Juvenile Type Granulosa Cell Tumor

Hormone-producing ovarian tumors in children (a clinical case of managing a patient with a granulosa cell tumor of the juvenile type)

Problemy reproduktsii ◽

10.17116/repro20212705148 ◽

2021 ◽

Vol 27 (5) ◽

pp. 48

Author(s):

L.V. Adamyan ◽

E.V. Sibirskaya ◽

S.A. Korotkova ◽

E.A. Karapetyan ◽

E.I. Polyakova ◽

...

Keyword(s):

Granulosa Cell ◽

Clinical Case ◽

Granulosa Cell Tumor ◽

Cell Tumor ◽

Ovarian Tumors ◽

Juvenile Type

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Juvenile Type Granulosa Cell Tumor

Serbian Journal of Experimental and Clinical Research ◽

10.1515/sjecr-2017-0016 ◽

2018 ◽

Vol 19 (4) ◽

pp. 389-392

Author(s):

Branko Andric ◽

Petar Arsenijevic ◽

Nikola Jovic ◽

Neda Arsenijevic ◽

Zoran Protrka

Keyword(s):

Female Patient ◽

Granulosa Cell ◽

Granulosa Cell Tumor ◽

Cell Tumor ◽

Plasma Testosterone ◽

Histopathological Analysis ◽

Gynecology And Obstetrics ◽

Gynecological Examination ◽

Clinical Center ◽

Juvenile Type

Abstract Granulosa cell tumor is a type of neoplasm, which represents 2-5% of all ovarian cancers. About 5% of these tumors are juvenile- type and usually occur to girls before puberty and to women younger than thirty years of age. There are signs premature puberty or premature emergence of secondary sexual characteristics with irregular vaginal bleeding that occur to these kind of patients. To the rare cases, like this, the occurrence of granulosa cell tumors can cause the appearance of hyperandrogenism with high levels of plasma testosterone, leading to virilization which happened to this female patient. We will present the female patient who was 35 years old and which was originally hospitalized to the Clinic for Haematology Clinical Center Kragujevac, because of extreme fatigue accompanied by dizziness. During diagnostics the patient underwent to the complete gynecological examination. After gynecological examinations and necessary diagnostic procedures, it was decided continuing the treatment at the Clinic of Gynecology and Obstetrics Clinical Center Kragujevac, where she underwent a total abdominal hysterectomy with bilateral salpingo- oophorectomy for suspected uterine neoplasm. Histopathological analysis of the obtained material confirmed the presence of follicular cysts of both ovaries and juvenile type granulosa cell tumor on the right ovary; the uterus was enlarged with multiple fibroid tumors. Granulosa cell tumor should be suspected in the cases of girls and young females if there is present an ovarian cyst paired with signs of preterm puberty or hyperestrogenism. In this case, the presence of granulosa cell tumor was masked by signs of hyperandrogenism, which is not so typical, as well as the presence of uterine fibroids who have actually been the main cause for surgical treatment.

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Adult Type Granulosa Cell Tumor: A Very Rare Case of Sex-Cord Tumor of the Testis with Review of the Literature

Case Reports in Pathology ◽

10.1155/2013/932086 ◽

2013 ◽

Vol 2013 ◽

pp. 1-4 ◽

Cited By ~ 2

Author(s):

Dimosthenis Miliaras ◽

Eleftherios Anagnostou ◽

Ioannis Moysides

Keyword(s):

Granulosa Cell ◽

Smooth Muscle Actin ◽

Granulosa Cell Tumor ◽

Cell Tumor ◽

Placental Alkaline Phosphatase ◽

Alpha Smooth Muscle Actin ◽

Adult Type ◽

Left Testis ◽

Juvenile Type ◽

Potentially Malignant

Granulosa cell tumor (GST) is a sex-cord/stromal neoplasm of the gonads, more commonly arising in the ovaries, while approximately 80 cases have been reported in the testes. Out of these, 30 cases were of the adult type, while the remainder 50 cases were of the juvenile type. The latter mostly concerned infants and followed a benign course. However, the adult type testicular GCTs may be potentially malignant as it also happens in female patients with such neoplasms. We present a case of an adult type GCT located at the left testis. The patient was subjected to total orchiectomy and received no further treatment. Histology showed typical GCT histomorphology with Call-Exner bodies in some places. The immunoprofile of the tumor was CD99 (+), calretinin (+), inhibin (+), alpha smooth muscle actin (+), vimentin (+), ER (−), PR (−), keratin AE1/AE3 (−), alpha fetoprotein (−), CD117 (−), and placental alkaline phosphatase (−). Two years after surgery, the patient is alive and well with no signs of recurrence.

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Juvenile Type Ovarian Granulosa Cell Tumor

10.32388/nnr5j7 ◽

2020 ◽

Author(s):

Keyword(s):

Granulosa Cell ◽

Granulosa Cell Tumor ◽

Cell Tumor ◽

Ovarian Granulosa Cell ◽

Juvenile Type ◽

Ovarian Granulosa Cell Tumor

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Tumor de células de la granulosa juvenil de ovario. Presentación inusual. Reporte de un caso

Revista de Obstetricia y Ginecología de Venezuela ◽

10.51288/00810113 ◽

2021 ◽

Vol 81 (01) ◽

pp. 92-97

Author(s):

Ernesto Lara ◽

◽

Franco Calderaro ◽

Carmen Silva ◽

Johatson Freytez

Keyword(s):

Granulosa Cell ◽

Granulosa Cell Tumor ◽

Cell Tumor ◽

Adult Type ◽

Palpable Mass ◽

Juvenile Granulosa Cell Tumor ◽

Juvenile Type ◽

Precocious Pseudopuberty ◽

Ovary Tumor ◽

Immunohistochemical Studies

Granulose cell tumors represent 2% of ovarian tumors. They are classified as adult type and juvenile type. The juvenile type is associated with precocious pseudopuberty, irregular menstruation or nonspecific symptoms such as abdominal pain and palpable mass. More than 95% are confined to the ovary. A case of a 31-year-old patient is described. The patient consulted for 6-month evolution of increased abdominal volume and weight loss. Right ovary tumor was diagnosed. Tumor excision by gynecological laparotomy with positive frozen cut biopsy and surgical staging were performed. Pathological anatomy reported stromal tumor, and sexual cords suggestive of malignant juvenile granulose cell tumor. Immunohistochemistry reported positive inhibin B. It was concluded as stage IIIA2. This is a rare neoplasm with variable behavior. Accurate diagnosis is based on histological and immunohistochemical studies. Key words: Granulosa, Cell tumor, Juvenile granulosa cell tumor, Ascites, Diagnosis.

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