1.Factors Affecting on the Invasiveness of the Prostate Cancer Cell on In Vitro Model of Basement Membrane.
Jae Seog HYUN ; Hyun LEE ; Jong Yoon BAHK
Korean Journal of Urology 1996;37(10):1057-1066
This study was aimed to examine whether biological characteristics of the cancer cell lines have any correlation with distinctive movement of the reconstituted basement membrane in modified Boyden chamber. The in vitro model consists of a chamber and basement membrane filter. Matrigel was applied on the upper surface of the filter and type IV collagen, fibronectin and laminin were also applied to the lower surface of the filter, respectively. The cancer invasiveness was measured by the number of the moved cells through basement membrane differing in component, thickness and incubation time. For chemoattractant study, serum free medium, medium supplemented with 10% fetal bovine serum and medium supplemented with 10% fetal bovine serum and 0.1% bovine serum albumin were used. The invaded cancer cells were counted under high-power field microscope and the morphologic feature of invading cancer cells on reconstituted basement membrane was examined with scanning electron microscopy. The effects of the tissue inhibitor of metalloproteinase-2 (TIMP-2) and wild type tumor necrosis factor-alpha (wTNF-a) on invasiveness of three prostate cancer cell lines (hormone intermediate sensitive ALVA 101, and hormone refractory ALVA 41 and PPC-1) were investigated. The rate of movement of the cancer was reduced increasing thickness of the matrigel but increased in proportion to the incubation time (p<0.05). The components applied on the lower surface of the filter did not affect cancer cell invasiveness (p>0.05). TIMP-2 reduced the invasiveness of three kinds of cancer cell line at both the high and low concentration, indicating that this agent interferes the movement of the cells. Furthermore, this result suggests that TIMP-2 might repress metal-dependent enzymes, which are thought to elicit the invasiveness of the cancer cells. The wTNF-a did not show any effects on the invasiveness of three cell lines. The additive chemoattractant effect of 0.1% bovine serum albumin was not observed and serum free medium also did not induce the cancer cell invasion across the reconstituted basement membrane. The migration of the ALVA 41 and PPC-1 were more than the ALVA 101. The scanning electron microscopic examination showed the figures of migration of cancer cells through the pores on filter, supporting our experiments are performed in validness. The effect of protease inhibitor was distinct in different cancer cell lines studied. From this experiment, we conclude that the rate of movement of both ALVA 41 and PPC-1 cells with shorter doubling time and the hormone refractory was faster than that of ALVA 101 cells with longer doubling time and the hormone sensitive, suggesting biological characteristics of the cells are implicated in degree of cancer cell invasiveness and their malignancies.
Basement Membrane*
;
Cell Line
;
Collagen Type IV
;
Fibronectins
;
Laminin
;
Microscopy, Electron, Scanning
;
Population Characteristics
;
Prostate*
;
Prostatic Neoplasms*
;
Protease Inhibitors
;
Serum Albumin, Bovine
;
Tissue Inhibitor of Metalloproteinase-2
;
Tumor Necrosis Factor-alpha
2.A Case of Calciphylaxsis.
Hyun Seung LEE ; Kwang Hyun CHO ; Dae Seog HEO ; Jai Kyoung KOH
Korean Journal of Dermatology 1999;37(1):87-90
Calciphylaxsis is a rare and life-threatening condition of progressive cutaneous necrosis secondary to calcification of small and medium-sized blood vessels. It is seen almost exclusively in patients with end-stage renal disease, in a setting of secondary hyperparathyroidism and hypercalcemia resulting in metastatic vascular calcification, We experienced a case of calciphylaxsis manifested with chara- cteristic cutaneous lesions that began as tender violaceous livedoid discolorations and subsequent ulceration on the proximal aspect of the extremities and on the lower part of the abdomen. Histologically, calcification is found in small and medium-sized blood vessels in the deep dermis and subcutaneous tissue. The patient had been treated for hypercalcemia, not complicating renal failure, but the cause of hypercalcemia was not found. However, the hypercalcemia was contolled and the skin lesions also improved after oral prednisolone therapy. Our case is a rare presentation of calciphylaxsis in the absence of renal failure, reversibly improved.
Abdomen
;
Blood Vessels
;
Dermis
;
Extremities
;
Humans
;
Hypercalcemia
;
Hyperparathyroidism, Secondary
;
Kidney Failure, Chronic
;
Necrosis
;
Prednisolone
;
Renal Insufficiency
;
Skin
;
Subcutaneous Tissue
;
Ulcer
;
Vascular Calcification
3.A Case of Erythema Multiforme Associated with Malignant Lymphoma.
Un Cheol YEO ; Kwang Hyun CHO ; Yoo Shin LEE ; Dae Seog HEO ; Seung Chul LEE
Korean Journal of Dermatology 1990;28(5):597-601
No abstract available.
Erythema Multiforme*
;
Erythema*
;
Lymphoma*
4.A Case of Apocrine Poroma.
Hyun Jeong LEE ; Seog Jun HA ; Sang Jung LEE ; Jin Wou KIM
Annals of Dermatology 2000;12(1):60-63
Apocrine poroma is a benign cutaneous adnexal neoplasm differentiating in the direction of sebaceous and apocrine glands, and follicular germs. The clinical appearance of apocrine poroma is not distinctive, and the histologic finding is similar to that of eccrine poroma, which is typified by proliferation of poroid and luminal cells in continuity with the epidermis. But sebaceous, apocrine or follicular differentiation may also be found in the case of apocrine poroma. We herein report a case of apocrine poroma on the scalp. This case exhibited apocrine and sebaceous differentiation, and connection to an adjacent follicular epithelium.
Apocrine Glands
;
Epidermis
;
Epithelium
;
Phenobarbital
;
Poroma*
;
Scalp
5.A Case of Tubular Apocrine Adenoma.
Hyun Jeong LEE ; Kee Young ROH ; Seog Jun HA ; Seok Jin KANG ; Jin Wou KIM
Annals of Dermatology 1999;11(4):297-299
Tubular apocrine adenoma is a well-circumscribed intradermal benign tumor with tubular structures showing apocrine differentiation. Most of those cases occur on the scalp in middle aged women. Histologically, tubular structure with apparent apocrine decapitation secretion, cystic dilatation of tubule, and connection with epidermis are the characteristic features of tubular apocrine adenoma. We presented a case of tubular apocrine adenoma that had recurred after incomplete excision. It showed apocrine decapitation secretion histologically and both eccrine and apocrine differentiation on immunohistochemical study.
Adenoma*
;
Decapitation
;
Dilatation
;
Epidermis
;
Female
;
Humans
;
Middle Aged
;
Scalp
6.Late Onset Ota Nevus.
Hyun Jeong LEE ; Kee Young ROH ; Seog Jun HA ; Jin Wou KIM
Annals of Dermatology 1999;11(4):289-291
Ota nevus is a dermal melanocytic harmatoma derived from neural crest melanoblast and involves skin innervated by the trigeminal nerve. Although most cases are clinically apparent at birth or around puberty, acquired lesions in adults have been rarely reported. We reported a 73 year-old Korean man with Ota nevus of the face and scalp that onset in his eighth decade and accompanied multiple solar comedo of the face.
Adolescent
;
Adult
;
Humans
;
Neural Crest
;
Nevus of Ota*
;
Parturition
;
Puberty
;
Scalp
;
Skin
;
Trigeminal Nerve
7.A Case of Isolated Plexiform Neurofibroma.
Hyun Jeong LEE ; Bo Kyung KOH ; Seog Jun HA ; Jin Wou KIM
Annals of Dermatology 2000;12(4):271-274
Plexiform neurofibroma is considered to be pathognomic of neurofibromatosis type 1 (NF1). Herein we report a solitary plexiform neurofibroma which is not associated with NF1. A 61-year-old man presented with asymptomatic skin colored nodules on the medial side of his left great toe. No other abnormalities were found in his personal or family history. Clinically, the tumor was simulating the appearance of mucous cysts. Microscopically,it was a plexiform neurofibroma located in the dermis which seemed to originate from small superficial nerves. This case would seem to confirm that the superficial form of plexiform neurofibroma involving small nerves in the dermis or subcutis is not necessarily pathognomic for NF1.
Dermis
;
Humans
;
Middle Aged
;
Neurofibroma, Plexiform*
;
Neurofibromatosis 1
;
Skin
;
Toes
8.A Case of Pigmented Bowen's Disease.
Hyun Jeong LEE ; Shin Taek OH ; Seog Jun HA ; Jin Wou KIM
Annals of Dermatology 2000;12(1):68-70
A 38-year-old woman was presented with a dark brown plaque on the abdomen. Clinically, the tumor was simulating the appearance of dysplastic nevus. Microscopically, the cells of the stratum malphighii lay in a disordered pattern. Many cells in the epidermis were atypical and melanin pigment was mainly in the basal layer of the epidermis and the upper dermis. Diagnosis of pigmented Bowen's disease was made. Pigmented Bowen's disease is rarely found at body sites other than the anogenital area.
Abdomen
;
Adult
;
Bowen's Disease*
;
Dermis
;
Diagnosis
;
Dysplastic Nevus Syndrome
;
Epidermis
;
Female
;
Humans
;
Melanins
9.Apocrine Mixed Tumor with Follicular Differentiation.
Hyun Jeong LEE ; Kee Young ROH ; Won Keun AHN ; Seog Jun HA ; Jin Wou KIM
Annals of Dermatology 2000;12(1):52-55
Mixed tumor of the skin (chondroid syringoma) is a rare benign tumor composed of epithelial elements intermingled with myxoid or cartilagenous stroma which is not separated by basement membrane. It had been believed to originate from the eccrine gland but recently, it was described to be of apocrine gland origin in case of showing apparent apocrine secretion. We report on a 63-year-old man with a tumor on the right upper eyelid showing typical microscopic features of mixed tumor of the skin. Many apocrine decapitation secretions were seen in tubular structures and follicular differentiations were also seen, which represents the common origin of folliculo-sebaceous-apocrine unit.
Adenoma, Pleomorphic
;
Apocrine Glands
;
Basement Membrane
;
Decapitation
;
Eccrine Glands
;
Eyelids
;
Humans
;
Middle Aged
;
Skin
10.Acquired Generalized Blue Nevi.
Hyun Jeong LEE ; Jong Gap PARK ; Seog Jun HA ; Won Keun AHN ; Jin Wou KIM
Annals of Dermatology 2000;12(1):41-43
Blue nevus is a benign melanocytic neoplasm and represents itself usually as a solitary blue or blue-black papule. It rarely occurs as multiple lesions grouped in a circumscribed area. How-ever, non-grouped disseminated blue nevi are exceedingly rare. We report a patient with acquired multiple blue nevi that was distributed over the entire body discretely and showed an increase in the number of the nevi without any causal factors.
Humans
;
Nevus
;
Nevus, Blue*