1.Generalized Schamberg Disease in a Child.
Annals of Dermatology 2013;25(4):524-525
No abstract available.
Child*
;
Humans
;
Pigmentation Disorders*
2.Hypomelanosis of Ito
Pandare SUGATHAN ; André GRABOWSKI
Brunei International Medical Journal 2012;8(3):139-144
Hypomelanosis of Ito (HI) is a rare neurocutaneous syndrome with characteristic whirled hypopigmented skin lesions and neurological manifestations. Less consistently, there may be non-neurological manifestations that include ophthalmic, musculoskeletal, craniofacial, cardiac, genitourinary, and gastrointestinal involvements. We report a case of HI, with typical skin lesions in association with hemimegalencephaly, seizures and mental retardation along with the hitherto unreported repetitive hand movements such as seen in Rett syndrome.
Hemimegalencephaly
;
Ito syndrome
;
Pigmentation disorders
3.Additional Comments on 'Clinical Trial to Evaluate the Efficacy and Safety of a Home-use Intense Pulsed Light Device for Hair Removal, Treatment of Acne and Pigmentation Disorders, and Fine Wrinkle Reduction'.
Seonguk MIN ; Hyuck Hoon KWON ; Seon Yong PARK ; Ji Young YOON ; Dae Hun SUH
Korean Journal of Dermatology 2015;53(1):88-88
No abstract available.
Acne Vulgaris*
;
Hair Removal*
;
Pigmentation Disorders*
4.A Case of Post-Herpetic Nevoid Comedones
Jong Kil SEO ; Ki Heon JEONG ; Min Kyung SHIN
Annals of Dermatology 2019;31(Suppl):S36-S38
No abstract available.
Skin Abnormalities
;
Herpesviridae Infections
;
Pigmentation Disorders
;
Hamartoma
5.A Case of Dyschromatosis Universalis Hereditaria Treated with a Q-switched Nd:YAG Laser.
Dae Hyun KIM ; Hyuk KWON ; Young Lip PARK ; Sanghoon LEE ; Kyu Uang WHANG ; Moon Kyun CHO ; Jong Suk LEE ; Sung Yul LEE
Korean Journal of Dermatology 2009;47(10):1166-1171
Dyschromatosis universalis hereditaria is a rare pigmentary disorder that's characterized by the presence of both small and irregular sized hyperpigmented and hypopigmented macules in a generalized distribution. The pattern of inheritance is thought to be autosomal dominant, but some sporadic and autosomal recessive inheritance cases have also been reported. We report here on a case of a-15-year old female patient with dyschromatosis universalis hereditaria, which is compatible with autosomal dominant inheritance. The patient presented with numerous small and irregularly sized hyper-and hypopigmented macules on her face, trunk and both the arms and legs, but not on the palms and soles. By analysis of her familial pedigree, we found an autosomal dominant pattern of inheritance. The biopsy specimen taken from the hyperpigmented macules showed increased melanin granules and pigmentation in the basal cell layer of the epidermis. Various therapeutic trials have been introduced to treat these lesions, but there have been few reports of simple effective treatments for the hyper-and hypopigmented lesions. So, we tried treating the hyperpigmented macules with a Q-switched Nd:YAG laser and we obtained a successful result.
Arm
;
Biopsy
;
Epidermis
;
Female
;
Humans
;
Hyperpigmentation
;
Leg
;
Melanins
;
Pedigree
;
Pigmentation
;
Pigmentation Disorders
;
Skin Diseases, Genetic
;
Wills
6.Clinical Trial to Evaluate the Efficacy and Safety of a Home-use Intense Pulsed Light Device for Hair Removal, Treatment of Acne and Pigmentation Disorders, and Fine Wrinkle Reduction.
Seonguk MIN ; Hyuck Hoon KWON ; Seon Yong PARK ; Ji Young YOON ; Dae Hun SUH
Korean Journal of Dermatology 2014;52(12):880-891
BACKGROUND: Home-use devices designed for cosmetic purposes have recently gained popularity. Small, low-energy, low-cost intense pulsed light (IPL) systems provide safe, convenient, and private treatment for several medical conditions. OBJECTIVE: In this study, we aimed to assess the efficacy and safety of a home-use IPL device for hair removal, acne treatment, achieving a whitening effect for hyperpigmentation, and wrinkle reduction. METHODS: Five IPL hair removal treatment sessions were performed at 1-week intervals. A total of 10 sessions were performed in a split-face manner for other medical conditions. Four independent randomized controlled trials were performed using a blind evaluation method. All subjects were followed up twice to evaluate the maintenance of efficacy. RESULTS: A significant reduction in hair was observed via trichoscopy following two sessions of treatment (p<0.001). A mean hair reduction of 80% was observed at week 4; however this returned to the previous state upon cessation of treatment. Acne grading decreased from 2.6 to 1.1 at week 8, and IPL treatment induced a significant reduction in melanin index after 2 weeks. The average values of the difference of R2 (Cutometer(R)) between IPL-treated areas and baseline were higher than those of the difference of R2 between control area and baseline. CONCLUSION: This home-use IPL device was effective for hair removal and treatment of acne, hyperpigmentation, and wrinkles.
Acne Vulgaris*
;
Hair
;
Hair Removal*
;
Hyperpigmentation
;
Melanins
;
Pigmentation
;
Pigmentation Disorders*
;
Withholding Treatment
7.Incontinentia Pigmenti Achromians ( Ito ): Report of two cases.
Korean Journal of Dermatology 1976;14(1):81-85
Incontinentia pigmenti acb.romians(Ito) is characterized by progressive bizarre or whorl-like hypopigmentation on trunk and extrementies during childhood. It is similar to a negative picture of incontinentia pigmenti(Blocb-Sulzberger) and not infrequently associated with mental, bony and ocular defects. The incidence of this disease is predominent in femaIe without hereditary background. Case 1. Two years old female was visited to our clinic because of mottled depigmented patches on right thigh for about 8 months. Case 2. 14 months oId female was visited to our clinic because of linear and. mottled depigmented natches on their limbs for about 7 months. Histopathological findings of both cases shows the focal depigmentation on basal layer. They are treated with steroid ointment with moderate to good effects.
Extremities
;
Female
;
Humans
;
Hypopigmentation
;
Incidence
;
Incontinentia Pigmenti*
;
Pigmentation Disorders*
;
Thigh
8.A Case of Reticulate Acropigmentation of Dohi Presented on the Trunk.
Korean Journal of Dermatology 2008;46(8):1108-1111
Reticulate acropigmentation of Dohi is a rare dyschromic disorder that has an autosomal dominant pattern of inheritance. It presents generally during infancy or early childhood as symmetrical pinpoint to pea-sized hyperpigmented and hypopigmented macules on the back of the hands and feet. The eruption slowly extends proximally and may rarely affect the sides of the neck and upper portion of the trunk. We report a case of reticulate acropigmentation of Dohi on the trunk of a patient with a family history of the disorder in four generations. To our knowledge, this is the first report in the Korean literature that describes skin lesions on the trunk in a patient with reticulate acropigmentation of Dohi.
Family Characteristics
;
Foot
;
Hand
;
Humans
;
Neck
;
Pigmentation Disorders
;
Skin
;
Wills
9.A child with progressive pigmented purpuric dermatosis.
Xia WANG ; Huan YE ; Ji-yan ZHENG
Chinese Journal of Pediatrics 2005;43(10):798-799
Adolescent
;
Humans
;
Male
;
Pigmentation Disorders
;
pathology
;
Skin
;
pathology
10.A quantitative evaluation of pigmented skin lesions using the L*a*b* color coordinates.
Soo Chan KIM ; Deok Won KIM ; Joon Pio HONG ; Dong Kyun RAH
Yonsei Medical Journal 2000;41(3):333-339
The evaluation of pigmentary skin lesions by clinical doctors has been based on subjective and qualitative judgements. Observations have mostly relied on visual inspection, making the effects of treatment difficult to evaluate with any precision. For this reason there is a real need for an objective method to evaluate prognosis after treatment. Recent scientific measurements such as reflectance spectrophotometry and reflectance colorimetry have provided accurate quantitative color information about skin lesions, but these techniques are costly and difficult to apply in the clinical field. The purpose of this study was to develop a simple and cost-effective way of evaluating treatment results. We have developed a software program using the L*a*b* color coordinate system to quantify the effect of treatment and have successfully demonstrated its clinical usefulness. Our method compares the relative color difference between normal skin and skin lesions before and after treatment, instead of measuring the absolute color of skin lesions. The accuracy of our quantitative color analysis was confirmed by the simulated images of hemangioma and ota nevus. Clinical efficacy was also confirmed through a blind test involving 3 clinicians who were asked to grade the treatment effects of 13 cases of hemangioma and 7 cases of ota nevus. These subjective clinical grades correlated well with the treatment results obtained using the proposed color analysis system (Correlation coefficient = 0.84).
Color*
;
Female
;
Hemangioma/therapy
;
Hemangioma/pathology
;
Human
;
Nevus of Ota/therapy
;
Nevus of Ota/pathology
;
Outcome Assessment (Health Care)/methods*
;
Pigmentation Disorders/therapy*
;
Pigmentation Disorders/pathology*
;
Skin Neoplasms/therapy
;
Skin Neoplasms/pathology
;
Skin Pigmentation*
;
Software*