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Hypomelanosis of Ito with Multiple Congenital Anomalies

Yu DA, Kwon O, Kim KH

Hypomelanosis of Ito (HI) is a neurocutaneous disorder, also known as incontinentia pigmenti achromians. HI has been associated with chromosomal abnormalities, especially mosaicism. Herein, we report a case of HI...
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Depigmentation in a Patient with Chronic Myeloid Leukemia during Chemotherapy with Dasatinib

Choi YW, Na N, Park J

  • KMID: 2451599
  • Korean J Dermatol.
  • 2019 Jun;57(5):292-293.
No abstract available.
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Thorax masculinization in a transsexual patient: Inferior pedicle mastectomy without an inverted T scar

Cely AM, Triana CE, Triana LM

Transsexual individuals with gender dysphoria or gender identity disorder are rare, with a prevalence reported to range from 0.002% to 0.014%. Studies have shown that mastectomy yields significant improvements in...
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Analysis of Clinical Features and Treatment Outcomes Using 1,064-nm Nd-YAG Laser with Topical Hydroquinone in Patients with Riehl's Melanosis: A Retrospective Study in 10 Patients

Choi CW, Jo G, Lee DH, Jo SJ, Lee C, Mun JH

BACKGROUND: Hyperpigmentation on the face and neck can be a devastating psychological burden in patients with Riehl's melanosis. However, successful treatment of the disease is challenging for clinicians. OBJECTIVE: To evaluate...
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Atypical Pattern of Choroidal Hypopigmentation with Cutaneous Vitiligo

Kim M, Kwon JW, Park YH

No abstract available.
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Proper use of topical corticosteroids

Lee JH, Park YM

Topical corticosteroids are widely prescribed and used. As interest in the use of corticosteroids grows, people are increasingly exposed to misinformation that causes an excessive fear of side effects. Topical...
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Artemisia capillaris Thunb. inhibits melanin synthesis activity via ERK-dependent MITF pathway in B16/F10 melanoma cells

Saba E, Oh MJ, Lee YY, Kwak D, Kim S, Rhee MH

Genus Artemisia occurs as a hardy plant and has a wide range of culinary and medicinal features. In this study, we aimed to describe the melanin inhibitory activity of one...
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A Case of a Visual Field Defect with Optical Coherence Tomography Changes after Sildenafil Citrate Overdose

Park HS, Yang JY, Lee J

PURPOSE: A case of a transient visual field defect and a change in spectral-domain optical coherence tomography (SD-OCT) after an overdose of sildenafil citrate is described. CASE SUMMARY: A 67-year-old male...
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A Case of Punctate Leukoderma after 1,064 nm Q-Switched Nd:YAG Laser

Kwon O, Choi Y, Chung H, Park J

Punctate leukoderma is characterized of the destruction of melanocytes after chemical of physical damage. In addition, the term is broadly used to describe hypopigmented lesions induced in vitiligo patients after...
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The first Korean case of Waardenburg-Shah syndrome with novel endothelin receptor type B mutations

Lee ES, Ko JM, Moon JS

Waardenburg syndrome (WS) is a rare genetic disorder, including clinical features of pigmentary abnormalities of irides, skin, hair and sensorineural hearing loss and facial dysmorphism. Among the four types, WS...
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Treatment of Laser Therapy-Induced Punctate Leukoderma Using a 308-nm Excimer Laser

Jung HM, Kim H, Lee JH, Kim GM, Bae JM

Punctate leukoderma presents as numerous, distinct, round or oval depigmented spots. Recently, laser therapy-induced punctate leukoderma associated with various Q-switched laser and carbon dioxide laser have been reported. A 25-year-old...
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Telangiectasia Occurred after Neonatal Lupus Erythematosus

Park MY, Shim WH, Kim JM, Kim GW, Kim HS, Kim BS, Kim MB, Ko HC

  • KMID: 2386241
  • Korean J Dermatol.
  • 2017 Jun;55(5):297-300.
Neonatal lupus erythematosus (NLE) is an uncommon autoimmune disease that is associated with transplacental passage of maternal autoantibodies into the fetal circulation. It is commonly presented as multiple round, pink...
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Successful Repigmentation of Vitiligo-Like Hypopigmentation in a Case of Acanthosis Nigricans

Chun SH, Park JH, Park JB, Kim IH

No abstract available.
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Dermoscopic Features of Small, Medium, and Large-Sized Congenital Melanocytic Nevi

Cengiz FP, Emiroglu N, Ozkaya DB, Su O, Onsun N

BACKGROUND: Congenital melanocytic nevi (CMN) are present at birth. It is well known that the presence of large-sized congenital nevus in early life could predict a major risk of developing...
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A Case of Serious Complication after Cryotherapy

Kim JH, Oh S, Jun JY, Shim JH, Park JH, Lee JH, Lee DY, Lee JH, Yang JM

  • KMID: 2162223
  • Korean J Dermatol.
  • 2016 Mar;54(3):203-205.
Cryotherapy is a simple, relatively inexpensive therapeutic modality that is widely-used in clinical practice. It is especially appropriate for patients with an intolerance to anesthesia as well as high risk...
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Hypopigmentation Induced by Frequent Low-Fluence, Large-Spot-Size QS Nd:YAG Laser Treatments

Wong Y, Lee SS, Goh CL

The Q-switched 1064-nm neodymium-doped yttrium aluminum garnet (QS 1064-nm Nd:YAG) laser is increasingly used for nonablative skin rejuvenation or "laser toning" for melasma. Multiple and frequent low-fluence, large-spot-size treatments are...
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Changes in Melanin and Melanocytes in Mottled Hypopigmentation after Low-Fluence 1,064-nm Q-Switched Nd:YAG Laser Treatment for Melasma

Jang YH, Park JY, Park YJ, Kang HY

No abstract available.
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Clinicopathologic Features of Progressive Macular Hypomelanosis in Korea

Lee HS, Sohn S, Kang HY, Lee ES, Kim YC

  • KMID: 2246225
  • Korean J Dermatol.
  • 2015 Feb;53(2):113-118.
BACKGROUND: Progressive macular hypomelanosis, a disease of uncertain etiology, was first described by Guillet et al. in 1988. It is characterized by asymptomatic hypopigmented macules and patches that appear on...
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KHG26792 Inhibits Melanin Synthesis in Mel-Ab Cells and a Skin Equivalent Model

Li H, Kim J, Hahn HG, Yun J, Jeong HS, Yun HY, Baek KJ, Kwon NS, Min YS, Park KC, Kim DS

The purpose of this study is to characterize the effects of KHG26792 (3-(naphthalen-2-yl(propoxy) methyl)azetidine hydrochloride), a potential skin whitening agent, on melanin synthesis and identify the underlying mechanism of action....
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Griscelli syndrome type 2: a novel mutation in RAB27A gene with different clinical features in 2 siblings: a diagnostic conundrum

Mishra K, Singla S, Sharma S, Saxena R, Batra VV

Griscelli syndrome type 2 (GS2) is a rare autosomal recessive disease caused by mutations in the RAB27A gene. It is characterized by cutaneous hypopigmentation, immunodeficiency, and hemophagocytic lymphohistiocytosis. We describe...
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