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1.
Korean Journal of Dermatology ; : 48-49, 2019.
Artigo em Inglês | WPRIM | ID: wpr-719698

RESUMO

No abstract available.


Assuntos
Leiomioma , Escroto
6.
Korean Journal of Dermatology ; : 194-196, 2019.
Artigo em Coreano | WPRIM | ID: wpr-759712

RESUMO

Dermatofibroma is a fibrohistiocytic tumor of the skin that commonly occurs as a solitary lesion on the lower extremities of young women. Multiple eruptive dermatofibromas (MEDFs), defined as the presence of 5 to 8 dermatofibromas appearing within a period of 4 months, are rare, and the etiology of MEDFs remains unknown. However, MEDFs are frequently thought to be associated with altered immunity, such as autoimmune diseases and immunosuppression. It is unclear why MEDFs occur in association with these conditions, but this relationship may suggest that MEDFs are the result of an abortive immunoreactive process. We herein describe a middle-aged woman who developed multiple dermatofibroma. She had myasthenia gravis for 8 years, and developed MEDFs after undergoing oral corticosteroid treatment (245 mg/week) for 3 months. Therefore, our case suggests that the use of immunosuppressants is a more dominant factor for the development of MEDFs than underlying autoimmune diseases.


Assuntos
Feminino , Humanos , Doenças Autoimunes , Histiocitoma Fibroso Benigno , Terapia de Imunossupressão , Imunossupressores , Extremidade Inferior , Miastenia Gravis , Pele
7.
Annals of Dermatology ; : 729-730, 2018.
Artigo em Inglês | WPRIM | ID: wpr-718544

RESUMO

No abstract available.


Assuntos
Doença de Darier , Pitiríase
8.
Korean Journal of Dermatology ; : 494-498, 2018.
Artigo em Coreano | WPRIM | ID: wpr-717027

RESUMO

Trichorhinophalangeal syndrome (TRPS) is a rare autosomal dominant hereditary disease caused by mutations in the TRPS1 or the EXT1 gene. Patients show 3 different forms (TRPS I-TRPS III) of this condition sharing similar clinical features including sparse hair, a bulbous nose, an elongated philtrum, short stature, and shortened phalanges. A 10-year-old girl presented with sparse hair and thin hair shafts since birth. She also showed a bulbous nose, an elongated philtrum, brachydactyly of the great toes, and a short stature. Radiological examination showed cone-shaped epiphyses and shortened phalanges. Genetic analysis revealed a novel missense mutation c.2759G>C (p.Trp920Ser) in the TRPS1 gene. We diagnosed this patient with TRPS type III. To our knowledge, only 3 reports have described a genetically analyzed TRPS1 gene mutation among the 11 reported cases of TRPS in the Korean literature. Furthermore, we identified a novel missense mutation in the TRPS1 gene.


Assuntos
Criança , Feminino , Humanos , Braquidactilia , Epífises , Doenças Genéticas Inatas , Cabelo , Lábio , Mutação de Sentido Incorreto , Nariz , Parto , Dedos do Pé
9.
Annals of Dermatology ; : 508-509, 2018.
Artigo em Inglês | WPRIM | ID: wpr-716481

RESUMO

No abstract available.


Assuntos
Hipertricose , Neurilemoma
10.
Korean Journal of Dermatology ; : 202-205, 2018.
Artigo em Coreano | WPRIM | ID: wpr-713427

RESUMO

Rudimentary polydactyly is a congenital anomaly of the hand clinically ranging from a small wart-like tumor to a pedunculated structure near the thumb or little finger. The histology reveals a marked neural proliferation, dilated blood vessels, and some Meissner corpuscles in the dermis. The etiology is unknown and there are a few theories. First, Hare believed that it represented a vestigial form of supernumerary finger, and termed it rudimentary polydactyly. Since then, Shapiro et al. has argued that rudimentary polydactyly is an amputation neuroma after finding histological similarity between acquired traumatic neuroma and rudimentary polydactyly. Recently Brehmer- Andersson et al. asserted that rudimentary polydactyly is a neuroma that can arise in any area containing Meissner corpuscles after observing a penile lesion with similar histology as rudimentary polydactyly. We report a case of rudimentary polydactyly characteristically not showing any prominent Meissner corpuscles. With this case, we provide support for the theory of Shapiro et al.


Assuntos
Amputação Cirúrgica , Vasos Sanguíneos , Derme , Dedos , Mãos , Lebres , Neuroma , Polidactilia , Polegar
13.
Annals of Dermatology ; : 331-334, 2018.
Artigo em Inglês | WPRIM | ID: wpr-715491

RESUMO

BACKGROUND: Labial melanotic macules (LMMs) are benign pigmented lesions that usually take the shape of flat asymmetrical macules with tan-brown to black color and variable size. Whereas the dermoscopic features of other pigmented skin lesions have been relatively well described, little is known about LMMs. OBJECTIVE: To describe the dermoscopic features and find typical and schematic dermoscopic patterns in LMMs. METHODS: A retrospective dermoscopic study was conducted on 80 lesions with histopathologically proved LMMs. RESULTS: We described and defined, for the first time to our knowledge, landscape painting patterns found in 65 of 80 melanotic lesions (81.3%), characterized by parallel lines or circle lines, overlapping vessels with background brown pigmentation. The background brown pigmentations were observed in 74 of 80 lesions (92.5%), the parallel lines in 62 (77.5%), the circle lines in 20 (25.0%), and overlapping vessels in 69 (86.3%). The structureless black pigmentations were only presented in 26 of 80 (32.5%). CONCLUSION: Dermoscopy can be useful for the clinical detection of LMMs, and “Landscape painting patterns” may represent a dermoscopic clue for the diagnosis of these lesions.


Assuntos
Dermoscopia , Diagnóstico , Pintura , Pinturas , Pigmentação , Estudos Retrospectivos , Pele
16.
Korean Journal of Dermatology ; : 273-275, 2018.
Artigo em Coreano | WPRIM | ID: wpr-714496

RESUMO

Unilateral linear capillaritis (ULC) is a rare variant of pigmented purpuric dermatosis (PPD). ULC is clinically characterized by unilateral linear macules on the lower extremities, which fade spontaneously. We present three patients with linearly distributed purpuric macules on only one side of the lower extremities. Skin biopsy showed histopathological features of PPDs. We diagnosed ULC based on these clinicopathological findings. For all patients, the skin lesions began to fade spontaneously within several months to a few years after onset. ULC has been reported rarely, with only about 20 cases worldwide and no cases described in the Korean literature.


Assuntos
Humanos , Biópsia , Extremidade Inferior , Pele , Dermatopatias
18.
Annals of Dermatology ; : 86-90, 2017.
Artigo em Inglês | WPRIM | ID: wpr-132704

RESUMO

Phytophotodermatitis is a condition caused by sequential exposure to photosensitizing substances present in plants followed by ultraviolet light. Several plants (e.g., limes, celery, fig, and wild parsnip) contain furocoumarin compounds (psoralens). It is important for dermatologists to be aware of phytophotodermatitis because it may be misdiagnosed as cellulitis, tinea, or allergic contact dermatitis. We present five patients with a sharply defined erythematous swollen patch with bullae on both feet. They described soaking their feet in a fig leaves decoction to treat their underlying dermatologic diseases. Within 24 hours, all patients had a burning sensation in their feet, and erythema and edema had developed on the feet dorsa with exception of the portion of the skin covered by the sandals. Histopathologic examinations revealed sub-epithelial blisters with intensive epidermal necrosis. Phytophotodermatitis was ultimately diagnosed and, after several days, the patients' skin lesions began to recover upon treatment with systemic and topical corticosteroids. Unfortunately, since there are no studies providing sufficient evidence on the benefits of fig leaves, they should be used with caution.


Assuntos
Humanos , Corticosteroides , Apium , Vesícula , Queimaduras , Celulite (Flegmão) , Citrus aurantiifolia , Dermatite Alérgica de Contato , Edema , Eritema , Ficus , , Necrose , Transtornos de Fotossensibilidade , Sensação , Pele , Tinha , Raios Ultravioleta
19.
Annals of Dermatology ; : 86-90, 2017.
Artigo em Inglês | WPRIM | ID: wpr-132701

RESUMO

Phytophotodermatitis is a condition caused by sequential exposure to photosensitizing substances present in plants followed by ultraviolet light. Several plants (e.g., limes, celery, fig, and wild parsnip) contain furocoumarin compounds (psoralens). It is important for dermatologists to be aware of phytophotodermatitis because it may be misdiagnosed as cellulitis, tinea, or allergic contact dermatitis. We present five patients with a sharply defined erythematous swollen patch with bullae on both feet. They described soaking their feet in a fig leaves decoction to treat their underlying dermatologic diseases. Within 24 hours, all patients had a burning sensation in their feet, and erythema and edema had developed on the feet dorsa with exception of the portion of the skin covered by the sandals. Histopathologic examinations revealed sub-epithelial blisters with intensive epidermal necrosis. Phytophotodermatitis was ultimately diagnosed and, after several days, the patients' skin lesions began to recover upon treatment with systemic and topical corticosteroids. Unfortunately, since there are no studies providing sufficient evidence on the benefits of fig leaves, they should be used with caution.


Assuntos
Humanos , Corticosteroides , Apium , Vesícula , Queimaduras , Celulite (Flegmão) , Citrus aurantiifolia , Dermatite Alérgica de Contato , Edema , Eritema , Ficus , , Necrose , Transtornos de Fotossensibilidade , Sensação , Pele , Tinha , Raios Ultravioleta
20.
Annals of Dermatology ; : 433-437, 2017.
Artigo em Inglês | WPRIM | ID: wpr-86517

RESUMO

BACKGROUND: The incidence and mortality rates associated with cutaneous melanoma (CM) have steadily increased over the last 20 years. Even with successful treatment, melanoma patients usually experience substantial anxiety regarding the development of terrible recurrence. To date, few studies have investigated various dermatoses what the patients with CM had anxiety for the recurrence during postoperative surveillance (Dw). OBJECTIVE: To describe various Dw and to evaluate the risk of subsequent malignant skin disease in patients with CM. METHODS: We performed a prospective study between August 2002 and August 2015. RESULTS: Fifty-six patients presented with a total of 68 Dw. Among them, melanocytic nevus was the most common (n=27), followed by seborrheic keratosis (n=9) and CM recurrence (n=7). Approximately 5.6% of the lesions were diagnosed as malignant skin diseases. This was a single-center study, so the prevalence of malignant skin diseases following primary melanoma may not represent that of all patients with CM. CONCLUSION: The results of this study can be referred by dermatologists dealing with melanoma especially when CM patients have too excessive or unrealistic anxiety for melanoma recurrence during postoperative surveillance of CM. However, the importance of postoperative surveillance must still be emphasized because of real risk of melanoma recurrence and other malignant skin.


Assuntos
Humanos , Ansiedade , Incidência , Ceratose Seborreica , Melanoma , Mortalidade , Nevo Pigmentado , Prevalência , Estudos Prospectivos , Recidiva , Pele , Dermatopatias
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