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خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده : 3 مورد
نسخه الکترونیک
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Comparison of findings in SCSTs[1-3]

Comparison of findings in SCSTs[1-3]
Tumor Age at presentation Characteristic features of the ovarian mass Hormonal effects* Other potential tumor markers Behavior
Fibroma
  • Usually postmenopausal women (average age 48)
  • Gross: Firm white tumor.
  • U/S: Usually unilateral hyper- or hypoechoic mass, which may be calcified and/or exhibit cystic degeneration. Ascites is present in 10 to 15% of cases and hydrothorax in 1%, especially with larger lesions.
  • None
  • CA 125
  • Benign
Thecoma
  • Postmenopausal women 
  • Gross: Yellow, can be very large (40 cm).
  • U/S: Unilateral and solid. Ascites is rare.
  • Signs/symptoms of excess estrogen. Endometrial hyperplasia and carcinoma are present in approximately 15 and 20 to 25% of cases, respectively.
  • N/A
  • Benign
Fibrosarcoma
  • Postmenopausal women
  • Gross: Lobulated.
  • U/S: Unilateral, solid but may have areas of hemorrhage and necrosis.
  • None
  • N/A
  • Malignant
Luteinized thecoma associated with sclerosing peritonitis
  • Broad age range
  • Gross: Surface may be smooth, polypoid, lobulated, or cerebriform.
  • U/S: Bilateral and solid. Massive ascites is common.
  • Hormonal manifestations are usually absent. Rare cases associated with estrogen or androgen production.
  • N/A
  • Benign. However, it can be associated with significant morbidity and occasional death due to severe adhesive disease and bowel obstruction.
Granulosa cell tumor
  • Adult subtype occurs most commonly in middle-aged and older women (median age 50 to 54 years) and comprises 95% of these neoplasms
  • Juvenile subtype typically develops before puberty, and comprises 5% of all granulosa cell tumors
  • Gross: Appearance is variable; usually large (mean diameter 12 cm but may be as large as 30 cm), tan or yellow, and either soft or firm.
  • U/S: Usually unilateral, echogenic, septated cystic, or solid mass. May resemble a mucinous cystadenoma or be filled with serous fluid or clotted blood. Ascites may be present. Torsion, intraneoplasmal hemorrhage, or tumor rupture with hemoperitoneum may be seen.
  • Signs/symptoms of excess estrogen in over one-half of patients. Endometrial hyperplasia/intraepithelial neoplasia in 25 to 50% and endometrial carcinoma in 5 to 10%. The endometrial adenocarcinomas are usually early stage and well differentiated.
  • Virilization is possible, but rare.
  • Inhibin
  • AMHΔ
  • CA 125
  • Malignant
Sertoli-Leydig cell tumor
  • Usually in the second and third decades of life
  • Approximately 75% occur in women under age 40 years (mean age at diagnosis is 25), but they occur in all age groups
  • Gross: Yellow and lobulated, with a smooth external surface. Well-differentiated neoplasms with retiform components are often soft and spongy, while poorly differentiated subtypes may have areas of hemorrhage and necrosis.
  • U/S: Often large (average 16 cm in maximal diameter but may be >20 cm). Most are unilateral and solid but may contain areas of closely packed small cysts.
  • At least one-third of patients have virilization. Less than one-third of patients have signs/symptoms of excess estrogen.
  • AFP
  • Inhibin¶
  • CA 125 (rare)
  • Benign or malignant
Sex cord tumor with annular tubules (sporadic)
  • Average age 36
  • Gross: Often large.
  • U/S: Unilateral, uncalcified.
  • Almost all patients have signs/symptoms of excess estrogen.
  • N/A
  • Benign or malignant
Sex cord tumor with annular tubules (associated with Peutz-Jeghers syndrome)
  • Average age 27 (ie, younger than sporadic SCTAT)
  • Gross: Usually small (<3 cm).
  • U/S: Bilateral, multifocal, calcified.
  • Almost all patients have signs/symptoms of excess estrogen.
  • N/A
  • Usually benign
Sertoli cell tumor
  • Usually women of reproductive age, but may occur in children as young as age 2 and postmenopausal women
  • Gross: Yellow to brown.
  • U/S: Usually unilateral, solid, but may have several cystic areas.
  • Approximately one-half produce functional hormones. Most commonly signs/symptoms of excess estrogen, but virilization can occur. Rarely both estrogens and androgens are produced.
  • Renin (rare)
  • Benign or malignant
SCST: sex cord-stromal tumor; U/S: ultrasound; CA 125: cancer antigen 125; N/A: not applicable; AMH: anti-müllerian hormone; SCTAT: sex cord tumors with annular tubules; AFP: alpha-fetoprotein.
* Signs/symptoms of excess estrogen: abnormal uterine bleeding, menorrhagia, postmenopausal bleeding, breast tenderness, and precocious puberty in children. Signs/symptoms of excess androgen (virilization): oligomenorrhea, amenorrhea, breast atrophy, hirsutism, deepening voice, male pattern baldness, acne, and clitoral enlargement.
¶ Inhibin usually becomes undetectable after menopause, unless produced by certain ovarian tumors, mostly mucinous epithelial ovarian carcinomas and granulosa cell tumors. Inhibin exists as two different isoforms, inhibin A and inhibin B, consisting of alpha and beta subunits. The alpha subunit is the same for both isoforms, while the beta subunits differ. In general, both inhibin A and inhibin B should be ordered, if possible.  The free alpha subunit can also be measured.
Δ Anti-müllerian hormone (AMH, also known as müllerian inhibiting substance [MIS]) is produced by granulosa cells in the developing follicles. AMH is typically undetectable in postmenopausal women. An elevated AMH level appears to be highly specific for ovarian granulosa cell tumors.
AFP is often elevated (range from 4 to 14,000 ng/mL). However, it should be noted that the more common ovarian tumors that classically produce AFP are yolk sac tumors and embryonal carcinomas.
References:
  1. Al-Hussaini M, Al-Othman Y, Hijazi E, McCluggage WG. A Report of Ovarian Sertoli-Leydig Cell Tumors With Heterologous Intestinal-type Glands and Alpha Fetoprotein Elevation and Review of the Literature. Int J Gynecol Pathol 2018; 37:275.
  2. Lim D, Oliva E. Ovarian sex cord-stromal tumours: an update in recent molecular advances. Pathology 2018; 50:178.
  3. Young RH, Scully RE. Ovarian Sertoli-Leydig cell tumors. A clinicopathological analysis of 207 cases. Am J Surg Pathol 1985; 9:543.
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