1.A rare case of post-hysterectomy vault site iatrogenic endometriosis.
Cha Hien CHOI ; Jeong Jin KIM ; Woo Young KIM ; Kyeung Whan MIN ; Dong Hoon KIM
Obstetrics & Gynecology Science 2015;58(4):319-322
A 45-year-old woman with a prior history of hysterectomy due to adenomyosis and leiomyomas was presented at our outpatient gynecology clinic 13 months later with sudden lower pelvic discomfort and vaginal bleeding symptoms. The patient underwent vaginal vault biopsy however diagnosis was still uncertain. Additional evaluation was required due to massive rebleeding incidents. After an emergent explorative laparoscopic operation with total excision of the vault, a diagnosis of vaginal vault endometriosis was made. Our theory is that a possible transplantation of endometrial cells during morcellation of the adenomyotic uterus which then may have progressed to iatrogenic endometriosis of the vaginal vault. Therefore, vault endometriosis must be considered in incidences of delayed massive bleeding occurring in post-hysterectomy patients when other diagnoses have been excluded.
Adenomyosis
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Biopsy
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Diagnosis
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Endometriosis*
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Female
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Gynecology
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Hemorrhage
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Humans
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Hysterectomy
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Incidence
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Leiomyoma
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Middle Aged
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Outpatients
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Uterine Hemorrhage
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Uterus
2.Corticotropin-releasing Factor (CRF) and Urocortin Promote the Survival of Cultured Cerebellar GABAergic Neurons Through the Type 1 CRF Receptor.
Jae Sun CHOI ; Thao Thi Hien PHAM ; Yoon Jin JANG ; Bao Chi BUI ; Bong Hee LEE ; Kyeong Min JOO ; Choong Ik CHA ; Kyung Hoon LEE
Journal of Korean Medical Science 2006;21(3):518-526
Corticotropin releasing factor (CRF) is known to be involved in the stress response and in some degenerative brain disorders. In addition, CRF has a role as a neuromodulator in adult cerebellar circuits. Data from developmental studies suggest a putative role for CRF as a trophic factor during cerebellar development. In this study, we investigated the trophic role for CRF family of peptides by culturing cerebellar neurons in the presence of CRF, urocortin or urocortin II. Primary cell cultures of cerebella from embryonic day 18 mice were established, and cells were treated for either 1, 5 or 9 days with Basal Medium Eagles complete medium alone or complete medium with 1 micrometer CRF, urocortin, or urocortin II. The number of GABA-positive neurons in each treatment condition was counted at each culture age for monitoring the changes in neuronal survival. Treatment with 1 micrometer CRF or 1 micrometer urocortin increased the survival of GABAergic neurons at 6 days in vitro and 10 days in vitro, and this survival promoting effect was abolished by treatment with astressin in the presence of those peptides. Based on these data, we suggest that CRF or urocortin has a trophic role promoting the survival of cerebellar GABAergic neurons in cultures.
gamma-Aminobutyric Acid/*metabolism
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Time Factors
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Receptors, Corticotropin-Releasing Hormone/*metabolism
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Peptides/chemistry
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Neurons/*metabolism
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Mice, Inbred C57BL
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Mice
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Immunohistochemistry
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Image Processing, Computer-Assisted
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Corticotropin-Releasing Hormone/biosynthesis/*physiology
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Cerebellum/*embryology/*metabolism
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Cells, Cultured
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Cell Survival
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Animals