1.Phenotypic variation of 46,XX Late Identified Congenital Adrenal Hyperplasia among Indonesians
Achmad Zulfa Juniarto ; Maria Ulfah ; Mahayu Dewi Ariani ; Agustini Utari ; Sultana MH Faradz
Journal of the ASEAN Federation of Endocrine Societies 2018;33(1):6-11
Objectives:
To describe the phenotype variation in Indonesian 46,XX late-identified congenital adrenal hyperplasia(CAH) and the correlation between 17-hydroxyprogesterone (17-OHP) and genital virilization.
Methodology:
Retrospective study of 39 cases with five salt-wasting (SW) and 34 simple virilizing (SV) types.
Results:
The median age of the patients was 9.83 years (range, 0.58 to 44 years) with Prader score 2 to 5. Clitoromegaly (100%) and skin hyperpigmentation (87%) were the most common features. Lack of breast development(Tanner 1 to 2) and menstrual disorders occurred in 9 patients (teenagers and adults). Short stature (6), low voice (14),prominentAdam’s apple (9) and hirsutism (4) were found only in SV types Rapid growth (7) and precocious puberty (8)were identified in children. Male gender on admission was found in 13 patients. The mean of 17-OHP level was 304.23nmol/L [standard deviation (SD) 125.03 nmol/L]. There was no correlation between 17-OHP levels and virilization(r=0.19, p>0.05).
Conclusion
Late-identified CAH showed severe virilization and irreversible sequelae, with clitoromegaly and skinhyperpigmentation as the most commonly seen features. Masculinization of CAH females created uncertainty withregard to sex assignment at birth, resulting in female, male and undecided genders. There is no significant correlationbetween 17-OHP levels with the degree of virilization in CAH females
Phenotype
;
Virilism
3.A Case of Ovarian Steroid Cell Tumor with Obesity.
Seong Seog SEO ; Jung Pil LEE ; Hee Jae JOO ; Eun Ju LEE ; Ho Bin KIM ; Ki Hong CHANG ; Hee Sug RYU
Korean Journal of Obstetrics and Gynecology 2004;47(5):1011-1016
Ovarian steroid cell tumors are composed exclusively of cells that have the histologic features of steroid hormone secreting cells. And these are rare lesions and have been divided into four subtyes according to their size, location in the ovary, and presence or absence of crystals of Reinke in the cytoplasm as follows: stromal luteomas, hilus cell tumors, Leydig cell tumors (non-hilar type), and steroid cell tumors not otherwise specified. Steroid cell tumors often secret androgens, and manifest themselves with symptoms of virilization. Other presenting manifestations include hirsutism, amenorrhea, obesity, hypertension and alopecia. We experienced a case of ovarian steroid cell tumor, manifested by obesity and amenorrhea and present with a brief review of the literatures.
Alopecia
;
Amenorrhea
;
Androgens
;
Cytoplasm
;
Female
;
Hirsutism
;
Hypertension
;
Leydig Cell Tumor
;
Luteoma
;
Obesity*
;
Ovary
;
Virilism
4.A rare case of virilizing ovarian steroid cell tumor in a 46 year-old woman: A case report and review of literature.
Andres Audrey Angeli O. ; Irabon Ina S. ; Manabat Manuel S.
Philippine Journal of Obstetrics and Gynecology 2014;38(4):44-49
Virilization is the masculinization and enhancement of male secondary sexual characteristics in females. The etiology may be of adrenal or ovarian in origin. This case report shows a 46 year old woman who presented with defeminizing and virilizing symptoms. Further laboratory investigations revealed increased serum androgen levels and normal CT scan of the adrenals and kidneys. An ovarian mass was confirmed by transrectal ultrasonography. Following a total abdominal hysterectomy and bilateral salpingooophorectomy, histopathological and immunohistochemistry studies on the left ovarian mass confirmed an androgen-secreting, steroid-cell tumor, not otherwise specified (NOS). Serum testosterone values abruptly declined to normal levels within 1 month post-surgery. This paper likewise discusses an extensive review of literature regarding this rare ovarian tumor.
Human ; Female ; Middle Aged ; Virilism
5.Functioning Adrenocortical Carcinoma in a Child.
Myeong Heon JIN ; Duck Ki YOON ; Young Su KO ; Jae Heung CHO ; Dong Sun KIM
Korean Journal of Urology 2002;43(7):638-640
Adrenocortical carcinoma is a rare tumor in children. This tumor is more likely to be hormonally active in children than in adults and tends to cause a variety of symptoms. These tumors are usually diagnosed at the advanced stages and have a dismal prognosis. Here we report a case of a functioning adrenocortical carcinoma in a child with a review of the relevant literature.
Adrenocortical Carcinoma*
;
Adult
;
Child*
;
Humans
;
Prognosis
;
Virilism
6.Diagnosis of an indistinct Leydig cell tumor by positron emission tomography-computed tomography
Jinkyoung KONG ; Yoo Mee PARK ; Young Sik CHOI ; SiHyun CHO ; Byung Seok LEE ; Joo Hyun PARK
Obstetrics & Gynecology Science 2019;62(3):194-198
A 51-year-old perimenopausal female patient presented with hirsutism and voice thickening which was started approximately one and a half years ago. Her initial hormone assay revealed elevated plasma testosterone, 5a-dihydrotestosterone, and dehydroepiandrosterone (DHEA) levels and therefore androgen-secreting tumor was first suspected. However, the lesion was inconspicuous on transvaginal sonography, abdominal-pelvic computed tomography (CT) scan, and pelvic magnetic resonance (MRI) imaging. Consequently, 18F-fluorodeoxyglucose (FDG) positron emission tomography-CT was performed, which localized the lesion as a focal FDG uptake within the right adnexa. Total laparoscopic hysterectomy with bilateral salpingo-oophorectomy was performed, and although visible gross mass lesions were not observed intraoperatively, pure Leydig cell tumor was pathologically confirmed within the right ovary. Plasma testosterone, 5a-dihydrotestosterone, and DHEA levels were normalized postoperatively. Clinical signs of virilization were also significantly resolved after 3-months of follow-up.
Dehydroepiandrosterone
;
Diagnosis
;
Electrons
;
Female
;
Follow-Up Studies
;
Hirsutism
;
Humans
;
Hysterectomy
;
Leydig Cell Tumor
;
Middle Aged
;
Ovary
;
Plasma
;
Sertoli-Leydig Cell Tumor
;
Testosterone
;
Virilism
;
Voice
7.Two Cases of Adrenogenital Syndromes Developed in Sisters.
Bong Joo KIM ; Yang Il PARK ; Byung Kap MIN
Korean Journal of Urology 1988;29(4):651-655
Virilization in infants and children is most commonly associated with congenitalbilateral cortical hyperplasia in the adrenogenital syndrome. Two cases of adrenogenital syndromes developed in sisters of a 15 and a 13 year-old girlsare presented with brief review of literatures.
Adolescent
;
Adrenogenital Syndrome*
;
Child
;
Humans
;
Hyperplasia
;
Infant
;
Siblings*
;
Virilism
8.A case of turner mosaicism with virilization.
Eun Seon IM ; Chang Woo CHOO ; Sang Wook KIM ; Jung Yeob SUNG ; Jeong Woo PARK ; Hae Ryoung KIM ; Byung Chul JEE
Korean Journal of Obstetrics and Gynecology 2009;52(6):671-675
A 17-year-old girl presented with primary amenorrhea, short stature, and clitomegaly. Her karyotype showed Turner mosaicism of 45,X/46,XY,idic(Y)(q11.23)del(Y)(q11.23). Laparoscopic bilateral gonadectomy was performed and there was testicular tissue in left ovary.
Adolescent
;
Amenorrhea
;
Female
;
Humans
;
Karyotype
;
Mosaicism
;
Ovary
;
Virilism
9.A case of hyperinsulinemic obese female adolescent with virilization.
In Mee BAEK ; Ji Yeon LIM ; Hey Soon PARK
Journal of the Korean Academy of Family Medicine 1998;19(12):1419-1427
BACKGROUND: Being obese during adolescence leads to undue physical or psychological problems and may increase the incidence of cardiovascular disease or endocrinological disorders. Recently authors have experienced a case of hyperinsulinemic obese girl with virilization. We report it with a review of the literature. CASE: A 17-year old female came into 'obesity clinic' of Asan Medical Center due to weight gain. She had virilizing feature, hirsutism, underdeveloped female sexual characteristics, and acanthosis nigricans. Work-up by laboratory tests and imaging studies showed very severe obesity with metabolic disturbances, and hyperandrogenism with hyperinsulinemia. Treatment for obesity was multidisciplinary method including behavior modification, calorie restriction, exercise, and medication with fluoxetine 40mg po qd, and for hyperandrogenism, provera 10mg po qd was described. CONCLUSIONS: Severe hyperinsulinemia in obese female leads to male-type hirsutism, disturbance of menstrual cycle, abdominal obesity, and cardiovascular disorders. One of the physical findings of hyperinsulinemia or insulin resistance is acanthosis nigricans. So, if an female obese patient have acanthosis nigricans with hyperinsulinemia, should be assessed and treated for risk factors of cardiovascular disorders and hormonal disturbances.
Acanthosis Nigricans
;
Adolescent*
;
Behavior Therapy
;
Cardiovascular Diseases
;
Chungcheongnam-do
;
Female*
;
Fluoxetine
;
Hirsutism
;
Humans
;
Hyperandrogenism
;
Hyperinsulinism
;
Incidence
;
Insulin Resistance
;
Medroxyprogesterone Acetate
;
Menstrual Cycle
;
Obesity
;
Obesity, Abdominal
;
Obesity, Morbid
;
Risk Factors
;
Virilism*
;
Weight Gain
10.MR Imaging of Pregnancy Luteoma: a Case Report and Correlation with the Clinical Features.
Hung Wen KAO ; Ching Jiunn WU ; Kuo Teng CHUNG ; Sheng Ru WANG ; Cheng Yu CHEN
Korean Journal of Radiology 2005;6(1):44-46
We report here on a 26-year-old pregnant female who developed hirsutism and virilization during her third trimester along with a significantly elevated serum testosterone level. Abdominal US and MR imaging studies were performed, and they showed unique imaging features that may suggest the diagnosis of pregnancy luteoma in the clinical context. After the delivery, the serum testosterone level continued to decrease, and it returned to normal three weeks postpartum. The follow-up imaging findings were closely correlated with the clinical presentation.
Adult
;
Contrast Media
;
Diagnosis, Differential
;
Female
;
Gadolinium DTPA/diagnostic use
;
Hirsutism/etiology
;
Humans
;
Luteoma/complications/*diagnosis
;
Magnetic Resonance Imaging
;
Ovarian Neoplasms/complications/*diagnosis
;
Pregnancy
;
Pregnancy Complications, Neoplastic/*diagnosis
;
Pregnancy Outcome
;
Ultrasonography, Prenatal
;
Virilism/etiology