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Melanoma m (zero): diagnosis and therapy. 黑色素瘤 m(0):诊断和治疗。
Pub Date : 2013-04-11 Print Date: 2013-01-01 DOI: 10.1155/2013/616170
Marco Rastrelli, Mauro Alaibac, Roberto Stramare, Vanna Chiarion Sileni, Maria Cristina Montesco, Antonella Vecchiato, Luca Giovanni Campana, Carlo Riccardo Rossi

This paper reviews the epidemiology, diagnosis, and treatment of M zero cutaneous melanoma including the most recent developments. This review also examined the main risk factors for melanoma. Tumor thickness measured according to Breslow, mitotic rate, ulceration, and growth phase has the greatest predictive value for survival and metastasis. Wide excision of the primary tumor is the only potentially curative treatment for primary melanoma. The sentinel node biopsy must be performed on all patients who have a primary melanoma with a Breslow thickness > 1 mm, or if the melanoma is from 0,75 mm to 1 mm thick but it is ulcerated and/or the mitotic index is ≥1. Total lymph node dissection consists in removing the residual lymph nodes in patients with positive sentinel node biopsy, or found positive on needle aspiration biopsy, without radiological evidence of spread. Isolated limb perfusion and isolated limb infusion are employed in patients within transit metastases with a rate of complete remission in around 50% and 38% of cases. Electrochemotherapy is mainly indicated for palliation in cases of metastatic disease, though it may sometimes be useful to complete isolated limb perfusion. The only agent found to affect survival as an adjuvant treatment is interferon alpha-2. Adjuvant radiotherapy improves local control of melanoma in patients at a high risk of recurrence after lymph node dissection.

本文回顾了 M 零皮肤黑色素瘤的流行病学、诊断和治疗,包括最新进展。这篇综述还研究了黑色素瘤的主要风险因素。根据 Breslow、有丝分裂率、溃疡和生长期测量的肿瘤厚度对生存和转移具有最大的预测价值。广泛切除原发肿瘤是唯一可能治愈原发性黑色素瘤的治疗方法。如果原发黑色素瘤的布氏厚度大于 1 毫米,或者黑色素瘤的厚度在 0.75 毫米至 1 毫米之间,但已经溃烂和/或有丝分裂指数≥1,则必须对所有患者进行前哨活检。 对于前哨活检阳性或针吸活检阳性但无放射学扩散证据的患者,全淋巴结清扫术包括切除残余淋巴结。对于有转移灶的患者,可采用孤立肢体灌注和孤立肢体输注,完全缓解率分别为 50%和 38%。电化学疗法主要用于缓解转移性疾病,但有时也可用于完成孤立肢体灌注。作为辅助治疗,唯一能影响存活率的药物是干扰素α-2。对于淋巴结清扫术后复发风险较高的患者,辅助放疗可改善黑色素瘤的局部控制。
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引用次数: 0
Possible mechanisms by which topical 5-Fluorouracil and dermabrasion could induce pigment spread in vitiligo skin: an experimental study. 局部 5-氟尿嘧啶和磨皮诱导白癜风皮肤色素扩散的可能机制:一项实验研究。
Pub Date : 2013-04-09 Print Date: 2013-01-01 DOI: 10.1155/2013/852497
Y Gauthier, T Anbar, S Lepreux, M Cario-André, L Benzekri

The combination of skin ablation and 5-Fluorouracil (5-FU) ointment was previously tried in the treatment of vitiligo, and good results were specifically reported in glabrous skin without follicular melanocyte reservoirs. Methods. This study was carried out on the skins of seven guinea pigs: three were treated with mechanical dermabrasion plus topical 5-FU in an achromic area contiguous to a pigmented area; two were treated by only dermabrasion in a similar area; and two were treated by topical 5-FU alone. Clinical, histological, and ultrastructural studies were performed over two months. Results. In guinea pigs treated with dermabrasion plus 5-FU, we observed firstly a delay of wound healing with an obvious inflammatory reaction, and, after two months, evident pigment spread from the pigmented into the achromic area. After six months, we noticed black hair regrowing in the achromic area. Pigment spread was not seen in the guinea pigs skin treated by either dermabrasion or topical 5-FU. We suggest that the inflammatory mediators and enzymes (metalloproteinases), which are locally released over a long time, could stimulate and facilitate melanocyte proliferation and migration through the enlarged intercellular spaces of the epidermis. This sequence of events may be applied to vitiligo patients treated with 5-FU on ablated lesions.

以前曾尝试过皮肤消融术和 5-氟尿嘧啶(5-FU)软膏联合治疗白癜风,特别是在无毛囊黑色素细胞储库的无毛皮肤上取得了良好效果。研究方法这项研究是在七只豚鼠的皮肤上进行的:三只豚鼠在与色素沉着区相邻的失色区接受了机械磨皮加外用 5-FU 的治疗;两只豚鼠只在类似区域接受了磨皮治疗;两只豚鼠只接受了外用 5-FU 的治疗。临床、组织学和超微结构研究历时两个月。研究结果在接受磨皮加 5-FU 治疗的豚鼠身上,我们首先观察到伤口愈合延迟,并伴有明显的炎症反应。六个月后,我们发现消色区域重新长出黑色毛发。在采用磨皮或外用 5-FU 治疗的豚鼠皮肤上,均未发现色素扩散。我们认为,长期在局部释放的炎症介质和酶(金属蛋白酶)可刺激和促进黑色素细胞增殖,并通过表皮扩大的细胞间隙迁移。这一系列事件可能适用于在消融皮损上使用 5-FU 治疗的白癜风患者。
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引用次数: 0
Dermoscopic features of facial pigmented skin lesions. 面部色素皮损的皮肤镜特征。
Pub Date : 2013-01-01 Epub Date: 2013-02-03 DOI: 10.1155/2013/546813
Yana Goncharova, Enas A S Attia, Khawla Souid, Inna V Vasilenko

Four types of facial pigmented skin lesions (FPSLs) constitute diagnostic challenge to dermatologists; early seborrheic keratosis (SK), pigmented actinic keratosis (AK), lentigo maligna (LM), and solar lentigo (SL). A retrospective analysis of dermoscopic images of histopathologically diagnosed clinically-challenging 64 flat FPSLs was conducted to establish the dermoscopic findings corresponding to each of SK, pigmented AK, LM, and SL. Four main dermoscopic features were evaluated: sharp demarcation, pigment pattern, follicular/epidermal pattern, and vascular pattern. In SK, the most specific dermoscopic features are follicular/epidermal pattern (cerebriform pattern; 100% of lesions, milia-like cysts; 50%, and comedo-like openings; 37.50%), and sharp demarcation (54.17%). AK and LM showed a composite characteristic pattern named "strawberry pattern" in 41.18% and 25% of lesions respectively, characterized by a background erythema and red pseudo-network, associated with prominent follicular openings surrounded by a white halo. However, in LM "strawberry pattern" is widely covered by psewdonetwork (87.5%), homogenous structureless pigmentation (75%) and other vascular patterns. In SL, structureless homogenous pigmentation was recognized in all lesions (100%). From the above mentioned data, we developed an algorithm to guide in dermoscopic features of FPSLs.

四种类型的面部色素皮损(FPSLs)构成了皮肤科医生的诊断挑战;早期脂溢性角化病(SK)、色素光化性角化病(AK)、恶性黄斑(LM)和太阳性黄斑(SL)。回顾性分析64例经组织病理学诊断具有临床挑战性的扁平FPSLs的皮肤镜图像,以确定SK、色素AK、LM和SL各自对应的皮肤镜结果。评估四个主要的皮肤镜特征:清晰的界限、色素模式、滤泡/表皮模式和血管模式。在SK,最具体的皮肤镜特征是滤泡/表皮型(脑状型;100%病变,粟粒样囊肿;50%,粉刺样开口;37.50%),边界分明(54.17%)。AK和LM分别在41.18%和25%的病变中表现为复合特征模式,称为“草莓模式”,其特征为背景红斑和红色伪网络,伴有突出的滤泡开口,周围有白色晕。然而,在LM中,“草莓纹”被假网(87.5%)、均匀无结构色素沉着(75%)和其他维管纹广泛覆盖。在SL中,所有病变均可见无结构的均匀色素沉着(100%)。根据上述数据,我们开发了一种算法来指导FPSLs的皮肤镜特征。
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引用次数: 34
Sentinel lymph node biopsy in patients with thick primary cutaneous melanoma: patterns of use and underuse utilizing a population-based model. 原发性厚皮肤黑色素瘤患者的前哨淋巴结活检:利用基于人群的模型的使用模式和未充分使用。
Pub Date : 2013-01-01 Epub Date: 2013-01-10 DOI: 10.1155/2013/315609
Steve R Martinez, Dhruvil R Shah, Anthony D Yang, Robert J Canter, Emanual Maverakis

Background. Sentinel lymph node biopsy (SLNB) for thick cutaneous melanoma is supported by national guidelines. We report on factors associated with the use and underuse of SLNB for thick primary cutaneous melanoma. Methods. The Surveillance, Epidemiology, and End Results database was queried for patients who underwent surgery for thick primary cutaneous melanoma from 2004 to 2008. We used multivariate logistic regression models to predict use of SLNB. Results. Among 1,981 patients, 833 (41.8%) did not undergo SLNB. Patients with primary melanomas of the arm (OR 2.07, CI 1.56-2.75; P < 0.001), leg (OR 2.40, CI 1.70-3.40; P < 0.001), and trunk (OR 1.82, CI 1.38-2.40; P < 0.001) had an increased likelihood of receiving a SLNB, as did those with desmoplastic histology (OR 1.47, CI 1.11-1.96; P = 0.008). A decreased likelihood of receiving SLNB was noted for advancing age ≥ 60 years (age 60 to 69: OR 0.58, CI 0.33-0.99, P = 0.047; age 70 to 79: OR 0.32, CI 0.19-0.54, P < 0.001; age 80 or more: OR 0.10, CI 0.06-0.16, P < 0.001) and unknown race/ethnicity (OR 0.21, CI 0.07-0.62; P = 0.005). Conclusions. In particular, elderly patients are less likely to receive SLNB. Further research is needed to assess whether use of SLNB in this population is detrimental or beneficial.

背景。前哨淋巴结活检(SLNB)厚皮肤黑色素瘤是支持国家指南。我们报道与SLNB治疗原发性厚皮肤黑色素瘤的使用和未充分使用相关的因素。方法。对2004年至2008年接受过原发性厚皮肤黑色素瘤手术的患者的监测、流行病学和最终结果数据库进行了查询。我们使用多元逻辑回归模型来预测SLNB的使用。结果。1981例患者中,833例(41.8%)未行SLNB。手臂原发性黑色素瘤患者(OR 2.07, CI 1.56-2.75;P < 0.001),组(OR 2.40, CI 1.70-3.40;P < 0.001),主干(OR 1.82, CI 1.38-2.40;P < 0.001)的患者接受SLNB的可能性增加,有结缔组织增生组织学的患者也是如此(OR 1.47, CI 1.11-1.96;P = 0.008)。年龄≥60岁的患者接受SLNB的可能性降低(60 - 69岁:OR 0.58, CI 0.33-0.99, P = 0.047;70 ~ 79岁:OR 0.32, CI 0.19 ~ 0.54, P < 0.001;80岁或以上:or 0.10, CI 0.06-0.16, P < 0.001)和未知种族/民族(or 0.21, CI 0.07-0.62;P = 0.005)。结论。特别是老年患者接受SLNB的可能性较小。需要进一步的研究来评估在这一人群中使用SLNB是有害还是有益。
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引用次数: 5
Adjuvant treatment of melanoma. 黑色素瘤的辅助治疗。
Pub Date : 2013-01-01 Epub Date: 2013-02-17 DOI: 10.1155/2013/545631
J A Moreno Nogueira, M Valero Arbizu, R Pérez Temprano

Melanomas represent 4% of all malignant tumors of the skin, yet account for 80% of deaths from skin cancer.While in the early stages patients can be successfully treated with surgical resection, metastatic melanoma prognosis is dismal. Several oncogenes have been identified in melanoma as BRAF, NRAS, c-Kit, and GNA11 GNAQ, each capable of activating MAPK pathway that increases cell proliferation and promotes angiogenesis, although NRAS and c-Kit also activate PI3 kinase pathway, including being more commonly BRAF activated oncogene. The treatment of choice for localised primary cutaneous melanoma is surgery plus lymphadenectomy if regional lymph nodes are involved. The justification for treatment in addition to surgery is based on the poor prognosis for high risk melanomas with a relapse index of 50-80%. Patients included in the high risk group should be assessed for adjuvant treatment with high doses of Interferon- α 2b, as it is the only treatment shown to significantly improve disease free and possibly global survival. In the future we will have to analyze all these therapeutic possibilities on specific targets, probably associated with chemotherapy and/or interferon in the adjuvant treatment, if we want to change the natural history of melanomas.

黑色素瘤占所有皮肤恶性肿瘤的4%,但却占癌症死亡人数的80%。虽然在早期阶段,患者可以通过手术切除成功治疗,但转移性黑色素瘤的预后却令人沮丧。黑色素瘤中的几种致癌基因已被鉴定为BRAF、NRAS、c-Kit和GNA11-GNAQ,每种都能够激活MAPK途径,从而增加细胞增殖并促进血管生成,尽管NRAS和c-Kit也激活PI3激酶途径,包括更常见的BRAF激活的致癌基因。局部原发性皮肤黑色素瘤的治疗选择是手术加淋巴结切除术(如果涉及区域淋巴结)。除手术外进行治疗的理由是,复发指数为50-80%的高危黑色素瘤预后不佳。应评估高危组患者是否接受高剂量干扰素-α2b的辅助治疗,因为这是唯一一种能显著提高无病生存率和可能的全球生存率的治疗方法。未来,如果我们想改变黑色素瘤的自然史,我们必须分析所有这些针对特定靶点的治疗可能性,可能与辅助治疗中的化疗和/或干扰素有关。
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引用次数: 8
Effect of Infliximab on the UVB-Induced Apoptosis of Keratinocytes Infected by HPV38 E6/E7. 英夫利昔单抗对uvb诱导的HPV38 E6/E7感染角化细胞凋亡的影响
Pub Date : 2013-01-01 Epub Date: 2013-02-25 DOI: 10.1155/2013/907189
François Aubin, Tarik Gheit, Jean Luc Prétet, Massimo Tommasino, Christiane Mougin

The question of the effect of anti-TNF-alpha in skin carcinogenesis is especially relevant in view of the increased use of these drugs for the treatment of autoinflammatory immune diseases. Since ultraviolet radiation and human papillomavirus are involved in skin carcinogenesis, we wished to investigate the effect of TNF-alpha antagonists on the UVB-induced apoptosis of keratinocytes infected by HPV38. Our results indicate that anti-TNF agent, infliximab, does not contribute to the survival of HPV38-transduced keratinocytes with UVB-induced DNA damages.

鉴于越来越多地使用抗tnf - α药物治疗自身炎症性免疫疾病,抗tnf - α在皮肤癌变中的作用问题尤为重要。由于紫外线辐射和人乳头瘤病毒参与了皮肤癌的发生,我们希望研究tnf - α拮抗剂对uvb诱导的HPV38感染的角质形成细胞凋亡的影响。我们的研究结果表明,抗肿瘤坏死因子英夫利昔单抗对uvb诱导的DNA损伤的hpv38转导的角质形成细胞的存活没有贡献。
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引用次数: 1
Acquired melanonychia in chilean patients with essential thrombocythemia treated with hydroxyurea: a report of 7 clinical cases and review of the literature. 接受羟基脲治疗的智利原发性血小板增多症患者的后天性黑变病:7 个临床病例的报告和文献综述。
Pub Date : 2013-01-01 Epub Date: 2013-02-07 DOI: 10.1155/2013/325246
Nigel P Murray, Pablo Tapia, Jose Porcell, Maximiliano Echavarria, Hernán Suazo

Longitudinal melanonychia has been associated with a range of drugs, especially chemotherapeutic agents. We report 7 cases of melanonychia associated with the use of hydroxycarbamide for essential thrombocythemia. Of a patient population of 27, 7 (26%) developed melanonychia over a period of 2-7 years, and was not dose dependent. The high incidence of melanonychia in Chilean patients may be in part due to their Hispanic descent or to the high levels of UV radiation found in Santiago.

纵向黑变病与一系列药物有关,尤其是化疗药物。我们报告了 7 例因使用羟基卡巴酰胺治疗原发性血小板增多症而导致的黑斑。在 27 例患者中,有 7 例(26%)在 2-7 年的时间里出现了黑斑,且与剂量无关。智利患者的黑斑病发病率较高,部分原因可能是他们是西班牙裔或圣地亚哥的紫外线辐射较强。
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引用次数: 0
Effectiveness of keishibukuryogan on chronic-stage lichenification associated with atopic dermatitis. keishibukuryogan治疗与特应性皮炎相关的慢性地衣变的疗效。
Pub Date : 2012-01-01 Epub Date: 2012-11-14 DOI: 10.5402/2012/158598
Megumi Mizawa, Teruhiko Makino, Hiroaki Hikiami, Yutaka Shimada, Tadamichi Shimizu

Atopic dermatitis (AD) is a common inflammatory skin disease with recurring episodes of itching and a chronic relapsing course. Keishibukuryogan (KBG) is a traditional herbal medicine, composed of five kinds of medical plants and has been administered to patients with blood stagnation in Japan. This study investigated the effect of KBG on the disease activity in AD (n = 45) patients. AD patients were administered KBG for 4 to 6 weeks in addition to their prescribed medications. The results showed that the SCORAD index and VAS score were significantly decreased after the administration of KBG (P < 0.01). KBG also decreased the serum LDH level significantly (P < 0.01). The global assessment of the clinical response in SCORAD index showed that 88.5% of the patients with moderate improvement to excellent response (n = 26) had a high lichenification score (lichenification score ≥2 in SCORAD). On the other hand, only 42.1% of the patients with no improvement to mild improvement (n = 19) had a high lichenification score. Furthermore, long-term administration of KBG for 9-67 weeks showed a marked improvement in patients with a high lichenification score. Therefore, KBG was found to be effective against AD, particularly in cases presenting with lichenified lesions.

特应性皮炎(AD)是一种常见的炎症性皮肤病,反复发作的瘙痒和慢性复发的过程。Keishibukuryogan (KBG)是一种传统的草药,由五种药用植物组成,在日本被用于治疗血瘀患者。本研究探讨了KBG对AD患者疾病活动性的影响(n = 45)。AD患者在服用处方药物的同时服用KBG 4 - 6周。结果显示,给予KBG后,患者的SCORAD指数和VAS评分均显著降低(P < 0.01)。KBG显著降低了血清LDH水平(P < 0.01)。对SCORAD指数临床反应的整体评估显示,88.5%中度改善至极好缓解的患者(n = 26)的地衣化评分较高(SCORAD地衣化评分≥2)。另一方面,无改善至轻度改善的患者中仅有42.1% (n = 19)的地衣变评分较高。此外,长期服用KBG 9-67周,对地衣化评分高的患者有显著改善。因此,发现KBG对AD有效,特别是在出现地衣化病变的情况下。
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引用次数: 12
A comparative analysis of mast cell quantification in five common dermatoses: lichen simplex chronicus, psoriasis, lichen planus, lupus, and insect bite/allergic contact dermatitis/nummular dermatitis. 5种常见皮肤病:慢性单纯性地衣、牛皮癣、扁平地衣、狼疮和虫咬/过敏性接触性皮炎/钱币性皮炎肥大细胞定量的比较分析
Pub Date : 2012-01-01 Epub Date: 2012-02-01 DOI: 10.5402/2012/759630
Nikhil Patel, Amir Mohammadi, Ronald Rhatigan

There is a large body of literature demonstrating an important role of mast cells in adaptive and innate immunity. The distribution of mast cells in the skin varies in different parts of the body. It is well known that mast cells are important for effector functions of classic IgE-associated allergic disorders as well as in host defense against infective agents and influence the manifestation of autoimmune diseases. We aimed to quantify mast cells in five common dermatoses and compare them statistically with respect to the immunostains. We retrieved paraffin-embedded tissue sections from the archives of the Pathology Department at the UF, Jacksonville, for five cases with each of the above diagnosis from the last three years. We performed CD-117 and tolidine blue stains on each one of them. The presence or absence of mast cells was evaluated and quantified. We observed that, in the skin, mast cells are mainly located close to the vessels, smooth muscle cells, hair follicles, and nerve ending. Our study showed that the mast cell distribution pattern is different across the two methods of staining for the five aforesaid dermatoses. The other important observation was the dendritic morphology of the mast cells.

有大量的文献证明肥大细胞在适应性免疫和先天免疫中的重要作用。肥大细胞在皮肤中的分布在身体的不同部位是不同的。众所周知,肥大细胞在典型的ige相关过敏性疾病的效应功能以及宿主对感染因子的防御和影响自身免疫性疾病的表现中发挥重要作用。我们的目的是量化五种常见皮肤病的肥大细胞,并将它们与免疫染色进行统计比较。我们从杰克逊维尔佛罗里达大学病理科的档案中检索石蜡包埋组织切片,在过去三年中分别有上述诊断的五个病例。我们对他们进行了CD-117和甲苯胺蓝染色。肥大细胞的存在与否被评估和量化。我们观察到,在皮肤中,肥大细胞主要分布在血管、平滑肌细胞、毛囊和神经末梢附近。我们的研究表明,在上述五种皮肤病的两种染色方法中,肥大细胞分布模式是不同的。另一个重要的观察结果是肥大细胞的树突形态。
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引用次数: 14
Papillon-lefèvre syndrome: a series of six cases in the same family. 左侧乳头状瘤综合征:同一家族6例。
Pub Date : 2012-01-01 Epub Date: 2012-12-03 DOI: 10.5402/2012/139104
Ali Kord Valeshabad, Abdolmotaleb Mazidi, Reza Kord Valeshabad, Elham Imani, Hadi Kord, Mohammad Koohkan, Zrynal Sayinar, Khalil Al-Talib

Papillon-Lefèvre syndrome (PLS) is a rare, autosomal recessive heterogeneous disorder, which is characterized by palmoplantar hyperkeratosis, early loss of primary and permanent teeth, and associated calcification of the dura mater. Herein we described six cases of PLS in the same family. In this series, six cases (two females and four males) with the mean age of 15.6 ± 10.4 years were recruited. Palmoplantar hyperkeratosis was detected in all of the cases, leading to a difficult and painful walking in two cases due to lesions on the soles. Skin lesions were sharply distinct from adjacent normal skin in all cases. Other skin lesions were located in the external malleolus (5/6), knee (4/6), elbow (4/6), toe and dorsal fingers (3/6), and the thighs (2/6). In three cases, all permanent teeth were exfoliated. In three others, no primary teeth remained. Severe gingivitis was observed in three patients. Radiologic study confirmed alveolar bone destruction in five cases. Delayed diagnosis and insufficient treatment of PLS patients can affect patient's life of by causing edentulism at a young age and may impose PLS patients to increased risk of social, psychological, and economical burdens.

乳突-左滴综合征(PLS)是一种罕见的常染色体隐性遗传性异质性疾病,其特征是掌跖角化过度,早期乳牙和恒牙脱落,以及相关的硬脑膜钙化。在此,我们描述了6例PLS在同一家庭。本研究共纳入6例患者(2女4男),平均年龄15.6±10.4岁。所有病例均发现掌足底角化过度,其中2例由于脚底病变导致行走困难和疼痛。所有病例的皮肤病变与邻近正常皮肤明显不同。其他皮损位于外踝(5/6)、膝关节(4/6)、肘部(4/6)、趾及指背(3/6)、大腿(2/6)。3例患者的恒牙全部脱落。另外三名患者没有乳牙。3例患者出现严重牙龈炎。影像学检查证实5例牙槽骨破坏。PLS患者诊断的延迟和治疗的不充分可能会导致年幼的牙齿发育,从而影响患者的生活,并可能使PLS患者增加社会、心理和经济负担的风险。
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引用次数: 10
期刊
ISRN Dermatology
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