1.Two Cases of Fetal Giant Lymphangiomas.
Leek Bum CHON ; Sang Hee LEE ; Wee Hyun LEE
Korean Journal of Obstetrics and Gynecology 1999;42(10):2357-2361
In this paper, two unusual cases of fetal giant lymphangiomas diagnosed before delivery is reported in 18 and 26-week pregnant woman. They were diagnosed by ultrasound. Although the cause of lymphangioma is not clearly established, they probably arise from a failure of the developing lymphatic tissue to establish normal connection with the draining lymphatics. These anomalies are most often cervical (about 70~80%) but occasionally present in the axilla (about 10%), thorax and abdomen. Lymphangioma arising at posterior nuchal region is called cystic hygroma. Lymphangioma may be divided histologically into three types ; simple, cavernous or cystic. Ultrasound examination is essential method in prenatal diagnosis of fetal lymphangioma. The differential diagnosis of these fetal lymphangioma should include meningomyelocele, benign cystic teratoma, nuchal edema, encephalocele, and subchorial placenta cyst. About 60 to 70% of lymphangioma is accompanied with chromosomal abnormalities, and most common type is Turner's symdrome (40~80%), but occasionally trisomy 21, 18, 13 and 47 XXY. But chromosomal studies of these cases showed normal findings. The 26-week fetus was IUFD at 29 gestational weeks and terminated by hysterotomy. Other 18-week fetus was terminated by vaginal delivery after intrauterine decompression.
Abdomen
;
Axilla
;
Chromosome Aberrations
;
Decompression
;
Diagnosis, Differential
;
Down Syndrome
;
Edema
;
Encephalocele
;
Female
;
Fetus
;
Humans
;
Hysterotomy
;
Lymphangioma*
;
Lymphangioma, Cystic
;
Lymphoid Tissue
;
Meningomyelocele
;
Placenta
;
Pregnant Women
;
Prenatal Diagnosis
;
Teratoma
;
Thorax
;
Ultrasonography
2.A Case of Adenocarcinoma arising from a Mature Cystic Teratoma of the Ovary.
Leek Bum CHON ; Chan LEE ; Yong Hun CHEE ; Kye Won KWON ; Hee Jung AHN ; Jung Soo KIM
Korean Journal of Obstetrics and Gynecology 1997;40(10):2362-2366
Malignant transformation of mature cystic teratoma is a rare complication. Most com-mon malignant transformation of mature cystic teratoma is squamous cell carcinoma, which represents about 75 to 80% followed by adenocarcinoma in 6 to 7%. It is generally consi-dered that prognosis is extremely poor in case of adenocarcinoma associated with cystic te-ratoma. In this paper, we describe an adenocarcinoma arising from a mature cystic teratoma of left ovary in 47 year old woman. Left ovary was measured 18x15x7cm, 1,295gm in size. Uterus and right ovary were normal appearance. Left ovarian cyst was adhered to omentum and peritoneum. But neither rupture of cyst nor ascites were found at laparotomy. A brief review of concerned literatures was presented.
Adenocarcinoma*
;
Ascites
;
Carcinoma, Squamous Cell
;
Female
;
Humans
;
Laparotomy
;
Middle Aged
;
Omentum
;
Ovarian Cysts
;
Ovary*
;
Peritoneum
;
Prognosis
;
Rupture
;
Teratoma*
;
Uterus