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Subject: hemoglobin
Subject: red blood cells
Subject: Hematocrit
Subject: Granulosa Cell Tumors
Subject: Juvenile Granulosa Cell Tumor
Subject: Adult Granulosa Cell Tumor


Year: 2023


Type: Article



Title: Postpartum Juvenile Granulosa Cell Tumor: A Case Report


Author: Antovska, Vesna
Author: Dabeski, Drage
Author: Aleksioska Papestiev, Irena
Author: Pejkovska Ilieva, Maja
Author: Akiku Kamberi, Elmedina
Author: Sozovska Belchovska, Eva
Author: Zdravkovski, Panche



Abstract: Granulosa Cell Tumors (GCTs) are extremely rare, sex cord-stromal tumors constituting only 1% to 2% of all ovarian malignancies. On the basis of age of onset and pathohistological characteristics, these tumors are subdivided into two distinct forms, the adult type (AGCT) and the juvenile type (JGCT), representing 95% and 5% of the tumors, respectively. Compared to the adult type, which is more common in the fifth decade, JGCT is rarely seen and the majority (90%) is reported in prepubertal individuals or those aged less than 30 years. We report an interesting case of a 24-years old woman with enormous ovarian juvenile granulosa cell tumor of the right ovary. Considering all the anamnestic data and ultrasound reports before and during the first pregnancy, where there has been no evidence for the presence of any tumor, we came to conclusion that the tumor grew rapidly during the first year since delivery. Maybe the tumor was present during the pregnancy or even before, but most probably it was not noticed because it small initial size or it was masked by the growing uterus at ultrasound. The first data for the tumor existence is 3 months before the surgical treatment.


Publisher: Austin Publishing Group


Relation: Austin Gynecology Case Reports



Identifier: oai:repository.ukim.mk:20.500.12188/25570
Identifier: http://hdl.handle.net/20.500.12188/25570



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Postpartum Juvenile Granulosa Cell Tumor: A Case Report202336