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PEDIATRIC GYNECOLOGY. By DR. ARCHANAVIKRAM ASST. PROF DEPT OF OBG. INTRODUCTION. ▪ An awareness of the problems that are unique to pediatric and adolescent gynecology is invaluable for proper management of the young patient .
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PEDIATRIC GYNECOLOGY By DR. ARCHANAVIKRAM ASST. PROF DEPT OF OBG
INTRODUCTION ▪ An awareness of the problems that are unique to pediatric and adolescent gynecology is invaluable for proper management of the young patient . Particular care is essential in addressing gynecologic concerns in this age group because both physical and emotional trauma may be inadvertently inflicted .
Normal findings in a pediatric patient . A mucoid vaginal discharge . An introitus that is located more anteriorly than normal and a clitoris that is more prominent than normal ( 1 to 2 cm ) . A redundant hymen that may protrude on straining and that remains essentially the same size until 10 years of age . A vaginal epithelium that is uncornified and erythematous with an alkaline pH . A small uterus ( 2.5 to 3 cm ) in length . A cervical os that is covered with glandular epithelium and normally appears red ( ectropion )
Trauma Tears , abrasions , ecchymoses , and hematomas are common in preadolescent girls . The incidence is highest in children between 4 and 12 years of age . The most common causes of injury are sexual abuse, straddle injuries , accidental penetration , sudden abduction of the extremities , and pelvic fractures .
Management . Visualize vagina to locate sources of bleeding - Superficial abrasions and lacerations of the vulva , if not actively bleeding , can be cleaned and left alone . In sexual abuse , antibiotic therapy is advised as prophylaxis against sexually transmitted diseases .
Labial agglutination • Clinical picture Adhesion of the labia minora in the midline is the usual presentation. • The agglutination encourages retention of urine and vaginal secretions and can lead to vulvovaginitis or urinary tract infection. • Management • If asymptomatic, improved hygiene may be all that is necessary. • Lubrication of the labia with a bland ointment. • Topical estrogen. • Surgical separation is rarely necessary.
Clinical Picture • A mucoid discharge is common in infants for up 2 weeks after birth;it result from maternal estrogen. • It is also a common finding in prepubertal girls, who experience increased estrogen production by maturing ovaries. • Pathologic discharge may result from any of the following conditions: • Infections with organisms, such as E.coli, Proteus, Pseudomonas. • Hemolytic streptococcal vaginitis. • Monilialvaginitis. • A foreign body.
Managment • Conservative management is advisable, as follows: • Culture to identify causative organisms. • Urinanalysis to rule out cystitis. • proper hygiene. • Perianal examination with transparent tape to test for pinworms. • In cases of persistent discharge, examination under anesthesia is indicated to rule out foreign body.
Neoplasms A. Tumors of the vagina
Clinical Picture • It appears as an edematous, grape-like mass that bleeds readily on touch. It is usually multi-centric and extension is usually local, with rare instances of distant metastases. • Management A combination of surgery and chemotherapy is most commonly used.
B. Ovarian Tumors • Clinical Picture: • Non-germ cell origin • Lipoid cell tumors( estrogen producing) • Granules theca cell tumors(estrogen producing) • Germ cell origin • Benign cystic teratomas. • Benign cysts. • Arrhenoblastomas (androgen producing). • Dysgerminomas and gonadoblastomas ( tumors of dysgenetic gonads). • Endodermal carcinomas ( human chorionic gonadotropin [hcg]- secreting tumors). • Immature teratomas.
Managment • Treatment is surgical, alone or in combination with chemotherapy, depending on the tumor. Radiation is sometimes used to treat dysgerminomas.
A. Mullerian agenesis (Mayer-von Rokitansky- Kauster-Hauser [MRKH] syndrome) Amenorrhea Ovarian development is normal The uterus is usually absent Vaginal agenesis(normal 46xx karyotype) Management Surgical creation of neovagina
B-Ectopic ureter with vaginal terminus • Ectopic ureter,the most common cause of vaginal cysts in infants. • Irritation • Vaginitis may be presenting signs • Hydroureter • Hydronephrosis
Diagnosis • Intravenous pyelography, which allows visualization of the entire urinary tract . Management • Resect the lowest portion of the ureter and implant it into the bladder . • Remove the ureter and associated portion of the kidney
C-vaginal ectopic anus • Imperforate anus associated with rectovaginal communication Management • Surgical correction is indicated
V-Developmental defects of the External Genetalia (Ambiguous Genitalia) • hormones with androgenic activity are present during development of female fetus, or androgens or androgen activity are absent during development of male fetus.
Congenital adrenal hyperplasia (CAH) • Cortisol and aldosterone pathways are impaired . • The 21-hydroxylase defect is the most common cuse of distinct virilization of the female newborn. • The chromosomes,gonads,and internal genitalia are female,but the external genitalia are virilized to varying degrees. • Urogenital orifice closed . • Clitoral enlargement and accentuation of labial folds are characteristic .
Adrenal tumors • These tumors,which may cause virilization of the external genitalia after infancy, should be suspected in children with high levels of dehydroepiandrosterone sulfate (DHEAS). C-maternal ingestion of androgenic substances Causal agents identified include androgens,danazol,any synthetic progestins(in doses much higher than in oral contraceptive pills).
Clinical picture • The clitoris is enlarged and the labia may be fused, but the vagina, tubes, and uterus are normal . • Growth and development are normal, and progressive viritization does not occur. Diagnosis • The condition can be diagnosed based on positive history and on exclusion. Management • Clitoral reduction and surgical correction of the fused labia maybe necessary.
Androgen insensitivity syndrome • A 46xy genotype is present, but a female phenotype develops. • Androgens are produced by the testes (which develop in the presence of y chromosome) and by adrenal glands. • External genitalia are feminized • No uterine, cervical,upper vaginal, or fallopian tube development. • A short vagina . • Labia, may contain testes.
Diagnosis • Primary amenorrhea. • A blind or absent vagina. • Lack of pubic and axillary hair development. Breast development does occur because estrogen concentration is high due to conversion of testosterone produced after puberty. • A karyotype-This syndrome is distinguished from MRKH by absent axillary and pubic hair development and high testosterone level. • Management • The gonads should be removed because of an incresed risk of malignancy
True hermaphroditism Clinical picture • The genotype is 46xx • The external genitalia may appear male,female,or ambiguous. • Both male and female internal genitalia may be present. Management • The genitlia that are inconsistent with sex assignment should be surgically removed or modified.
G-maternal virilizing tumor during pregnancy(luteoma of pregnancy)
Abnormal pubertal development Delayed puberty: • Hypergonadotropic hypogonadism : It includes conditions in which the ovaries or gon ads are not functioning. • Hypogonadotropic hypogonadism : The ovary is normal ,however, there is a lack of production of hormonal stimulation from the hypothalamus, includes Kallmann syndrome (isolated GnRH deficiency ) Eugonadotropic: constitutional delay accounts for 10% to 20% of cases .
Managment • Treatment is based on the etiology of the delay . • In cases of gonadal dysgenesis when a Y chromosome or fragment of a Y chromosome is present , the gonads should be removed at diagnosis because of the risk of neoplastic degeneration . • Otherwise , hormone replacement with estrogen and subsequently both estrogen and progesterone , is required to promote sexual development and menarache.
Special problems of the adolescent A. Dysmenorrhea : • Primary dysmenorrhea accounts for most cases and is attributed to increased prostaglandin production with menses in the presence of normal anatomy . • Secondary dysmenorrhea results from conditions such as endometriosis and anomalies with obstruction in a portion of the outflow tract . Clinical picture • Sever , cyclic , cramp-like pain located in the lower abdomen and pelvis is associated with menses
Managment • First-line therapy is prostaglandin inhibitors (nonsteroidal anti-inflammatory drugs [NSAIDs] • If the symptoms are not reduce- start oral contraceptives or obtain a pelvic ultrasound to evaluate for abnormal anatomy depending on the loction, progression, and severity of the symptoms • Laparoscopy is recommended if medical treatment fails to control the symptoms .
Precocious Puberty Def – appearance of appropriate secondary sexual characters before age of 8 yrs & occcurence of menstruation before 10 yrs of chronological age. Causes • Constitutional • Hypothalamic neoplasm- hamartoma • Pituitary tumors • Ovarian feminizing tumor • Adrenal tumors • Infections – meningitis, encephalitis • Mc Cune Albright syndrome • Iatrogenic
Dysfunctional uterine bleeding • DUB is defined as excessive , prolonged , or irregular bleeding not associated with an anatomic lesion. • Most adolescent girls have anovulatory menstrual periods for the first 2 to 3 years following menarche . • The cause of DUB in 75% of cases is an immature hypothalamic –pitutary axis resulting in anovulation • Other cases include psychogenic factors ,juvenile hypothyrodism and coagulation disorders (von willebrand disease )
Clinical picture • Menometrorrhagia ( irregular , heavy bleeding) is the most characteristic symptom . • Bleeding can be prolonged and heavy in some cases leadng to sever anemia . • The condition is usually self – limited Management Cyclic hormonal manipulation with progestins or comined oral contrceptive pills .