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대한피부과학회> 대한피부과학회지> 수포형이 동반된 다발성 모기질종

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수포형이 동반된 다발성 모기질종

Multiple Pilomatricomas with a Bullous Appearance

허영 ( Young Her ) , 함지은 ( Ji Eun Hahm ) , 이진용 ( Jin Yong Lee ) , 이상렬 ( Sang Yeul Lee ) , 김상석 ( Sang Seok Kim )
  • : 대한피부과학회
  • : 대한피부과학회지 56권5호
  • : 연속간행물
  • : 2018년 06월
  • : 329-332(4pages)
피인용수 : 20건

(자료제공: 네이버학술정보)

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Pilomatricoma or calcifying epithelioma of Malherbe is a benign tumor originating from the matrix of hair follicles. Clinically, these tumors are classified as familial, perforating, multinodular, exophytic, anetodermic, bullous, and giant pilomatricomas. The bullous variety is observed only in 3 to 6% of cases. Furthermore, multiple pilomatricomas are rare and are usually associated with genetic disorders. To date, only 13 cases of bullous pilomatricoma and 8 cases of multiple pilomatricomas have been reported in Korean dermatologic literature. Among these cases, no case of multiple bullous pilomatricomas has been reported. This report describes a 23-year-old healthy man who was diagnosed with multiple pilomatricomas with bullous features, based on clinical and histopathological findings. (Korean J Dermatol 2018;56(5):329∼332)

UCI(KEPA)

I410-ECN-0102-2018-500-004089750

간행물정보

  • : 의약학분야  > 피부과학
  • : KCI등재
  • : SCOPUS
  • : 월간
  • : 0494-4739
  • :
  • : 학술지
  • : 연속간행물
  • : 1960-2020
  • : 9336


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1한국인 재색 피부병(Ashy Dermatosis) 74례의 임상 및 조직학적 특징 분석

저자 : 김나희 ( Na Hee Kim ) , 윤숙정 ( Sook Jung Yun ) , 이지범 ( Jee-bum Lee ) , 김성진 ( Seong-jin Kim ) , 이승철 ( Seung-chul Lee ) , 원영호 ( Young Ho Won )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 301-307 (7 pages)

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Background: Ashy dermatosis is a disorder of pigmentation, characterized by asymptomatic symmetric blue-graycolored macules of unknown pathophysiology.
Objective: Our aim was to evaluate ashy dermatosis in Koreans and to describe its clinical and histopathological features.
Methods: Medical records, photographs, and biopsy specimens obtained from 74 patients were assessed.
Results: Of the 74 patients, 38 were men and 36 were women. Clinically, most patients showed lesions on the trunk (83.8%), followed by the extremities (44.6%). At the time of the mean age was 29.9 years, and disease duration was 18.4 months before the institution. We tentatively classified the lesions into the following 3 groups: generalized confluent, generalized macular, and localized type. Clinically, the most common lesion was the generalized macular type (67.6%). Peripheral erythematous borders or concomitant erythematous lesions were observed in 18 patients (24.3%). Histopathologically, the lesions showed perivascular inflammation, dermal melanophages, and pigmentary incontinence.
Conclusion: Our study classified ashy dermatosis into 3 groups, and this categorization may contribute to a better understanding of ashy dermatosis. (Korean J Dermatol 2018;56(5):301∼307)

2한국인 건선관절염 환자의 임상적 특징과 치료양상에 대한 후향적 단일기관 연구

저자 : 이민석 ( Minseok Lee ) , 이재원 ( Jae Won Lee ) , 김태균 ( Tae-gyun Kim ) , 이민걸 ( Min-geol Lee )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 308-313 (6 pages)

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Background: Psoriatic arthritis (PsA) is a seronegative inflammatory arthritis associated with psoriasis. The prevalence of PsA varies across different countries, and a few previous studies have reported that 9∼17% of Korean patients with psoriasis present with PsA. However, limited data are available regarding the clinical features and treatment of Korean patients with PsA.
Objective: To evaluate the clinical features of Korean patients with PsA and the treatment modalities used in the real-world setting.
Methods: This study was a retrospective single-center study. We analyzed 101 Korean patients who had been diagnosed with PsA based on the Classification Criteria for Psoriatic Arthritis (CASPAR). We reviewed the patients' medical records, Psoriasis Area and Severity Index (PASI) score, body surface area (BSA), manifestation pattern of PsA, and treatment course.
Results: Our study included 101 patients. The mean age was 50.7 years. The mean PASI score was 8.6, and the mean BSA was 11.5%. Spondylitis was the most common manifestation (40.6%). In most patients, psoriatic lesions preceded the onset of PsA (57.4%). Psoriasis and PsA occurred simultaneously in 32.7%, and PsA developed prior to psoriasis in 9.9% of patients. The administration of nonsteroidal anti-inflammatory drugs (NSAIDs) was the most commonly utilized treatment strategy (82.2%), followed by the use of methotrexate and sulfasalazine. Twenty-two patients were treated with biologics with favorable efficacy.
Conclusion: Spondylitis was the most common manifestation in patients. NSAIDs, methotrexate and sulfasalazine were the drugs most commonly used to treat Korean patients with PsA. Dermatologists should be mindful of this entity, and during history taking at the patient's initial visit, those with psoriasis should be asked, “Do you have any pain or swelling of joints?” to ensure early diagnosis of PsA. (Korean J Dermatol 2018;56(5):308∼313)

3피부과로 협진의뢰된 입원환자의 약진에 대한 임상적 고찰

저자 : 이민영 ( Min Young Lee ) , 변지연 ( Ji Yeon Byun ) , 최혜영 ( Hae Young Choi ) , 최유원 ( You Won Choi )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 314-321 (8 pages)

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Background: Drug eruptions are common in hospitalized patients. Rapid and accurate diagnosis is essential but often difficult.
Objective: This study defined the clinical features and causative drugs among inpatients presenting with drug eruptions.
Methods: We retrospectively analyzed the clinical and laboratory data of inpatients who sought consultations with the Dermatology Department for a diagnosis of drug eruptions.
Results: A total of 228 patients were diagnosed with drug eruptions, and this study included 139 patients. The highest incidence of drug eruptions was observed in patients in their 50s (22.3%). The most common latent period was up to 1 week (57.6%). The most common drug eruptions were exanthematous eruptions (59.7%), acneiform eruptions (10.8%), and urticaria (9.3%). The most common causative drugs were antibiotics (53.2%), followed by anticancer drugs (19.4%), and contrast media (6.5%). Laboratory abnormalities included eosinophilia (15.8%), abnormal liver function tests (7.9%), leukopenia (4.3%), an elevated serum creatinine level (2.2%), and leukocytosis (0.7%).
Conclusion: In descending order, the most frequent drug eruptions were exanthematous eruptions, acneiform eruptions, and urticaria, and the most common causative drugs were antibiotics, anticancer agents, and contrast media. Prompt diagnosis and discontinuation of the causative drug are important in this context. Clinicians should be aware of cutaneous adverse drug reactions. (Korean J Dermatol 2018;56(5):314∼321)

4콜히친으로 치료한 성인에서의 재발성 특발성 호중구성 한선염 1예

저자 : 박지현 ( Ji Hyun Park ) , 천승현 ( Seung Hyun Chun ) , 김보영 ( Bo Young Kim ) , 유화정 ( Hwa Jung Ryu )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 322-324 (3 pages)

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Idiopathic neutrophilic eccrine hidradenitis is usually observed in healthy children with tender erythematous nodules on the soles or palms. We report a case of a 26-year-old man with a painful erythematous swollen patch on both hands and feet. His symptom recurred once monthly over 2 years; thus, he visited Orthopedics. However, no bony abnormality was identified. We performed a skin biopsy on an erythematous indurated patch on his right sole. Histopathological findings indicated neutrophilic eccrine hidradenitis. After 2 weeks of treatment with oral colchicine, his symptom resolved, and no relapses were observed during follow-up. Only a few case reports describe idiopathic neutrophilic eccrine hidradenitis in adults, which is not associated with malignant hematological disease, solid cancer, and chemotherapy. Conventional treatment comprises bed-rest and the administration of topical steroids. Colchicine can be a good treatment option for adults with severe or recurrent idiopathic neutrophilic eccrine hidradenitis. (Korean J Dermatol 2018;56(5):322∼324)

5베체트병과 동반된 심부정맥 혈전증 1예

저자 : 안혜진 ( Hye-jin Ahn ) , 신은재 ( Eun-jae Shin ) , 곽민재 ( Min-jae Gwak ) , 정기헌 ( Ki-heon Jeong ) , 이무형 ( Mu-hyoung Lee )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 325-328 (4 pages)

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Behcet's disease is a multisystem inflammatory disorder with a chronic relapsing course. It is considered a nonspecific systemic vasculitis involving both, venous and arterial circulation. Although lower extremity vein thrombosis (LEVT) is one of the most common manifestations of vascular involvement, a few cases are reported in the literature and to our knowledge, and only 2 cases were reported in Korea. We report a case of a 40-year-old Korean man with localized erythematous macules and patches on both lower extremities with a marked painful swelling on the right leg. The patient reported a history of similar lesions 10 years prior to presentation and also a history of recurrent aphthous oral ulcerations. Based on phlebographic findings of old LEVT in the right femoral vein, the patient was diagnosed with Behcet's disease associated with LEVT. (Korean J Dermatol 2018;56(5):325∼ 328)

6수포형이 동반된 다발성 모기질종

저자 : 허영 ( Young Her ) , 함지은 ( Ji Eun Hahm ) , 이진용 ( Jin Yong Lee ) , 이상렬 ( Sang Yeul Lee ) , 김상석 ( Sang Seok Kim )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 329-332 (4 pages)

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Pilomatricoma or calcifying epithelioma of Malherbe is a benign tumor originating from the matrix of hair follicles. Clinically, these tumors are classified as familial, perforating, multinodular, exophytic, anetodermic, bullous, and giant pilomatricomas. The bullous variety is observed only in 3 to 6% of cases. Furthermore, multiple pilomatricomas are rare and are usually associated with genetic disorders. To date, only 13 cases of bullous pilomatricoma and 8 cases of multiple pilomatricomas have been reported in Korean dermatologic literature. Among these cases, no case of multiple bullous pilomatricomas has been reported. This report describes a 23-year-old healthy man who was diagnosed with multiple pilomatricomas with bullous features, based on clinical and histopathological findings. (Korean J Dermatol 2018;56(5):329∼332)

7두 가지 아형의 한공각화증이 공존하면서 악성 변환이 발생한 증례

저자 : 박형진 ( Hyung-jin Park ) , 임준혁 ( June-hyuck Yim ) , 김태인 ( Tae In Kim ) , 정기헌 ( Ki-heon Jeong ) , 이무형 ( Mu-hyoung Lee ) , 신민경 ( Min Kyung Shin )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 333-337 (5 pages)

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The rate of malignant transformation in porokeratosis (PK) lesions is approximately 7.5%, and linear PK demonstrates the highest rate of malignancy. An 83-year-old woman presented with a rapidly enlarging mass on her left arm. Variably sized erythematous scaly patches were scattered across the left half of her trunk and arm. Additionally, generalized variably sized brownish annular patches with a hyperkeratotic outer ring were observed on her face, trunk and bilateral arms. A skin biopsy was performed on 3 lesions―a yellowish to erythematous appearing mass, an erythematous scaly patch, and a brownish annular patch. Histopathological evaluation of these 3 lesions revealed squamous cell carcinoma, actinic keratosis, and PK, respectively. The final diagnosis was disseminated superficial PK with linear PK on the left side of the body, and actinic keratosis and squamous cell carcinoma confined to the linear PK lesions. We report a case which represents the progressive and stepwise malignant transformation of PK into squamous cell carcinoma. (Korean J Dermatol 2018;56(5):333∼337)

8진행성 체모양 대상포진모양 과색소침착증: 증례보고와 문헌고찰

저자 : 이수경 ( Soo Kyung Lee ) , 서중헌 ( Joong Heon Suh ) , 김명신 ( Myoung Shin Kim ) , 이운하 ( Un Ha Lee )

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 338-342 (5 pages)

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Progressive cribriform and zosteriform hyperpigmentation (PCZH) is a distinctive pigmentary disorder observed along the lines of Blaschko. Clinically, the lesions appear as uniformly tan, cribriform macular hyperpigmentation with a zosteriform distribution, without a history of rash, injury, inflammation, or other associated cutaneous or internal abnormalities. Histopathological specimens show increased melanin pigmentation in the basal cell layer with a complete absence of nevus cells. We report 8 cases of PCZH and review the literature on this peculiar disorder. (Korean J Dermatol 2018;56(5):338∼342)

9펀치 피부 생검 후 발생한 하지의 림프관 손상 1예

저자 : 김창민 , 김일환

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 343-344 (2 pages)

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10회전피판술로 재건한 외비공턱의 기저세포암 1예

저자 : 박은정 , 조민결 , 유지숙 , 김민수 , 주민숙 , 최광현

발행기관 : 대한피부과학회 간행물 : 대한피부과학회지 56권 5호 발행 연도 : 2018 페이지 : pp. 344-345 (2 pages)

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12
주제별 간행물
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대한화장품학회지(J. Soc. Cosmet. Scientists Korea)
46권 1호 ~ 46권 1호

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58권 3호 ~ 58권 3호

KCI등재 SCI SCOUPUS

Annals of Dermatology
32권 2호 ~ 32권 2호

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대한피부과학회지
58권 2호 ~ 58권 2호

KCI등재

대한화장품학회지(J. Soc. Cosmet. Scientists Korea)
45권 4호 ~ 45권 4호

KCI등재 SCI SCOUPUS

Annals of Dermatology
32권 1호 ~ 32권 1호

KCI등재 SCOUPUS

대한피부과학회지
58권 1호 ~ 58권 1호

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대한피부과학회지
57권 10호 ~ 57권 10호

프로그램북(구 초록집)
71권 1호 ~ 71권 1호

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57권 9호 ~ 57권 9호

프로그램북(구 초록집)
71권 2호 ~ 71권 2호

KCI등재 SCI SCOUPUS

Annals of Dermatology
31권 6호 ~ 31권 6호

프로그램북(구 초록집)
71권 2호 ~ 71권 2호

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31권 6호 ~ 31권 6호

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45권 3호 ~ 45권 3호

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57권 8호 ~ 57권 8호

KCI등재 SCI SCOUPUS

Annals of Dermatology
31권 5호 ~ 31권 5호

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21권 1호 ~ 21권 1호

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57권 7호 ~ 57권 7호

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57권 6호 ~ 57권 6호
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