Gebelik s�ras�nda nadir g�r�len bir t�m�r; juvenil gran�losa h�creli t�m�r

Temizkan, Osman; A�ar, Sema; Kabil Kucur, Suna; Ba�aran, Toygun; Temizkan, �ule; A��c�o�lu, Osman

Cilt : 58 Say� : 1 Y�l : 2024

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Gebelik s�ras�nda nadir g�r�len bir t�m�r; juvenil gran�losa h�creli t�m�r [Med Bull Sisli Etfal Hosp]

Med Bull Sisli Etfal Hosp. 2013; 47(4): 212-215 | DOI: 10.5350/SEMB2013470410

Gebelik s�ras�nda nadir g�r�len bir t�m�r; juvenil gran�losa h�creli t�m�r

Osman Temizkan¹, Sema A�ar¹, Suna Kabil Kucur¹, Toygun Ba�aran¹, �ule Temizkan², Osman A��c�o�lu²
¹�i�li Etfal E�itim ve Ara�t�rma Hastanesi, Kad�n Hastal�klar� ve Do�um Klini�i, �stanbul
²Kartal E�itim ve Ara�t�rma Hastanesi, Endokrinoloji Ve Metabolizma Hastal�klar� Klini�i, �stanbul

J�venil granuloza h�creli t�m�rler (JGHT) overin malign seks kord stromal t�m�rlerindendir. Granuloza h�creli t�m�rlerin sadece %5 kadar�n� olu�turur. Gebelikle birlikte bildirilmi� olduk�a az say�da JGHT olgusu tan�mlanm��t�r. JGHT�de y�ksek mitotik aktivite ve n�kleer atipi nadiren g�r�lse de prognozu �ok iyidir. Biz burada gebelik s�ras�nda 17 cm �ap�nda sa� adneksiyel kitlesi olan ve unilateral salpingooferektomi ile tedavi edilen 20 ya��nda bir j�venil granuloza h�creli t�m�r olgusunu inceledik ve bu nadir g�r�len vakan�n prognozunu ve takibini literat�r e�li�inde sunmay� ama�lad�k.

Anahtar Kelimeler: J�venil granulosa h�creli t�m�r, over t�m�rleri, gebelik

A rare tumor during pregnancy; juvenile granulosa cell tumor

Osman Temizkan¹, Sema A�ar¹, Suna Kabil Kucur¹, Toygun Ba�aran¹, �ule Temizkan², Osman A��c�o�lu²
¹Department of Obstetrics and Gynecology, �i�li Etfal Training and Research Hospital, �stanbul, Turkey
²Department of Endocrinology and Metabolic Diseases Kartal Training and Research Hospital, �stanbul, Turkey

Juvenile Granulosa Cell Tumors (JGCT) are the one of the malignant ovarian tumors of sex cordstromal origin. Only 5% of granulosa cell tumors are JGCT. There are only a few reported cases of JGCT during pregnancy. JGCT has a good prognosis although it has rarely high mitotic activity and nuclear atipy. Here we reported a case JGCT case with JGCT diagnosed during pregnancy. She was 20-yearold and had a mass in the right adnexial region 17 cm in size. She was performed unilateral salphingoopherectomy. We discussed the prognosis and follow-up of this rare phenomenon in the contrast of the literature.

Keywords: Juvenile granulosa cell tumors, ovarian tumors, pregnangy

Osman Temizkan, Sema A�ar, Suna Kabil Kucur, Toygun Ba�aran, �ule Temizkan, Osman A��c�o�lu. A rare tumor during pregnancy; juvenile granulosa cell tumor. Med Bull Sisli Etfal Hosp. 2013; 47(4): 212-215

Sorumlu Yazar: Osman Temizkan, T�rkiye
Makale Dili: T�rk�e

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