1.A bearded indian female: A rare presentation of Cushing's Syndrome
Rajesh Jain ; SV Madhu ; Saket Kant ; Ved Prakash ; Vinod Kumar
Journal of the ASEAN Federation of Endocrine Societies 2013;28(1):91-92
A 16-year-old Indian girl presented with increased facial hair growth, weight gain, amenorrhea and generalized weakness for the last 3 months. On examination she was found to have severe hirsutism, her modified Ferriman-Gallwey score was 24/36, she had broad purple striae on abdomen, hypertension and proximal myopathy. On investigations, the patient was found to have ACTH dependent Cushing's syndrome
Cushing Syndrome
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Hirsutism
3.Virilizing tumor in pregnancy: a case report
Santoyo-Dancel Mary Ann ; Dee Marlyn T.
Philippine Journal of Reproductive Endocrinology and Infertility 2008;5(1):51-54
Virilizing tumors during pregnancy are extremely rare. This case of a 33 year old, gravid 3 para 2, presented with hirsutism and clitoromegaly at 5 months age of gestation. Her past medical and menstrual histories were non-contributory. Ultrasound done during her prenatal check-up at 34 weeks age of gestation revealed an ovarian new growth on the left ovary features suggestive of a benign nature. On her 38th week of pregnancy, LTCS III with right tubal ligation and left salpingooophorectomy were performed and a baby boy weighing 3000 grams without any gross abnormalities was delivered. Histopathologically, the tumor proved to be a benign mucinous cystadenoma. This paper presented an ovarian mucinous cystadenoma with virilizing features that are transient and reversible. Therefore, an ovarian neoplasm should always be considered as a differential diagnosis for causes of virilization during pregnancy.
Human
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Female
;
Adult
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HIRSUTISM
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PREGNANCY
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CYSTADENOMA, MUCINOUS
4.Correlation of visual (modified Ferriman–Gallwey scoring) and biochemical evaluation of hirsutism in polycystic ovary syndrome patients in a tertiary hospital: A cross-sectional study.
Marth Louie Zorilla TARROZA ; Debby F. PACQUING-SONGCO ; Brenda Bernadette B. ZAMORA
Philippine Journal of Obstetrics and Gynecology 2025;49(1):3-9
BACKGROUND
Polycystic ovarian syndrome (PCOS) is a common gynecologic endocrine disorder affecting between 2.2% and 26% of the population. It is typically characterized by hirsutism and signs of ovulatory dysfunction. Hirsutism is defined as the presence of excess body or facial terminal hair growth in females, following a male-like pattern. It is diagnosed using visual assessment methods, such as the modified Ferriman–Gallwey (mFG) scoring system, and biochemical tests, including measurements of total testosterone (tT) and the free androgen index (FAI).
OBJECTIVESThe general objective of the study is to identify the correlation of visual scoring with the biochemical evaluation of hirsutism. Specific objectives include (1) to describe the visual and biochemical scores of hirsutism in PCOS patients and (2) to determine a cutoff score for the visual scoring of hirsutism among Filipinos.
METHODOLOGYThis is a cross-sectional study done in a tertiary hospital. Ethical approval was obtained for this study. Patients who satisfied the inclusion criteria were included in the study. Age, height, weight, body mass index (BMI), and OB score were noted. Visual scoring for hirsutism using the mFG scoring system was performed. Blood extraction was done for testosterone and sex hormone-binding globulin tests. FAI was then computed and correlated with the mFG scores.
RESULTSA total of 52 patients were identified. A positive correlation is noted between the mFG with testosterone and FAI. A positive correlation was also noted between the BMI with testosterone and FAI. An mFG value of >4 is an acceptable cutoff for Filipinos.
CONCLUSIONThe study showed as the mFG score increases, FAI and tT levels also increase. It was also noted that as BMI increases, the FAI and tT levels are also expected to increase. It can also be concluded that a lower mFG cutoff value, >4, is applicable for Filipinos.
Human ; Female ; Hirsutism ; Hyperandrogenism ; Polycystic Ovary Syndrome
5.A Case of Partial Lipodystrophy.
Hae Soo MOK ; Kyung Sool KWON ; Tae Ahn CHUNG
Korean Journal of Dermatology 1985;23(6):817-821
Partial lipodystrophy is an uncommon disorder primarily affecting women, with onset usually in childhood, characterized by slowly progressive, symrnetrical loss of aubcutaneous fat from the upper half of the body. We present a case of partial lipodystrophy in a 43-year-old woman with multiple depressed lesion on the face and reticulated atrophic lesions on the upper trunk and u]pper extremities. Typically, her face was the first part of the body so affected, giving it a characteristic cadeverous appearance, and gradu ally spreaded to the upper half of t2e body. Sirnultaneously, there was an accumulation of fat over the lower part of the body. She was generally otherwise well, although there had been an association with hyperpigmentation, hirsutism, arthralgia, thyroid disoraer, and low serum CR(45mg/dl), Riopsy specimens of iace and back showed lack of subcutaneous fat, but in the other section of the face showed hydropic degeneration of basal cells and inflammatory infiltrate in the dermis.
Adult
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Arthralgia
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Dermis
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Extremities
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Female
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Hirsutism
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Humans
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Hyperpigmentation
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Lipodystrophy*
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Subcutaneous Fat
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Thyroid Gland
6.Three cases of Cornelia de Lange syndrome.
Sang Min SEONG ; Jun Sung LEE ; Dong Bock LEE ; Kyung Tai WHANG
Journal of the Korean Pediatric Society 1978;21(3):232-238
We have experienced 3 cases of Cornelia de Lange syndrome in Korean female infants. They showed typical clinical features of a microbrachycephaly, hirsutism and characteristic face with low forehead bushy eye brows, antimongolian slant, large and depressed briedge of nose, thin protruding lips with down turning of the corners and micrognathia. They also had skeletal abnormalities and chromosomal abnormalities. The diagnosis was established by clinical, laboratory and X-ray findings. The brief review of literature was made.
Chromosome Aberrations
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De Lange Syndrome*
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Diagnosis
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Female
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Forehead
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Hirsutism
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Humans
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Infant
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Lip
;
Nose
7.CYP11alpha (tttta)n Microsatellite Polymorphism in Korean Patients with Polycystic Ovary Syndrome.
Jin Ju KIM ; Young Min CHOI ; Sang Ho YOON ; Seon Ha CHOUNG ; Doo Seok CHOI ; Seung Yup KU ; Byung Chul JEE ; Chang Suk SUH ; Seok Hyun KIM ; Jung Gu KIM ; Shin Yong MOON
Korean Journal of Fertility and Sterility 2004;31(4):245-252
OBJECTIVES: To investigate the distribution and functional significance of CYP11alpha (tttta)n microsatellite polymorphism in Korean patients with polycystic ovary syndrome MATERIALS AND METHODS: Analysis of CYP11alpha(tttta)n microsatellite polymorphism was carried out on DNA samples from 97 patients with polycystic ovary syndrome and 70 normal controls. Comparison were done between PCOS patients and controls concerning CYP11alpha (tttta)n microsatellite polymorphism genotype or allele frequencies. RESULTS: The most frequent allele observed in the controls was an allele with six repeats (60.7%). Significant difference in the frequency of genotype (4R (-) genotype) having no copy of four-repeat-allele were observed between PCOS patients and controls (66.0% vs 34.0%, p=0.038, OR=1.939). But no significant difference was observed in the serum levels of total testosterone or free testosterone between 4R (+) genotype and 4R (-) genotype among PCOS patients. However, hyperandrogenic PCOS patients with 4R (+) genotype showed a higher serum testosterone levels compared to controls (mean+/-S.D: 0.49+/-0.21 ng/ml vs 0.37+/-0.18 ng/ml, p=0.037). CONCLUSION: The alleleic distribution of CYP11alpha (tttta)n microsatellite polymorphism in Korean subjects were different from those reported in Caucasians. CYP11alpha (tttta)n microsatellite polymorphism was associated with polycystic ovary syndrome in the Korean population, and may play a role in the synthesis of androgens in patients with polycystic ovary syndrome.
Alleles
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Androgens
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DNA
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Gene Frequency
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Genotype
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Hirsutism
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Humans
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Hyperandrogenism
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Microsatellite Repeats*
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Polycystic Ovary Syndrome*
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Testosterone
8.Cornelia de Lange Syndrome.
Hwa Jung YOON ; Ai Lan KIM ; Whan Kok YONG ; Sung Il AHN
Journal of the Korean Pediatric Society 1980;23(6):479-485
The Cornelia de Lange syndrome is characterized by severe growth and mental retardations and a cluster of minor malformations, the facial appearance being most characteristic. In the present paper, we shall report I case of this syndrome in Korean male infant and the variability of de Lange syndrome is discussed. The bady showed hirsutism, low forehead coved with lanugo-like hair, bushy eyebrows that meet in the midline, long curely eyelashes as well as low pitched, growling cry and skeletal abnormalities of hand bones. There is no positive family history and the karyotype was normal. Although the de Lange syndrome has received more interest there is no agreement as to the possible cause.
De Lange Syndrome*
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Eyebrows
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Eyelashes
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Forehead
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Hair
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Hand Bones
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Hirsutism
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Humans
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Infant
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Karyotype
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Male
9.Two Cases of Acquired Localized Hypertrichosis Associated with Cellulitis and Contusion.
Sang Ho OH ; Sung Bin CHO ; Kee Yang CHUNG
Korean Journal of Dermatology 2002;40(10):1279-1281
Hypertrichosis refers to the increase of hair density or length beyond the accepted limits of normal for a particular age, race, or sex. It is an overgrowth of hair in androgen-independent areas and it differs from hirsutism, which refers to hair growth in women in areas of the body where hair growth is under androgen control. It may be classified into congenital and acquired types according to age of development, and localized or generalized types according to the range of involvement. Acquired localized hypertrichosis may occur secondary to infective or inflammatory diseases, traumas, drugs, fracture and cast, lymphedema, sympathetic dystrophy, topical steroid application, denervation, or congenital AV fistula. Any situation that results in persistent and repetitious inflammation in the dermis or individual susceptibility may cause hypertrichosis. We report two cases of acquired localized hypertrichosis associated with cellulitis and contusion.
Cellulitis*
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Continental Population Groups
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Contusions*
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Denervation
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Dermis
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Female
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Fistula
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Hair
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Hirsutism
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Humans
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Hypertrichosis*
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Inflammation
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Lymphedema
10.Hyperandrogenism in Women: Polycystic Ovary Syndrome.
Hanyang Medical Reviews 2012;32(4):197-202
Hyperandrogenism refers to classical androgen-dependent signs such as hirsutism, acne and androgenetic alopecia. Disorders that result in androgen excess include specific identifiable disorders (i.e. disorders of inclusion), but the great majority of women presenting with hirsutism and other symptoms or signs of hyperandrogenism suffer from polycystic ovary syndrome (PCOS). Hirsutism is the main hyperandrogenic symptom, defined as an excess of body hair in androgen-sensitive regions of skin in women. In this review, I attempt to focus on the pathogenesis of hirsutism, as well as clinical and biochemical features that are important in choosing therapeutic options. PCOS is the most common disorder of premenopausal women, affecting 4 to 8% of this population, and therefore, diagnostic issues of PCOS in Korean women will be addressed, specifically the reproductive and metabolic derangements and criteria for hyperandrogenism based on hirsutism and serum androgen concentrations.
Acne Vulgaris
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Alopecia
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Female
;
Hair
;
Hirsutism
;
Humans
;
Hyperandrogenism
;
Polycystic Ovary Syndrome
;
Skin