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Pelvic mass in Prepubertal Girls. Dr. Zohreh Yousefi Professor OF Mashhad University of Medical Sciences Gynecologist Oncologist. Origin of Pelvic mass gynecologic non gynecologic
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Pelvic mass in Prepubertal Girls Dr. Zohreh Yousefi Professor OF Mashhad University of Medical Sciences Gynecologist Oncologist
Origin of Pelvic mass gynecologic non gynecologic non gynecologic urinary tract Gasterointestinal Otheres
Wilms' tumor or nephroblastoma cancer of the kidneys that typically occurs in children Most nephroblastomas are unilateral Typical symptoms are: -large abdomen -abdominal pain -Fever -nausea and vomiting -blood in the urine (20% high blood pressure in some cases)
rupture of Wilms' tumor and hemorrhage risk of peritoneal dissemination of the tumor metastasis it is usually to the lung It is highly responsive to treatment 90% of patients surviving at least five years
Neuroblastoma the second most common solid tumour in childhood 8% of the total number of children's cancers Neuroblastoma is a cancer of specialised nerve cells called neural crest cells In some children, the neuroblastoma can occur in nerve tissue along side the spinal cord in the neck , chest, abdomen or pelvis
Signs and symptoms If the tumor is in the abdomen, may be swollen and they may complain of constipation or have difficulty passing urine blood pressure may also be high diagnose neuroblastoma blood, urine, or bone marrow tests x-rays; CT or MRI scans; and MIBG
The treatment of neuroblastoma depends on the age of the child the size position of the tumour the tumour biology (including the MYCN status) and whether the neuroblastoma has spread Treatment Surgery Chemotherapy
Appendicitis is most common in teens and young adults in their early 20s children younger than 4 years are at the highest risk for a rupture. Up to 80 percent of appendicitis cases in this age group occurred with rupture young children have fewer of the classic symptoms of nausea, vomiting and pain localized in the lower right portion of the abdomen than do teenagers and young adults making the diagnosis easy to miss or delay
ultrasound and CT scan images can be helpful, but are not always conclusive, even if they are available on an emergency basis CT scans in particular expose young children to radiation which should be avoided if possible The only absolute way to diagnose the condition is surgery
Gynecologic causes of pelvic mass Ovary Uterian Cervicovaginal
Müllerian duct abnormality congenital entities that result from nondevelopment, defective vertical or lateral fusion, or resorption failure of the müllerian ducts the majority are asymptomatic when a müllerian duct becomes obstructed may present with an abdominal mass and dysmenorrhea If the patient is not treated in a timely fashion the consequences can be severe, extending even to infertility
ultrasonography initially to delineate any abnormalities in the genital tract US cannot help identify the type of MDA In contrast, MRI is a valuable technique for noninvasive evaluation of the female pelvic anatomy and accurate MDA classification If obstruction is present surgical correction of the MDA may be required
Neonatal hematometrocolpos. (a) Transverse US scan shows a huge cystic mass (C) with a fluid-debris level (arrow)
Duplex uterus with an obstructed hemivagina in a 12-year-old girl Transverse US scan shows a normal left uterus (arrow) and a dilated right uterus (U).
Neonatal uterus Longitudinal US scan shows a prominent cervix (arrows) and a visible endometrium (arrowheads). Some fluid (F) is seen within the vagina
Wolffian duct Remnant • Mullerian Dact Remnant • Wolffian duct Remnant • They are mimic tumor of ovary • They are small but may enlarge and infarct • These are incidental finding at laparotomy and • cause no difficult or symtom
The gynecologic causes of a pelvic mass Neoplastic mass In younger girls Cervico-vaginal rare
The gynecologic causes of a pelvic mass Neoplastic mass In girls younger than 9 years of age, approximately 80% ovarian tumors were found to be malignant Fewer than 2% of ovarian malignancies occur in children and adolescents Non-epithelial tumors predominate
Germ cell tumors ½ -2/3 of ovarian neoplasmsin younger than 20 years of age Develop from primordial germ cells Termed as malignant, though do not have high malignant potential
Germ cell tumors Germinoma Teratoma
Typically grow rapidly- • 60% seen in first 2 decades of life • producing symptoms of distention and abdominal fullness • Torsion may occur, producing an acute abdomen • obvious malignancy with involvement of opposite ovary • ( Dysgerminoma) • all have a tendency to spread to the paraaortic lymph node • isosexual precocity reported
ultrasonographic appearance is very different with heterogeneous and solid components Karyotype Unilateral oophorectomy and lymphadenectomy followed by adjuvant chemotherapy Follow up necessary
Juvenile Granulosa Cell Tumors derive from granulosa cells tend to be of low malignity most of them have mixed components both solid and liquid Present as pelvic mass
Secrete estrogen and sometimes prolactin precocious pseudopuberty , galactorrhea measurement of anti-Müllerian hormone (AMH) and inhibin and carletenin
Treatment -unilateral oophorectomy -cystectomy and surgical staging careful examination of the contralateral ovary Postoperative follow-up consists of ultrasonography and tumor marker for several years -Good prognosis
NON NEOPLASTIC MASS Ovarian Cysts more common in the neonatal and adolescent periods ( 3 and 8 years ) decreases of frequency functional cysts in early childhood then increases as puberty
The Various Etiologies of OvarianCysts in Prepubertal Girls • Derived degenerated follicular cysts • ovarian gonadotropin stimulation • failure of follicular apoptosis • interaction with other hormonal secretion
Small cysts are more frequent than large cysts Small cysts asymptomatic discovered incidentally on ultrasonography elongated ovarian ligament of the abdominal location of tumor a predisposition to torsion
symptomatic cases: ( Abdomino -Pelvic pain) acute or sub acute non-specific signs (nausea, vomiting, urinary disorders) Precocious development may be transient onset breast development increasing during ovarian cyst formation
Benign Teratoma Dermoid cysts most frequent neoplasms in childhood mean age of diagnosis being 10 years heterogeneous appearance in ultrasonography a solid cystic component containing ectodermal tissue (skin, hair, dentin) calcifications are also clearly visible on plain radiographs
Treatment Preferable method in dermoid cyst in a young woman shell it out from the ovarian stroma and preserving functioning tissue
Autonomous Cyst McCune-Albright Syndrome is a sporadic disorder in small girls between 2 and 5 years ( early childhood) recurrent ovarian cysts diffuse anomalies
skin pigmentation skin spots café-au-lait polyostotic fibrous dysplasia characterizes the McCune-Albright syndrome symptoms bone and cutaneous signs detected several yearslater confirm the diagnosis by molecular studies ( mutations of Gs proteins )
The best known type of precocious pseudopuberty metrorrhagia and rapid breast development premature thelarche Central precocious puberty (elevated estradiol) Very low LH and FSH levels
Treatment Unilocular cysts <50mm may be followed conservatively This is a gonado-independent form of puberty usual puberty inhibiting treatments are ineffective Only aromatase inhibitors seem to have a certain efficacy
Management of ovarian cysts with endocrine syndrome hormonal investigations are necessary ultrasound-guided percutaneous aspiration Recurrence or surgically by laparaoscopy in the individual case.
Diagnostic Arguments of Ovarian Cysts in Prepubertal Girls • Limitation of pelvic capacity in prepubertal child • pelvic mass very quickly becomes abdominal location • Examination abdominal palpation • bimanual rectoabdominal • investigate the condition of the contralateral ovary
Transrectal ultrasonography For girl who had not intercourse No alternative imaging modality has demonstrated sufficient superiority to USG to justify its routine use
Ultrasonographic signs • of malignancy • Adnexal pelvic mass with • area of complexity • -Irregular border • -solid patterns within • the mass • -Dense multiple septae • color Doppler • hypervascularized tumor
Transvaginal Ultrasonography • Ultrasonographic signs of malignancy • Adnexal pelvic mass with area of complexity • Irregular border • solid patterns within the mass • Dense multiple septae
Tumor Markers a useful diagnostic aid in difficult to analyze by ultrasonography and in surveillance after tumor removal αFP in endodermal sinus tumor and embryonic carcinomas and immature teratomas. (β-HCG) in choriocarcinomas and dysgerminoma CA-125 levels either in peripheral blood or in the cyst fluid after aspiration LDH in dysgerminomas
Management • clinical signs • sonographic appearance • volume of the mass • finally its persistence • Unilocular cysts are virtually always benign • Will regress in 3 to 6 months • Close observation is recommended • surgical therapy for a functional ovarian mass • can result adhesions and adversely affect future fertility
surgical treatment is required • complicated cyst • hemorrhage • ovarian torsion • Solid masses • larger than approximately 8 cm