1.The perinatal outcome of monoamniotic twin pregnancies.
Yun Sung JO ; Hyun Sun KO ; Dong Gyu JANG ; Youn Jin CHOI ; Hyen Ju SON ; Sa Jin KIM ; Jong Chul SHIN ; Guisera LEE
Korean Journal of Obstetrics and Gynecology 2010;53(10):881-887
OBJECTIVE: The purpose of this study was to determine the perinatal outcome in monoamniotic twin pregnancies and to review the recently published literature about the topic. METHODS: This retrospective study examined the records of prenatally diagnosed monoamniotic twin pregnancy casese in our institution between January 1997 and April 2010. RESULTS: Among 1,112 twin pregnancies, there were 15 (1.3%) monoamnionic twins, including 2 conjoined twin pregnancies. Twelve (80%), 9 (60%), 5 (33.3%), and 4 pregnancies (26.7%) delivered after 20, 30, 32, and 34 weeks, respectively. Among 12 pregnancies that continued after 20 weeks of gestation, three cases showed one-fetal death and one, both-fetal death. The perinatal mortality rate (from 20 weeks of gestation to 28 days after birth) was 37.5%. The incidence of lethal anomalies and congenital heart anomalies was 20% and 23.3%, respectively. The mean gestational age at delivery was 31.4+/-4.53 weeks; 16 of 18 neonates (84.2%) were admitted to the neonatal intensive care unit (NICU). Three neonates expired on the first day after birth. The mean duration of the NICU stays for 13 live neonates was 32.0+/-29.3 days (range, 3 to 114 days). The main causes of perinatal deaths were preterm birth, congenital anomalies, pregnancy loss before 20 weeks, and intrauterine fetal demise that might have resulted form cord entanglement. CONCLUSION: Perinatal mortality in monoamniotic twins was still very high and the survival rate after 32 weeks of gestation is approximately one-third. Further studies are needed to improve the perinatal mortality.
Gestational Age
;
Heart
;
Humans
;
Incidence
;
Infant, Newborn
;
Intensive Care, Neonatal
;
Parturition
;
Perinatal Mortality
;
Pregnancy
;
Pregnancy, Twin
;
Premature Birth
;
Retrospective Studies
;
Survival Rate
;
Twins
;
Twins, Conjoined
2.A Case of Thyroid MALT Lymphoma without Autoimmune Thyroiditis.
Ok Nyu KONG ; Sang Hyen JOO ; Sun Hye SHIN ; Min Ah NA ; Jun Hyeop AN ; Yang Ho KANG ; Do Youn PARK ; Seok Man SON ; In Ju KIM ; Yong Ki KIM
Journal of Korean Society of Endocrinology 2005;20(3):268-272
A primary thyroid lymphoma is rare among all types of thyroid malignancy. Usually, a thyroid lymphoma is associated with underlying chronic autoimmune thyroiditis. Recently, we experienced a primary thyroid mucosa-associated lymphoid tissue(MALT) lymphoma, with an incidental micropapillary thyroid carcinoma, but lacking evidence of autoimmune thyroiditis. A female patient visited our hospital for further evaluation of a rapidly enlarging, painless thyroid mass which had been stable for 8 years. Lymphocytic thyroiditis or a lymphoma was suspected from fine needle aspiration performed at another hospital. The thyroid function test and other routine laboratory tests were normal. The histopathological findings after a total thyroidectomy revealed a MALT lymphoma with a micropapillary thyroid carcinoma. There was no evidence of chronic autoimmune thyroiditis. This is, to the best of our knowledge, the first case report of a MALT lymphoma arising from the thyroid gland without evidence of chronic autoimmune thyroiditis in Korea
Biopsy, Fine-Needle
;
Female
;
Humans
;
Korea
;
Lymphoma
;
Lymphoma, B-Cell, Marginal Zone*
;
Thyroid Function Tests
;
Thyroid Gland*
;
Thyroid Neoplasms
;
Thyroidectomy
;
Thyroiditis, Autoimmune*
3.A Case of Thyroid MALT Lymphoma without Autoimmune Thyroiditis.
Ok Nyu KONG ; Sang Hyen JOO ; Sun Hye SHIN ; Min Ah NA ; Jun Hyeop AN ; Yang Ho KANG ; Do Youn PARK ; Seok Man SON ; In Ju KIM ; Yong Ki KIM
Journal of Korean Society of Endocrinology 2005;20(3):268-272
A primary thyroid lymphoma is rare among all types of thyroid malignancy. Usually, a thyroid lymphoma is associated with underlying chronic autoimmune thyroiditis. Recently, we experienced a primary thyroid mucosa-associated lymphoid tissue(MALT) lymphoma, with an incidental micropapillary thyroid carcinoma, but lacking evidence of autoimmune thyroiditis. A female patient visited our hospital for further evaluation of a rapidly enlarging, painless thyroid mass which had been stable for 8 years. Lymphocytic thyroiditis or a lymphoma was suspected from fine needle aspiration performed at another hospital. The thyroid function test and other routine laboratory tests were normal. The histopathological findings after a total thyroidectomy revealed a MALT lymphoma with a micropapillary thyroid carcinoma. There was no evidence of chronic autoimmune thyroiditis. This is, to the best of our knowledge, the first case report of a MALT lymphoma arising from the thyroid gland without evidence of chronic autoimmune thyroiditis in Korea
Biopsy, Fine-Needle
;
Female
;
Humans
;
Korea
;
Lymphoma
;
Lymphoma, B-Cell, Marginal Zone*
;
Thyroid Function Tests
;
Thyroid Gland*
;
Thyroid Neoplasms
;
Thyroidectomy
;
Thyroiditis, Autoimmune*