A 14 years old woman with a giant mucinous adenocarcinoma of the ovary

The diagnosis of ovarian tumor in pediatrics is often difficult and delayed due to unspecific call signs and polymorphic imaging presentations. These tumors are rare, estimated in children at around 2.6 / 100,000 girls per year, functional lesions being excluded. Ten to 20% of them are malignant [1-2] and represent 3% of cancers in girls under the age of 15 [3]. The World Health Organization classifies these tumors into three main groups based on whether they are derived from the surface epithelium, germline cells or ovarian stroma or sex cords. Primary or secondary locations are possible in leukemias and lymphomas [4-5]. Giant ovarian cystadenocarcinomas are rarely described. The huge ovarian masses are mostly benign, but the malignancy should be ruled out by pathology exams. Giant cysts require resection by laparotomy because of compression symptoms or the risk of malignancy, but also to prevent perforation and spillage of cystic fluid into the peritoneal cavity [6]. Here we report an observation made in a 14-year-old girl who was diagnosed with a large ovarian tumor and who was found to be a malignant tumor on pathology with papillary-type mucinous cystadenocarcinoma.</jats:p

Management of placenta percreta. A case report

The placenta accreta designates an abnormality of the placental insertion characterized, on the anatomopathological level, by an absence of deciduous deciduous between the placenta and the myometrium. This insertion anomaly may interest all or only part of the placenta. We distinguish within this terminology the terms of - placenta accreta when the placenta is simply attached to the Myometrium. - placenta increta when the placenta invades the myometrium. - placenta percreta when the placenta enters the serosa uterine, or even the neighboring organs (bladder, peritoneum, etc.) [1]. Placentas accretas are a high-risk situation for severe postpartum hemorrhage and its inherent complications such as disseminated intravascular coagulation, hemostasis hysterectomy, surgical wounds to the ureters, bladder, multiple organ failure, or even maternal death, particularly in the case of placenta percreta [2,3]. Risk factors for placenta percreta include a history of cesarean, uterine curettage or manual removal of placenta, presence of placenta previa, endometriosis, high parity and advanced maternal age [4]. We report the case of a 30-year-old woman, IIGIIP, who had a previous cesarean section during her first pregnancy and who had a placenta percreta and who underwent hysterectomy without cystectomy and without ligation of the hypogastric arteries.</jats:p

Peritonitis by Spontaneous rupture of ovarian dermoid cyst: a case report

Background: Ovarian dermoid cyst is a benign congenital tumor. It is often incidentally diagnosed and can be revealed in very rare cases by spontaneous rupture. We report the case of a ruptured ovarian dermal cyst complicated by generalized peritonitis. Case report: This was a 20-year-old female patient, who consulted for abdominal pain associated with fever and vomiting. Physical examination found generalized abdominal contracture. Plain abdominal radiography found pneumoperitoneum. Biology showed leukocytosis at 18000 / mm3. Median laparotomy revealed a collection 2000 cc of pus with a ruptured right ovarian mass. An adnexectomy with lavage of abdominal cavity were performed. Anatomopathological examination concluded to an ovarian dermoid cyst with no sign of malignancy. The postoperative course was uneventful. Conclusion: Rupture of a dermoid cyst of the ovary is a rare acute complication. Examination of the operative specimen is mandatory to eliminate malignancy. Keywords: Ovary; Dermoid cyst; Rupture; Acute complication; Peritonitis; Ovary</jats:p