1.Tumor Angiogenesis and Vascular Endothelial Growth Factor Expression in Cervical Intraepithelial Neoplasia.
Hye Jean PARK ; Hye Jin PARK ; Hye Sung MOON ; Woon Sup HAN ; Sun Hee SUNG
Korean Journal of Pathology 2000;34(7):524-530
Angiogenesis is an essential requirement for development, progression, and metastasis of malignant tumors. Vascular endothelial growth factor (VEGF) is one of the important angiogenic factors. Recently the role of angiogenesis has been known in premalignant lesions. This study was performed to determine whether the angiogenesis and VEGF expression were increased in association with histological grade of cervical intraepithelial neoplasia (CIN) and to see the relationship between the angiogenesis and VEGF. Immunostainings for factor VIII and VEGF were performed on 52 cases of cervical neoplasia (12 cases of CIN I, 11 cases of CIN II, 15 cases of CIN III, 7 cases of microinvasive squamous cell carcinoma, and 7 cases of invasive carcinoma) and 5 cases of normal cervix. The results showed a significant increase of microvessel count from normal cervix through CIN grades to invasive squamous cell cacinoma. VEGF expression was increased in proportion to the CIN grades. There was no significant correlation between microvessel count and VEGF expression. In conclusion, the tumor angiogenesis is an early event in tumorigenesis of uterine cervix. In addition, no significant relationship between the microvessel count and VEGF expression in CIN suggests the possibility of other growth factors affecting mainly angiogenesis of premalignant lesion of uterine cervix.
Angiogenesis Inducing Agents
;
Carcinogenesis
;
Carcinoma, Squamous Cell
;
Cervical Intraepithelial Neoplasia*
;
Cervix Uteri
;
Factor VIII
;
Female
;
Intercellular Signaling Peptides and Proteins
;
Microvessels
;
Neoplasm Metastasis
;
Vascular Endothelial Growth Factor A*
2.Two Cases of Kallmann Syndrome.
Hye Jung HAN ; Hee Jin CHO ; Hye Sun LEE ; In Sil LEE ; Il Tae HWANG
Journal of Korean Society of Pediatric Endocrinology 2003;8(2):179-183
Kallmann syndrome is characterized by hypogonadotropic hypogonadism resulting from insufficient release of GnRH and associated with anosmia or hyposmia. We experienced two cases of Kallmann syndrome with abnormal brain MRI findings(olfactory bulb aplasia) & secondary sexual dysfunction.
Brain
;
Gonadotropin-Releasing Hormone
;
Hypogonadism
;
Kallmann Syndrome*
;
Magnetic Resonance Imaging
;
Olfaction Disorders
3.Two Cases of Kallmann Syndrome.
Hye Jung HAN ; Hee Jin CHO ; Hye Sun LEE ; In Sil LEE ; Il Tae HWANG
Journal of Korean Society of Pediatric Endocrinology 2003;8(2):179-183
Kallmann syndrome is characterized by hypogonadotropic hypogonadism resulting from insufficient release of GnRH and associated with anosmia or hyposmia. We experienced two cases of Kallmann syndrome with abnormal brain MRI findings(olfactory bulb aplasia) & secondary sexual dysfunction.
Brain
;
Gonadotropin-Releasing Hormone
;
Hypogonadism
;
Kallmann Syndrome*
;
Magnetic Resonance Imaging
;
Olfaction Disorders
4.Transarterial chemoembolization through collateral vessels in hepatocellular carcinoma.
Ji Hye KIM ; Joon Koo HAN ; Jin Wook CHUNG ; Jae Hyung PARK ; Man Chung HAN
Journal of the Korean Radiological Society 1993;29(6):1220-1228
We performed 70 proceudres of transarterial chemoembolization (TAE) through extrahepatic collateral vessels (n=27) or parasitic feeders (n=18) in 45 hepatocellular carcinoma patients. The collaterals developed after interruption of the hapatic artery due to repeated TAE(n=17), surgical ligation(n=7) and primary celiac occlusion (n=3). Radiologic findings suggesting the existence of parasitic or collateral supply for hepatocellular carcinoma were 1) a focal defect of Lipiodol retention on CT or plain film after TAE via the hepatic artery, 2) dilated and tortuous vessels around the mass on angiography, 3) persistent elevation of the level of serum alpha fetoprotein or continuous clinical symptoms in spite of sufficient devascularization of the tumor via the hepatic artery, and 4) radiological findings of direct invasion into adjacent organ. The sites of the catheter placement were the inferior phrenic artery (n=19), omental branches (n=16), periportal collaterals (n=6), pancreaticodenal arcade (n=3), gastroduodenal artery (n=3), internal mammary artery (n=2), intercostal artery (n=2), lateral thoracic artery (n=1), bronchial artery(n=1), and colic branches(n=1). Masses feeded by the inferior phrenic and chest wall collaterals were usually located at the dome area of the liver, and the omental and gastroduodenal collaterals developed in the masses located at the inferior tip of the liver. After TAE via collateral vessels, 37 patients underwent follow-up study. In 18 cases(48%), the tumor favorably responded to TAE. Specific complications of collateral TAE were epigastric soreness (n=10), severe shoulder pain (n=4), and embolization of the spinal artery during embolization through the intercostal artey (n=1). In conclusion, various extrahepatic collaterals are important alternative or additional routes for effective chemoembolization in patients with advanced hepatoma, and early recognition of the parasitic supply and the effort to perform TAE via collaterals is very important for effective management of the patients with the hepatoma.
alpha-Fetoproteins
;
Angiography
;
Arteries
;
Carcinoma, Hepatocellular*
;
Catheters
;
Colic
;
Ethiodized Oil
;
Follow-Up Studies
;
Hepatic Artery
;
Humans
;
Liver
;
Mammary Arteries
;
Shoulder Pain
;
Thoracic Arteries
;
Thoracic Wall
5.Management of Fournier's Gangrene with PGE1 and Bilateral Superomedial Thigh Flap.
Hye June PARK ; Dong Jin LEE ; Jin Han CHA ; Yang Woo KIM
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1999;26(5):1077-1081
Fournier's gangrene is an infective necrotizing fasciitis of the perineal, genital or perianal regions. Management of this disease has involved prompt surgical debridement with initiation of broad spectrum antibiotics and intensive supportive care. Multiple debridements orchiectomy, urinary deversion, and fecal diversion should be performed as clinically indicated. Hyperbaric oxygen therapy and topical application of unprocessed honey may prove to be useful adjuncts as new therapies. After excision of all necrotic tissue, the tissue losses have been managed by primary repair. split-thickness skin grafts, rotational or free myocutaneous flaps and omental flaps. Skin graft did not take on bare testis lacking the tunica vaginalis, and gracilis myocutanous flap was too bulky to cover the scrotal area. The progress of necrosis ceased by using intravenous PGE1 injection in the aspect of characteristic obliterative endarteritis causing cutaneous and subcutaneous vascular thrombosis and necrosis of tissue in Fournier's gangrene. We have reconstructed large scrotal defects with bilateral superomedial thigh flap in three Fournier's gangrene patients after stopping tissue necrosis with PEG1 treatment and several surgical debridements of the wounds. The use of this flap ensures a virtually normal sensation, which is important for the erotic propensity of the scrotum. Easy flap design and dissection, as well as primary closure of the donor site, are another benefits of this method.
Alprostadil*
;
Anti-Bacterial Agents
;
Debridement
;
Endarteritis
;
Fasciitis, Necrotizing
;
Fournier Gangrene*
;
Honey
;
Humans
;
Hyperbaric Oxygenation
;
Myocutaneous Flap
;
Necrosis
;
Orchiectomy
;
Scrotum
;
Sensation
;
Skin
;
Testis
;
Thigh*
;
Thrombosis
;
Tissue Donors
;
Transplants
;
Wounds and Injuries
6.Genetic Analysis in a Case of Transient Neonatal Diabetes Mellitus with Congenital Adrenal Hyperplasia.
Hye Jin KWON ; Jin A PARK ; Sang Lack LEE ; Heung Sik KIM ; Dong Seok JEON ; Dong Kyu JIN ; Pyoung Han HWANG
Journal of Korean Society of Pediatric Endocrinology 2002;7(1):116-121
A case of transient neonatal diabetes mellitus combined with congenital adrenal hyperplasia(CAH) is described. A female infant was born by cesarean delivery due to fetal distress, she had sunken eyeball and anterior fontanelle, large protruded tongue and thin subcutaneous tissues. She had large clitoris and progressive pigmentation on whole body was observed since 10th day of birth. Hyperglycemia and glycosuria was noted at 3rd day of birth. Level of insulin and C-peptide was 3.0 mU/L and 0.35 ng/mL respectively. Serum ACTH was 870.4 pg/mL and 17-hydroxyprogesterone was increased to 20,000 ng/dL. Serum Na was 124 mEq/L, K 5.6 mEq/L. Abdominal MRI showed no abnormality. Chromosomal study showed 46,XX. Genetic analysis with polymorphic DNA markers for chromosome 6 showed paternal uniparental isodisomy at D6S276, D6S1704 and DNA analysis of CYP 21 gene showed mutation at P435S. She required insulin therapy for 8 months after birth. Hydrocortisone and florinef was needed for the control of CAH.
17-alpha-Hydroxyprogesterone
;
Adrenal Hyperplasia, Congenital*
;
Adrenocorticotropic Hormone
;
C-Peptide
;
Chromosomes, Human, Pair 6
;
Clitoris
;
Cranial Fontanelles
;
Diabetes Mellitus*
;
DNA
;
Female
;
Fetal Distress
;
Genetic Markers
;
Glycosuria
;
Humans
;
Hydrocortisone
;
Hyperglycemia
;
Infant
;
Insulin
;
Magnetic Resonance Imaging
;
Parturition
;
Pigmentation
;
Subcutaneous Tissue
;
Tongue
;
Uniparental Disomy
7.Translocation of p53 Protein in Melanocytes and Malignant Melanoma Cells After UVB Irradiation.
Kyoung Hee CHOI ; Hye Jin KIM ; Yong CHOI ; Kyu Han KIM ; Kyoung Chan PARK
Annals of Dermatology 2001;13(3):133-138
BACKGROUND: UVB is responsible for most of the carcinogenic effects of sun exposure. OBJECTIVE: Aim of this study was to investigate the regulation and intracellular redistribution of p53 protein after UVB irradiation. METHODS: Cultured normal human melanocytes and G361 melanoma cells were used for west-ern blotting and confocal microscopic examination for determining expression and distribution of p53. RESULTS: UVB irradiation increased p53 expression in cultured normal human melanocytes and G361 malignant melanoma cells according to increasing doses of UVB. Furthermore, p53 moved from cytosol to nucleus after UVB irradiation. CONCLUSIONS: UVB irradiation induced overexpression and redistribution of p53 in cultured normal human melanocytes and G361 malignant melanoma cells.
Cytosol
;
Humans
;
Melanocytes*
;
Melanoma*
;
Solar System
8.A Case of Pyogenic Liver Abscess Caused by Staphylococcus epidermidis in a Healthy Child.
Ji Hye GWAK ; Yeun Joo EEM ; Ui Yoon CHOI ; Jin Han KANG
Korean Journal of Pediatric Infectious Diseases 2013;20(1):36-40
Staphylococcus epidermidis is a normal inhabitant of skin, throat, mouth, vagina, and urethra. It is not usually pathogenic, particularly in immunocompetent hosts. This report describes a case of a pyogenic liver abscess caused by Staphylococcus epidermidis in a healthy 12-year-old boy. He was admitted to Seoul St. Mary's Hospital with intermittent fever for 6 days. Findings on abdominal computed tomography (CT) showed a mass measuring 7.0x6.5 cm in the right hepatic lobe. Culture of the abscess resulted in growth of Staphylococcus epidermidis as a causative organism. The patient was successfully treated with intravenous administration of antibiotics and percutaneous drainage of the abscess.
Abscess
;
Administration, Intravenous
;
Anti-Bacterial Agents
;
Child
;
Drainage
;
Fever
;
Humans
;
Liver Abscess
;
Liver Abscess, Pyogenic
;
Mouth
;
Pharynx
;
Skin
;
Staphylococcus
;
Staphylococcus epidermidis
;
Urethra
;
Vagina
9.Sertoli-Leydig Cell Tumor of Hemangiopericytoma Pattern: A case report.
Hye Jin LEE ; Young im HAN ; Hyeon Ok KIM ; Kang Suek SUH ; Sun Kyung LEE
Korean Journal of Pathology 1995;29(6):815-818
The Sertoli-Leydig cell tumor is a gonadal tumor of sex-cord stromal type, similar to that seen in of the various phases of testicular development in the male. This tumor is exceedingly rare, accounting for only 0.1% to 0.5% of all primary ovarian neoplasms. It occurs predominantly in the second and third decades(mean age about 25 years), less than 10% after menopause. We investigated a case of poorly differentiated Sertoli-Leydig cell tumor of right ovary, occured in a 76-year-old woman. Grossly, the tumor measured 2, 100 gm in weight and 25 x 19 x 8 cm in dimensions. The outer surface was smooth and glistening without rupture of the capsule. Cut sections revealed a multilobulated brown solid mass with multiple cystic change. Microscopically, it showed the typical findings o a Sertoli-Leydig cell tumor. The characteristic feature is hemangiopericytoma paftem of sarcomatoid spindle cells. Therefore, we present it with a brief review of the literature.
Female
;
Humans
10.Malignant Small Cell Tumor of the Thoracopulmonary Region (Askin Tumor): Report of a case.
Young Im HAN ; Hye Jin LEE ; Kang Suek SUH ; Sun Kyung LEE
Korean Journal of Pathology 1995;29(5):687-690
Malignant small cell tumor(MSCT) of the thoracopulmonary region(Askin tumor) is extremely rare and is seen predominantly in children and adolescents. This tumor represents a distinct clinicopathologic entity of neuroectodertnal origin, arising from the soft tissues of the chest wall or peripheral lung. This tumor tends to recur locally, but does not seem to disseminate widely. The overall survival is poor. Recently, we experienced a case of the MSCT of the thoracopulmonary region of a 12-year-old female. She was admitted because of a chest wall mass on radiographic examination, and a complaint of intermittent chest pain. Grossly, the mass was lobulated, round and had a solid appearance with focal necrosis and hemorrhage on the cut surface. Histologically, small round to oval cells were arranged in compact sheets, nests and lobular patterns with intervening fibrovascular stroma. Ultrastructurally, the presence of loose-fitting membrane-bound neurosecretory granules was noted.
Child
;
Adolescent
;
Male
;
Female
;
Humans