Abstract
Objectives: Granulosa cell tumors (GCTs) are rare ovarian
neoplasms accounting for approximately 3% of all ovarian
malignancies. They are the most commonmalignant sex cord stromal
tumor. The differences between the two types (juvenile and adult)
are mainly microscopic. GCT is a slow-growing tumor that tends to
recur very late. According to textbooks GCT is a large tumor with
a smooth or lobulated surface with necrotic or hemorrhagic areas.
The majority of the masses are solid; the minority are partially or
totally cystic. Little is known about the correlation with preoperative
sonographic features and most studies only report on the locularity.
The aim of the study was to describe the sonographic features of
the GCT.
Methods: Patients with a GCT that were preoperatively scanned by
a strict protocol were retrospectively included in this analysis.
Results: Nineteen patients were included, three with a juvenile- and
16 with an adult-type GCT. Most GCTs were multilocular solid
(11/19 (58%)) or solid (7/19 (37%)); one mass was unilocular solid.
Some 58% (11/19) of the masses had more than five locules, and
37% (7/19) more than 10 locules. The masses were large with a
mean largest diameter of 116 (37 242) mm. Only three tumors had
papillary projections. All tumors showed increased vascularization;
95% (18/19) had a color score ≥3. The mean PI was 0.69 (0.7 1.8),
the mean RI 0.46 (0.49 0.93) and the mean PSV 21.79 (4 52).
Endometrial pathology was suspected only once on ultrasound but
found in six of the 11 (54.6%) biopsies. The free fluid was suggestive
of a hematoperitoneum in one case and ascites in four cases. In 12/15
masses the subjective impression of the sonologist was a malignant
or a germ cell tumor.
Lingua originale | English |
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pagine (da-a) | 430-431 |
Numero di pagine | 2 |
Rivista | ULTRASOUND IN OBSTETRICS & GYNECOLOGY |
Stato di pubblicazione | Pubblicato - 2007 |
Evento | 17th World Congress on Ultrasound
in Obstetrics and Gynecology - Firenze Durata: 7 ott 2007 → 11 ott 2007 |
Keywords
- granulosa cell tumor