is advised to detect late recurrence. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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