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1.
Tunisie Medicale [La]. 2010; 88 (7): 507-512
in French | IMEMR | ID: emr-134829

ABSTRACT

Composing of less than 1%of all ovarian cancers, immature teratoma is a malignancy that mainly affects the young. Immature teratoma of the ovary together with pregnancy is rare. To nor knowledge, this association was reported only in twelve cases. We Report two cases of immature teratoma of the ovary diagnosed during pregnancy and their respective issue. Observation 1st case. A 28 years old woman gravida 1 with an immature teratoma of the ovary discovered during delivery by caesarean section. The treatment was conservative including salpingo-oophorectomy, omentectomy. aortic lymph node dissection and appendectomy. This patient had a second pregnancy with a good outcome. She delivered by cacsarean section in order to perform radical treatment: hysterectomy and oophorectomy of the remaining ovary. 2nd case. A 22 years old woman gravida I with adnexal mass diagnosed during an ultrasonography exam at 15 weeks gestation. A conservative treatment was indicated, including salpingo oophorectomy, omentectomy, aortic lymph node dissection, appendectomy and biopsy of the resnaining ovary. The patient bad a normal vaginal delivery. Immature teratoma is graded from 1 to 3. The management of this association is discussed, but it takes in consideration the surgical staging, the grade and the secretion of alpha FP. Conservative treatment without associating chemotherapy can be tempted in tumours with a stade Al and a low grade


Subject(s)
Humans , Female , Teratoma/surgery , Ovarian Neoplasms/surgery , Pregnancy Complications, Neoplastic/diagnosis
2.
Neurosciences. 2004; 9 (1): 30-3
in English | IMEMR | ID: emr-67835

ABSTRACT

The aim of the study was to document the neuroimaging findings of children with infantile spasms [IS] seen over a 3-year period. All children below the age of 4 years who presented to the Pediatric Department at the Northern Area Armed Forces Hospital, Hafr Al-Batin, Kingdom of Saudi Arabia from January 1, 1998 to December 31, 2000 with a history of seizures, atypical movements, psychomotor delay, flexor, extensor spasms or both were included in the study. Relevant birth, developmental and family history as well as information on the pattern of fits were documented. Investigations included complete blood count, serum electrolytes, liver function tests, screening for acquired and congenital metabolic disorders. The electroencephalogram, brain magnetic resonance imaging and computerized tomography scans were carried out routinely on all the children. There were a total of 30 Saudi children, 17 males and 13 females that fulfilled the criteria for evaluation of infantile spasms. The mean age was 10 months. The major causes of IS in this study were congenital brain lesions [40%] infections [20%], and birth trauma/asphyxia [16.7%]. The etiology was unknown in 6 [20%] cases. The neuroimaging pattern was dysgenesis [30%], brain atrophy [23.7%], infarctions/hemorrhage [10%] and hydrocephaly [10%]. In 8 cases [26.6%] the findings were normal. The neuroimaging findings in this study are comparable with observations in other studies carried out under different clinical settings and environment


Subject(s)
Humans , Male , Female , Child , Tomography, X-Ray Computed , Magnetic Resonance Imaging , Electroencephalography , Spasms, Infantile/etiology
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