1.Effects of ascorbate on the differentiation of B lymphocytes in sarcoma 180-implanted mice.
Young Jun KANG ; Jeong Hye ROH ; Sa Ouk KANG ; Ga Jin JEONG
Korean Journal of Immunology 1993;15(2):227-233
No abstract available.
Animals
;
B-Lymphocytes*
;
Mice*
;
Sarcoma*
2.Clinical significance of CA125 antigen levels in patients with adenomyosis and leiomyomata uteri.
Sa Jin KIM ; Jong Chul SHIN ; Jang Heub KIM ; Do Kang KIM
Korean Journal of Obstetrics and Gynecology 1991;34(2):253-257
No abstract available.
Adenomyosis*
;
Humans
;
Uterus*
3.Clinical significance of CA125 antigen levels in patients with adenomyosis and leiomyomata uteri.
Sa Jin KIM ; Jong Chul SHIN ; Jang Heub KIM ; Do Kang KIM
Korean Journal of Obstetrics and Gynecology 1991;34(2):253-257
No abstract available.
Adenomyosis*
;
Humans
;
Uterus*
4.Three Cases of Late Hemorrhagic Disease of Ingancy.
Yang Su KANG ; Ree Sa LEE ; Sang Kyn PARK ; Ho Jin PARK ; Mi Ja SHIN
Journal of the Korean Pediatric Society 1989;32(7):1001-1006
No abstract available.
5.One Case of Mucinous Ductal Ectasia Diagnosed with Ultrathin Pancreatoscopy.
Young Soo KIM ; Sung Won CHO ; Ki Baik HAHM ; Jin Hong KIM ; Sa Joon HONG ; Young Soo MOON ; Myung Ho YOON ; Han Keol KANG
Korean Journal of Gastrointestinal Endoscopy 1996;16(5):807-815
Mucinous ductal ectasia(MDE) is a newly described entity of mucinous neoplasm of pancreas with characteristic endoscopic and pancreatographic findings. It is charaeterized by a patulous duodenal papilla extruding mucus and a pancreatogram showing dilatation with amorphous filling defects, communication of the mass with the pancreatic duct. MDE is intraductal lesion consisting of dilated "cystified" ducts lined by mucin-producing columnar cells. The lesion is usually located in the head or uncinate process. When the radiographic appearance of the ERCP cannot provide sufficient information for definite diagnosis, additional endoscopic visualization is desirable. With the advent of pancreatoscopy, an endoscopic procedure is now available that has proven to enhance diagnostic accuracy. The 0.8-mm ultrathin pancreatoscope allows macroscopic diagnosis under direct vision. Endoscopic sphincterotomy is not required, and insertion into the pancreatic duct is feasible in most cases with the aid of guidewires. Major indications are unclear filling defects on ERCP, strictures of uncertain origin, and duct cut-offs. A limitation of this procedure are the lack of angulation, insufficient illumination, fragility of endoscopic equipment, and nonspecific findings. In addition, biopsy while directly viewing the lesion is impossible at present. We experienced one case of MDE who presented with the symptom of weight loss. Ultrathin pancreatoscopy was useful for the direct visualization af pancreatic duct in the differential diagnosis of filling defects of main pancreatic duct.
Biopsy
;
Cholangiopancreatography, Endoscopic Retrograde
;
Constriction, Pathologic
;
Diagnosis
;
Diagnosis, Differential
;
Dilatation
;
Dilatation, Pathologic*
;
Head
;
Lighting
;
Mucins*
;
Mucus
;
Pancreas
;
Pancreatic Ducts
;
Sphincterotomy, Endoscopic
;
Weight Loss
6.A Case of Retroperitoneal Teratoma Antenatally Diagnosed.
Mi Ji KANG ; Eun Jeong BAIK ; Jong Chul SHIN ; Hee Bong MOON ; Seung Hye RHO ; Sa Jin KIM ; Soo Pyung KIM
Korean Journal of Perinatology 2000;11(1):69-73
No abstract available.
Teratoma*
7.Two Cases of Congenital Atrichia Associated with the Gastrointestinal Anomaly in Siblings.
Jin Kyung JUNG ; Sang Ho BAIK ; Sa Young KIM ; Eui Tak OH ; Hong Ja KANG ; Kil Seo KIM
Journal of the Korean Pediatric Society 1996;39(9):1315-1319
Congenital atrichia is an anomaly characterized by congenital absence of hair in varying degrees as well as the ypopigmentation & poor development of the abnormal residual hair on the scalp, eyebrows, eyelashes & body. Two cases of congenital atrichia in siblings were reviewed. The first case was associated with congenital megacolon and skin biopsy of scalp (esp. parietal region) was non-specific. The second case was associated with bilateral inguinal hernia. Congenital atrichia is inherited by autosomal dominant or recessive. Acording to the limited pedigree data, our cases were X-linked recessive inheritance We report these cases with a review of related literatures.
Biopsy
;
Eyebrows
;
Eyelashes
;
Hair
;
Hernia, Inguinal
;
Hirschsprung Disease
;
Humans
;
Pedigree
;
Rabeprazole
;
Scalp
;
Siblings*
;
Skin
;
Wills
8.Two Cases of Congenital Atrichia Associated with the Gastrointestinal Anomaly in Siblings.
Jin Kyung JUNG ; Sang Ho BAIK ; Sa Young KIM ; Eui Tak OH ; Hong Ja KANG ; Kil Seo KIM
Journal of the Korean Pediatric Society 1996;39(9):1315-1319
Congenital atrichia is an anomaly characterized by congenital absence of hair in varying degrees as well as the ypopigmentation & poor development of the abnormal residual hair on the scalp, eyebrows, eyelashes & body. Two cases of congenital atrichia in siblings were reviewed. The first case was associated with congenital megacolon and skin biopsy of scalp (esp. parietal region) was non-specific. The second case was associated with bilateral inguinal hernia. Congenital atrichia is inherited by autosomal dominant or recessive. Acording to the limited pedigree data, our cases were X-linked recessive inheritance We report these cases with a review of related literatures.
Biopsy
;
Eyebrows
;
Eyelashes
;
Hair
;
Hernia, Inguinal
;
Hirschsprung Disease
;
Humans
;
Pedigree
;
Rabeprazole
;
Scalp
;
Siblings*
;
Skin
;
Wills
9.A Case of Giant Conjunctival Nevus Mimicking Malignant Melanoma.
Sa Kang KIM ; Hyuk Jin CHOI ; Mee Kum KIM ; Won Ryang WEE
Journal of the Korean Ophthalmological Society 2014;55(1):124-128
PURPOSE: We report a case of giant conjunctival nevus and compare differential diagnosis between giant conjunctival nevus and conjunctival malignant melanoma. CASE SUMMARY: A 46-year-old male presented with brown and elevated conjunctival mass in his right eye since childhood. The mass was located at the superior bulbar conjunctiva involving the superior cornea. The mass was 16 x 9 mm in size and elevated. Feeding vessels, intrinsic vessels and various cyst sizes were observed inside the mass. Resection of the conjunctival mass and amniotic membrane transplantation were performed. The histopathological diagnosis was conjunctival nevus. CONCLUSIONS: Conjunctival nevus is a benign conjunctival tumor with excellent prognosis, often confused with conjunctival melanoma. Both conjunctival nevus and conjunctival malignant melanoma are commonly located in the bulbar conjunctiva, pigmented and often have feeder and intrinsic vessels. Conjunctival nevus has an intralesional cyst, which is a key differentiating characteristic from malignant melanoma as many other features overlap. The change in tumor size, increased pigmentation and corneal invasion are features suspect of malignant transformation and surgical excision and histologic examination are recommended for those lesions. Surgical excision for giant conjunctival nevus can cause several ocular complications such as symblepharon. Conjunctival reconstruction with amniotic membrane transplantation is useful for preventing complications.
Amnion
;
Conjunctiva
;
Cornea
;
Diagnosis
;
Diagnosis, Differential
;
Humans
;
Male
;
Melanoma*
;
Middle Aged
;
Nevus*
;
Pigmentation
;
Prognosis
10.Transcervical expulsion of a submucosal myoma as a result of uterine artery embolization.
Jae Dong LEE ; Sa Jin KIM ; Hae Kyu LEE ; Jean A KIM ; Byung Chae KANG ; Soo Young HUR ; Gui Se Ra LEE ; Jong Chul SHIN ; Soo Pyung KIM
Korean Journal of Obstetrics and Gynecology 2000;43(2):318-321
Uterine artery embolization was introduced to arrest post-partum hemorrhage 20 years ago. It has also been used to control severe hemorrhage from uterine gestational trophoblast tumors, carcinoma of the uterus, uterine arteriovenous malformations, and cases of pelvic trauma. More recently, transcatheter uterine artery embolization is a new treatment for uterine leiomyoma. A 33-year old married woman with 2 children had a history of heavy pelvic pain and pressure. Ultrasound and MRI investigation showed a bulky 12 x 10cm submucosal myoma in right lower uterine segment. The both uterine artery embolization was performed via a bilateral femoral artery. We present a case in which successful embolization of the uterine arteries in a woman with submucosal myoma resulted in a subsequent transcervical expulsion of large pieces of the dominant fibroid after 3 month of treatment with a brief review.
Adult
;
Arteriovenous Malformations
;
Child
;
Female
;
Femoral Artery
;
Hemorrhage
;
Humans
;
Leiomyoma
;
Magnetic Resonance Imaging
;
Myoma*
;
Pelvic Pain
;
Trophoblastic Neoplasms
;
Ultrasonography
;
Uterine Artery Embolization*
;
Uterine Artery*
;
Uterus