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1.
Annals of Dermatology ; : 192-201, 2018.
Artigo em Inglês | WPRIM | ID: wpr-714159

RESUMO

BACKGROUND: Folliculotropic mycosis fungoides (FMF) is a variant of mycosis fungoides (MF) that is characterized clinically by variable types of skin eruptions, including plaques, acneiform lesions, and alopecic patches. Histopathologically, FMF is characterized by folliculotropic infiltrates. OBJECTIVE: This study was conducted to scrutinize the clinical and histopathologic features of FMF in Koreans and the responses to phototherapy. METHODS: Twenty Koreans diagnosed with MF who had histopathologic evidence of folliculotropism were enrolled. RESULTS: Eighteen patients had head-and-neck-region infiltration, while five had solitary lesion. In all patients, the atypical lymphocytic infiltrate had a perifollicular distribution. Twelve patients were treated with ultraviolet A (UVA)-1. Eleven of these 12 patients with early-stage FMF experienced >80% improvement (8: complete remission; 3: partial remission). Four patients, including 2 who relapsed after UVA-1, were treated with photodynamic therapy (PDT), reaching complete remission after PDT. CONCLUSION: As FMF has variable clinical presentations, skin biopsy is required to confirm the diagnosis. And both UVA-1 and methyl aminolevulinate-PDT are clinically effective in treatment of early-stage FMF.


Assuntos
Humanos , Biópsia , Diagnóstico , Micose Fungoide , Fotoquimioterapia , Fototerapia , Pele
2.
Korean Journal of Dermatology ; : 499-503, 2018.
Artigo em Coreano | WPRIM | ID: wpr-717026

RESUMO

Wells' syndrome or eosinophilic cellulitis is usually observed in adults who present with pruritic, erythematous and edematous plaques associated with papules or vesicles. It is a rare inflammatory dermatosis of unknown etiology showing an eosinophil-mediated immune response. Classical histopathological features observed in patients are eosinophil-predominant inflammatory infiltration and marked dermal edema, along with ‘flame figures’. An 11-year-old boy presented with edematous plaques surmounted by vesicles on his abdomen and lower extremities. A month prior to presentation, these skin lesions occurred on other parts of his abdomen; however, they resolved spontaneously within a week. Skin biopsies from the recurrent lesions showed features consistent with Wells' syndrome and a few molluscum bodies in the epidermis. Laboratory tests showed peripheral eosinophilia. We concluded that Wells' syndrome in this young patient was caused by preceding molluscum contagiosum infection.


Assuntos
Adulto , Criança , Humanos , Masculino , Abdome , Biópsia , Celulite (Flegmão) , Edema , Eosinofilia , Eosinófilos , Epiderme , Extremidade Inferior , Molusco Contagioso , Pele , Dermatopatias
3.
Annals of Dermatology ; : 510-510, 2018.
Artigo em Inglês | WPRIM | ID: wpr-716480

RESUMO

In the originally published version of this article, complete anonymity was not achieved.

4.
Annals of Dermatology ; : 471-475, 2017.
Artigo em Inglês | WPRIM | ID: wpr-86512

RESUMO

Nocardia species are aerobic, gram-positive, filamentous, partially acid-fast actinomycetes which are found worldwide in soil and decaying organic plant matter. When they infect human beings, they generally enter through the respiratory tract and then disseminate systemically. Rarely has a primary infection occurred as the result of direct inoculation. Isolation of Nocardia from clinical specimens and identification of species are difficult. But, with the introduction of new genetic technologies, reports of novel species of Nocardia have increased. We describe a case of cutaneous nocardiosis caused by Nocardia takedensis in an 87-year-old woman who was diagnosed by bacterial culture and 16S ribosomal RNA sequencing. N. takedensis has been described as a new species. This report describes the first clinical isolate of N. takedensis from a skin specimen in Korea.


Assuntos
Idoso de 80 Anos ou mais , Feminino , Humanos , Actinobacteria , Coreia (Geográfico) , Nocardiose , Nocardia , Plantas , Sistema Respiratório , RNA Ribossômico 16S , Pele , Solo
5.
Korean Journal of Dermatology ; : 614-621, 2016.
Artigo em Coreano | WPRIM | ID: wpr-183272

RESUMO

BACKGROUND: Although several traditional treatments have been applied for recalcitrant viral warts, these treatments have rarely resulted in complete recovery. To treat the recalcitrant viral wart, alternative therapies are required. OBJECTIVE: This study aimed to evaluate the efficacy and safety of quadrivalent HPV vaccine for recalcitrant wart treatment. METHODS: From 2012 to 2014, 17 patients who provided informed consent were enrolled. All patients received 3 doses of quadrivalent HPV vaccine at 0, 2, and 6 months, respectively. During clinic visits, doctors checked the grade of improvement, patient satisfaction, and treatment side effects. After completion of the 3 doses, the patients were followed up for 5 months with outpatient visits and telephone inquiries. RESULTS: After the third dose, 58.8% of patients showed complete remission and 41.2% showed no response after 5 months. There were no statistically significant differences in sex, age, disease duration, number, anatomic site, and previous treatment between the complete remission group and the no-response group. An adverse effect (syncope) was observed in one patient. CONCLUSION: Compared with traditional aggressive therapies, quadrivalent HPV vaccine is a simple method and does not usually interfere with the patient's work or social life. Quadrivalent HPV vaccine is an effective and safe alternative treatment for recalcitrant warts.


Assuntos
Humanos , Assistência Ambulatorial , Estudo Clínico , Terapias Complementares , Consentimento Livre e Esclarecido , Métodos , Pacientes Ambulatoriais , Papillomaviridae , Satisfação do Paciente , Telefone , Verrugas
6.
Korean Journal of Dermatology ; : 814-818, 2016.
Artigo em Coreano | WPRIM | ID: wpr-18916

RESUMO

Self-healing juvenile cutaneous mucinosis (SHJCM) is a rare disorder of unknown origin that affects healthy children. It is characterized by multiplication of transient papules and nodules on the head and periarticular area. Histopathologically, lesions show mucin deposition in the dermis or subcutis. A 9-year-old male patient presented with multiple skin-colored papules and nodules on the face and both hands. These papules and nodules had appeared over the preceding months and had been increasing in number. He was otherwise healthy and had no underlying systemic disorders. Skin biopsy in the right thenar nodule revealed deposition of amorphous material stained positively with Alcian blue (pH 2.5) within the dermis and subcutis. Spontaneous resolution occurred over several months without sequelae.


Assuntos
Criança , Humanos , Masculino , Azul Alciano , Biópsia , Derme , Mãos , Cabeça , Mucinoses , Mucinas , Pele
7.
Korean Journal of Dermatology ; : 556-559, 2015.
Artigo em Coreano | WPRIM | ID: wpr-92764

RESUMO

Squamous cell carcinoma commonly originates from recalcitrant wound sites, including burn scars, pressure sores, stasis ulcers, osteomyelitis, and sites of frostbite. A 62-year-old male was referred to the dermatology department for skin necrosis of his right great toe and walking difficulty. He had a history of smoking, drinking alcohol, and frostbite of his right great toe 9 years prior, which deteriorated into osteomyelitis due to poor care. Although a skin biopsy was recommended before amputation, the two procedures were performed simultaneously due to a lack of toe function due to severe osteolysis. Biopsy of the amputated toe tip showed many lobules consisting of atypical keratinocytes with hyperchromatic nuclei, and severe dermal pleomorphism. After evaluation for distant metastasis, including a (99m) Tc-MDP bone scan, 18F-FDG positron emission tomography scan, computed tomography, and ultrasound, no metastasis was detected.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Amputação Cirúrgica , Biópsia , Queimaduras , Carcinoma de Células Escamosas , Cicatriz , Dermatologia , Ingestão de Líquidos , Fluordesoxiglucose F18 , Congelamento das Extremidades , Queratinócitos , Necrose , Metástase Neoplásica , Osteólise , Osteomielite , Tomografia por Emissão de Pósitrons , Úlcera por Pressão , Pele , Fumaça , Fumar , Dedos do Pé , Ultrassonografia , Úlcera Varicosa , Caminhada , Ferimentos e Lesões
8.
Annals of Dermatology ; : 759-762, 2015.
Artigo em Inglês | WPRIM | ID: wpr-164326

RESUMO

Cutaneous and systemic plasmacytosis (CSP) is a rare disorder of unknown etiology characterized by cutaneous polyclonal plasma cell infiltrates associated with various extracutaneous involvement and polyclonal hypergammaglobulinemia. Here, we report on a 54-year-old male patient with chronic renal insufficiency who presented with disseminated reddish-brown macules and plaques on the face and trunk. In our evaluation, he was found to have lymphadenopathy, polyclonal hypergammaglobulinemia; benign plasma cell infiltration involving the skin, bone marrow, and retroperitoneal area; and renal amyloidosis. To the best of our knowledge, this is the first reported case of CSP associated with renal amyloidosis.


Assuntos
Humanos , Masculino , Pessoa de Meia-Idade , Amiloidose , Medula Óssea , Hipergamaglobulinemia , Doenças Linfáticas , Plasmócitos , Insuficiência Renal Crônica , Pele
9.
Korean Journal of Dermatology ; : 199-200, 2014.
Artigo em Coreano | WPRIM | ID: wpr-192875

RESUMO

No abstract available.


Assuntos
Cisto Epidérmico
10.
Korean Journal of Dermatology ; : 442-443, 2014.
Artigo em Coreano | WPRIM | ID: wpr-156834

RESUMO

No abstract available.


Assuntos
Humanos , Papiloma , Verrugas
11.
Korean Journal of Dermatology ; : 654-657, 2014.
Artigo em Coreano | WPRIM | ID: wpr-170788

RESUMO

Eccrine syringofibroadenoma (ESFA) is a rare, benign adnexal neoplasm of eccrine differentiation. It is typically located on the limbs and presents as a plaque or a solitary hyperkeratotic nodule in an adult. However, there are several clinical subtypes, ranging from a solitary papule or nodule to multiple lesions with linear or diffuse distribution. Despite the diverse clinical presentation, ESFA is histologically similar. It commonly shows proliferation of anastomosing cords and strands of cuboidal epithelial cells with or without lumina embedded in a fibrovascular stroma. Herein, we report an unusual case of ESFA with verrucous surfaced plaque present on the scalp since birth in a 22-year-old man.


Assuntos
Adulto , Humanos , Adulto Jovem , Células Epiteliais , Extremidades , Nevo , Parto , Couro Cabeludo
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