1.Factors affecting the satisfaction rate of radiofrequency myolysis: 18 months follow up.
Hyun Hee CHO ; Jae Eun CHUNG ; Sung Jin HWANG ; In Cheul JEUNG ; Sue Yeon KIM ; Mee Ran KIM ; Jang Hub KIM ; Jin Hong KIM
Korean Journal of Obstetrics and Gynecology 2007;50(11):1508-1514
OBJECTIVE: To report 18 months follow up results of radiofrequency myolysis and analysis the factors which effect the success rate of myolysis. METHODS: 153 patients who took radiofrequency myolysis between October 2004.~June 2006 in this hospital were enrolled this retrospective study. Except 14 patients which had incomplete data, total 139 patient's charts were reviewed. Sonographic evaluations were checked after a week, 1 month, 3 months, 6 months, 12 months, and 18 months after myolysis. Questions about complications like vaginal bleeding, abdominal pain, feber and vaginal discharge were asked to patients in every visits. Volume of the myoma were checked via 3D ultrasonography. RESULTS: Reduction rate of the volume of myoma after 18 months were 73% and reoperation rate were 4.3%. Improvement rates of patients symptom were 87% (menorrhagea 95%, dysmenorrheal 75%, pelvic pain 60%) The patients who had myomas sized over 100 ml before treatments showed statistically higher rate of reoperation, and decreased rate of satisfaction. Reoperation rate and reduction rate of myoma showed no difference through pathologic diagnosis. The patients who had initial symptoms showed higher rate of satisfaction after myolysis. Total satisfaction rate were 62%, and no serious complications like bowel injury, bladder injury, sepsis and peritonitis were not reported. CONCLUSION: Satisfaction rate after radiofrequency myolysis was increased in symptomatic leiomyoma especially smaller than 6.5 cm in diameter.
Abdominal Pain
;
Diagnosis
;
Follow-Up Studies*
;
Humans
;
Leiomyoma
;
Myoma
;
Pelvic Pain
;
Peritonitis
;
Reoperation
;
Retrospective Studies
;
Sepsis
;
Ultrasonography
;
Urinary Bladder
;
Uterine Hemorrhage
;
Vaginal Discharge
2.Cohort Infant Mortality Rate of Gunwee and Hapchun Counties and an MCH Center in Taegu.
Jung Han PARK ; Min Hae YEH ; Byung Yeol CHUN ; Sung Euk CHO ; Hyun KIM ; Han Jin CHUNG ; Jae Yeon CHO ; Jung Hub SONG ; Gui Yeon KIM ; Jang Rak KIM
Korean Journal of Preventive Medicine 1990;23(1):87-97
No abstract available.
Cohort Studies*
;
Daegu*
;
Humans
;
Infant
;
Infant Mortality*
;
Infant*
3.Transient lysosomal activation is essential for p75 nerve growth factor receptor expression in myelinated Schwann cells during Wallerian degeneration.
Junyang JUNG ; Wenting CAI ; So Young JANG ; Yoon Kyoung SHIN ; Duk Joon SUH ; Jong Kuk KIM ; Hwan Tae PARK
Anatomy & Cell Biology 2011;44(1):41-49
Myelinated Schwann cells in the peripheral nervous system express the p75 nerve growth factor receptor (p75NGFR) as a consequence of Schwann cell dedifferentiation during Wallerian degeneration. p75NGFR has been implicated in the remyelination of regenerating nerves. Although many studies have shown various mechanisms underlying Schwann cell dedifferentiation, the molecular mechanism contributing to the re-expression of p75NGFR in differentiated Schwann cells is largely unknown. In the present study, we found that lysosomes were transiently activated in Schwann cells after nerve injury and that the inhibition of lysosomal activation by chloroquine or lysosomal acidification inhibitors prevented p75NGFR expression at the mRNA transcriptional level in an ex vivo Wallerian degeneration model. Lysosomal acidification inhibitors suppressed demyelination, but not axonal degeneration, thereby suggesting that demyelination mediated by lysosomes may be an important signal for inducing p75NGFR expression. Tumor necrosis factor-alpha (TNF-alpha) has been suggested to be involved in regulating p75NGFR expression in Schwann cells. In this study, we found that removing TNF-alpha in vivo did not significantly suppress the induction of both lysosomes and p75NGFR. Thus, these findings suggest that lysosomal activation is tightly correlated with the induction of p75NGFR in demyelinating Schwann cells during Wallerian degeneration.
Axons
;
Cell Dedifferentiation
;
Chloroquine
;
Demyelinating Diseases
;
Lysosomes
;
Myelin Sheath
;
Nerve Growth Factor
;
Peripheral Nervous System
;
RNA, Messenger
;
Schwann Cells
;
Tumor Necrosis Factor-alpha
;
Wallerian Degeneration