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1.
J Minim Invasive Gynecol ; 19(6): 775-9, 2012.
Article in English | MEDLINE | ID: mdl-23084686

ABSTRACT

We describe a conservative laparoscopic approach to treatment of a perforated pyomyoma after uterine artery embolization. A 36-year-old woman came to our emergency department 8 weeks after undergoing uterine artery embolization. She reported painful abdominal cramps. Physical examination revealed fever, tachycardia, hypotension, abdominal pain with rebound tenderness and pain during bimanual examination. Ultrasonography showed a fundal/subserosal leiomyoma and a moderate amount of fluid in the abdominal cavity. Because the patient desired preservation of the uterus, a laparoscopic approach was used for drainage and lavage of a perforated pyomyoma. The patient had an uneventful recovery and remained well at follow-up visits. Second-look diagnostic laparoscopy enabled treatment of the adhesions formed and revealed patent fallopian tubes. Surgery has been the primary approach to pyomyoma. However, hysterectomy leads to irreversible sterility and myomectomy can be difficult to perform. Therefore, there is need for a less invasive intervention in women who seek conservative treatment. Recently, computed tomography-guided drainage was successfully performed in two patients with pyomyoma. To our knowledge, this is the first report of a successful conservative laparoscopic approach to pyomyoma.


Subject(s)
Gram-Positive Bacterial Infections/therapy , Laparoscopy/methods , Leiomyoma/therapy , Uterine Neoplasms/therapy , Adult , Anti-Bacterial Agents/therapeutic use , Drainage , Female , Gram-Positive Bacterial Infections/complications , Humans , Leiomyoma/microbiology , Organ Sparing Treatments , Propionibacterium acnes , Therapeutic Irrigation , Uterine Artery Embolization/adverse effects , Uterine Neoplasms/microbiology
2.
J Obstet Gynaecol Res ; 38(2): 452-4, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22176344

ABSTRACT

A 16-year-old girl was referred to our center by her general physician because of primary amenorrhea. Her family history revealed an older sister with Swyer syndrome and gonadectomy at another institution. After thorough evaluation she received the same diagnosis, but unlike her sister, she refused gonadectomy. Four years later she presented with abdominal discomfort and a complex pelvic mass. She underwent exploratory laparotomy and histological examination revealed bilateral dysgerminoma without capsular invasion. The tumor was classified as stage IB. After surgery she underwent adjuvant chemotherapy with three cycles of BEP (bleomycin + etoposide + cisplatin). The present case emphasizes the importance of familial screening with a karyotype study in pure gonadal dysgenesis to prevent gonadal malignancy.


Subject(s)
Dysgerminoma/etiology , Gonadal Dysgenesis, 46,XY/complications , Ovarian Neoplasms/etiology , Adolescent , Dysgerminoma/therapy , Female , Gonadal Dysgenesis, 46,XY/genetics , Humans
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