1.A Case of Multiple and Extensive Becker's Nevus.
Gwang Yeol JOH ; Ai Young LEE ; Jai Il YOUN ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(6):664-667
Becker's nevus or Becker's melanosis is a distinct clinical entity in which epimal thickening may be minimal and hairiness and pigmentation obvious. 1Ne report a case of 14-year-old female suffering from Beckers melanosis with multiple and extensive skin lesions. The electron microscope revealed that the melanocytes were bulky with increased melanogenesis and an increased number of melanosomes was found in the keratinocytes. In addition, a large number of melanosomes were seen individually in the keratinocytes.
Adolescent
;
Female
;
Humans
;
Keratinocytes
;
Melanocytes
;
Melanosis
;
Melanosomes
;
Nevus*
;
Pigmentation
;
Skin
2.Eczema Confined to Becker's Nevus on the Face: The Behavior of Melanocytes during Inflammation.
Annals of Dermatology 2012;24(1):99-100
No abstract available.
Eczema
;
Inflammation
;
Melanocytes
;
Nevus
3.Effect of All-trans-retinoic Acid on the Growth and cAMP Level in Cultured Normal Human Melanocytes Stimulated by a-MSH.
Korean Journal of Dermatology 1999;37(8):1017-1028
No abstract available.
Humans*
;
Melanocytes*
;
Tretinoin*
4.Early Involvement of Hair Melanocytes Prior to Epidermal Melanocytes in the Progress of Halo Nevus.
Korean Journal of Dermatology 2016;54(2):151-153
No abstract available.
Hair*
;
Melanocytes*
;
Nevus, Halo*
5.Five Cases of Agminated Lentigines.
Seung Hyun HONG ; Jin Ho HONG ; Hae Jun SONG ; Chil Hwan OH
Korean Journal of Dermatology 1995;33(5):983-987
Agminated lentigines may be defind as a circumscribed grouping of small pigmented macules arranged in a small or large group, often in a segmental pattern, each macule consisting of a lentiginous epidermal proliferation of melanocytes. We report five cases of agminated lentigines in otherwise healthy persons. Histologic exarnination of the pigmented lesion revealed findings consistent with lentigo simplex.
Humans
;
Lentigo*
;
Melanocytes
6.Comparison of the human melanocyte culture in phorbol 12-myristate 13-acetate-contained medium and physiologic mitogens-contained medium.
Mu Hyoung LEE ; Ji Ho RYOU ; Bum Jin JUBH
Korean Journal of Dermatology 1999;37(2):168-176
BACKGROUND: The growth of cells is closely related to components in a culture medium. There are many reports about cellular characteristics of melanocytes grown in a PMA-contained medium. However, only a few reports have been studied by using a physiologic mitogens-contained medium. To understand melanocyte in vivo, it is necessary to know the cellular biology of melanocytes grown in a physiologic mitogens-contained medium. OBJECTIVE: To investigate any differences between melanocytes grown in phorbol 12-myristate 13-acetate(PMA)-contained medium and in physiologic mitogens-contained medium. METHOD: We examined morphology, number and melanin contents of cultured human melanocytes grown in a PMA-contained medium and physiologic mitogens-, such as bFGF, ET-1 and a a-MSH contained medium. Result : The results are summarized as follows : 1. There were no significant morphologic differences between cells in PMA-contained medium and in physiologic mitogens-contained medium. 2. The number of melanocytes were significantly more numerous in PMA-contained medium on the 2nd day (p<0.05), but significantly less numerous in the same medium on the 6th day (p<0.05). So, the proliferation rate of melanocytes in PMA-contained medium became lower than in physiologic mitogens-contained medium as time went by. 3. Melanocytes grown in PMA-contained medium had significantly increased melanin contents regardless of the time (p<0.05). Conclusion : The proliferation of melanocytes was better in physiologic mitogens-contained medium, the melanization was higher in melanocytes of PMA-contained medium.
Humans*
;
Melanins
;
Melanocytes*
7.Changes in Melanin and Melanocytes in Mottled Hypopigmentation after Low-Fluence 1,064-nm Q-Switched Nd:YAG Laser Treatment for Melasma.
Yong Hyun JANG ; Ji Youn PARK ; Young Joon PARK ; Hee Young KANG
Annals of Dermatology 2015;27(3):340-342
No abstract available.
Hypopigmentation*
;
Melanins*
;
Melanocytes*
;
Melanosis*
8.A Simple Assay Method for Melanosome Transfer.
Hye Ryung CHOI ; So Hee PARK ; Jae Woo CHOI ; Dong Seok KIM ; Kyung Chan PARK
Annals of Dermatology 2012;24(1):90-93
Pigmentation is induced by production of melanin in specialized organelles termed melanosomes and by transfer of these organelles from melanocytes to surrounding keratinocytes. The chemical basis of melanogenesis is relatively well known but the mechanism of melanosome transfer is not well studied. Various pigmentary disorders and cosmetic applications require the use of depigmenting agents. Currently available topical agents used for the reduction of pigmentation mainly include tyrosinase inhibitors and/or melanocyte-cytotoxic agents. Recently, several agents have been introduced to inhibit melanosome transfer from melanocytes to keratinocytes. However, an experimental model for melanosome transfer is not well established. In this study, a simple assay method using flow cytometry is described.
Cosmetics
;
Flow Cytometry
;
Keratinocytes
;
Melanins
;
Melanocytes
;
Melanosomes
;
Models, Theoretical
;
Monophenol Monooxygenase
;
Organelles
;
Pigmentation
9.The effect of topical melatonin on epidermal melanocytes in uv-irradiated black mice.
Sung Ha LEE ; Jong Woo LEE ; Jin Sik BURM ; Chul Hoon CHUNG ; Suk Joon OH
Journal of the Korean Society of Plastic and Reconstructive Surgeons 1998;25(3):346-354
Melatonin was derived from pineal gland, act as hormone and is known to be extremely active in certain biological systems. To observe the depigmentation effet of melatonin, author induced activation of melanocytes and melanin by UVB irradiation for seven days and then melatonin ointment or ointment base was applied topically on the ear skin of C57 B1 mouse. Tissue samples were obtained from 4 mice in each group before and after UVB irradiation for given days(1,3,5 and 7 week). The morphological, numerical, and ultrastructural changes of epidermal melanocytes were observed with light microscope and electron miroscope after DOPA stain. The results were as follows: 1) In all groups, the number of DOPA positive melanocytes began to decrease from 1 week. 2) The number of DOPA-positive melanocytes in melatonin ointment applied group was significantly lower than in control group. 3) In the electron microscopic findings, the number of melanosomes markedly decreased from 1 week to 7 weeks and a small amount of destructed melanosomes(vacuoles) and destroyed or swollen mitochondria in cytoplasm of th melanocyte appeared more significant in 3% melatonin ointment applied group compared to ointment base applied group from 5 weeks.
Animals
;
Cytoplasm
;
Dihydroxyphenylalanine
;
Ear
;
Melanins
;
Melanocytes*
;
Melanosomes
;
Melatonin*
;
Mice*
;
Mitochondria
;
Pineal Gland
;
Skin
10.Effect of Sulfhydryl Compounds on Melanosomal Morphology of Epidermal Melanocytes in UV - Irradiated Black Mice.
Kyung Won HAN ; Ki Bum MYUNG ; Jeong Hee HAHM ; Hong Il KOOK
Korean Journal of Dermatology 1987;25(5):553-561
The present study was performed to evaluate the effect of sulfhydryl compounds, cysteine and glutathione, on the size of melanosomes and the ratio of melanosormai stages of epidermal melanocytes in UV-irradiated black mice. The results were as follows; 1. Both of cysteine and glutathione showed significant diminution in the short axis of melanosomes and the percentage of stage 4 melanosomes of epidermal melanocytes in C57BL black mice skin. 2. The length of short axis of melanosomes in glutathione-treated group is smaller than those in cysteine-treated group at the end of 3rd week of intraperitoneal injection. The percentage of stage IV melanosomes significantly decreased in glutathione-treated group and cysteine-treated group at the end of 3rd week and 5th week respectively. 3. In glutathione-treated group, the short axis of melanosomes and the percentage of stage 4 melanosomes both decreased in proportional to the period of intraperitoneal in]ection.
Animals
;
Axis, Cervical Vertebra
;
Cysteine
;
Glutathione
;
Injections, Intraperitoneal
;
Melanocytes*
;
Melanosomes
;
Mice*
;
Skin
;
Sulfhydryl Compounds*