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Multifocal squamous cell carcinoma arising in a Favre-Racouchot lesion - report of two cases and review of the literature. Favre-Racouchot病变引起的多灶性鳞状细胞癌——附两例报告并文献复习。
Pub Date : 2015-12-31 DOI: 10.3315/jdcr.2015.1215
Natalja E Leeuwis-Fedorovich, M. Starink, A. C. van der Wal
BACKGROUNDFavre-Racouchot syndrome (nodular cutaneous elastosis with cysts and comedones) is a cutaneous disease characterized by coexistence of cysts, comedones and elastotic nodules in actinically damaged skin, typically on the face. Ultraviolet radiation plays a significant role in the development of the disease. Unilateral lesions have been described.MAIN OBSERVATIONIn this report we present two cases of squamous cell carcinoma arising in a unilateral Favre-Racouchot plaque. Both patients, fair-skinned, elderly, with impaired immune function developed large, deep invasive tumors with perineural extension.CONCLUSIONSSquamous cell carcinomas of large size and prominent invasive growth developing in immunocompromised individuals carry poor prognosis with regard to recurrence rate and metastasis. Manifestations of malignancy as described in this report, indicate the importance of close follow-up of patients with Favre-Racouchot syndrome.
favre - racouchot综合征(结节性皮肤弹性变性伴囊肿和粉刺)是一种皮肤疾病,其特征是囊肿、粉刺和弹性结节在皮肤损伤中共存,通常发生在面部。紫外线辐射在这种疾病的发展中起着重要作用。单侧病变已被描述。主要观察:在本报告中,我们报告了两例发生于单侧Favre-Racouchot斑块的鳞状细胞癌。这两例患者,皮肤白皙,年龄大,免疫功能受损,发生大而深的侵袭性肿瘤,伴神经周围延伸。结论发生于免疫功能低下人群的鳞状细胞癌体积大且浸润性生长明显,其复发率和转移率预后较差。本报告中所描述的恶性肿瘤表现表明对Favre-Racouchot综合征患者进行密切随访的重要性。
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引用次数: 11
Delayed hypersensitivity reaction to intralesional triamcinolone acetonide following treatment for alopecia areata. Intradermal testing. 斑秃治疗后局部曲安奈德迟发性超敏反应。皮内试验。
Pub Date : 2015-12-31 DOI: 10.3315/jdcr.2015.1216
F. C. Kreeshan, P. Hampton
BACKGROUNDHypersensitivity reactions to intralesional corticosteroids are very rare and have been infrequently reported. Patch testing is considered the gold standard for diagnosing contact allergic dermatitis. However, intradermal testing is thought to be more accurate and sensitive in selected cases.MAIN OBSERVATIONWe describe a case of a delayed hypersensitivity reaction to intralesional triamcinolone acetonide following the treatment of alopecia areata. Patch testing to triamcinolone was negative but intradermal testing with a small volume of the same reagent elicited a strong reaction.CONCLUSIONSPatch testingmay be unsuccessful in detecting delayed reactions to intralesional corticosteroids. In such cases intradermal testing at a non-cosmetically sensitive sitemay be a useful diagnostic tool.
背景:局部皮质类固醇的超敏反应是非常罕见的,很少有报道。斑贴试验被认为是诊断接触性过敏性皮炎的金标准。然而,皮内检测被认为在某些情况下更为准确和敏感。主要观察:我们报告一例迟发性局部曲安奈德治疗斑秃后的超敏反应。膜片试验对曲安奈德阴性,皮内试验用小体积相同的试剂引起强烈反应。结论斑点试验不能很好地检测局部皮质类固醇的延迟反应。在这种情况下,在非美容敏感部位进行皮内检测可能是一种有用的诊断工具。
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引用次数: 4
Photoletter to the editor: Subcutaneous ciliated Mullerian cyst. 给编辑的照相信:皮下纤毛苗勒氏囊肿。
Pub Date : 2015-12-31 DOI: 10.3315/jdcr.2015.1218
Matthew Keisling, A. Marinovich, B. Burkey
Cutaneous ciliated cysts are benign lesions occurring primarily on the lower extremity of girls and young women. We present a case of a cutaneous ciliated Mullerian cyst arising in the lower leg of a 14-year-old girl, with brief discussion of etiology and diagnosis. This is a rare entity with approximately 50 cases in the literature.
皮肤纤毛囊肿是良性病变,主要发生在女孩和年轻妇女的下肢。我们提出一个14岁女孩小腿皮肤纤毛缪勒氏囊肿的病例,并简要讨论病因和诊断。这是一种罕见的实体,在文献中约有50例。
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引用次数: 2
Behçet's disease in black skin. A retrospective study of 50 cases in Dakar. 黑皮肤的behaperet病。对达喀尔50例病例的回顾性研究。
Pub Date : 2015-12-31 DOI: 10.3315/jdcr.2015.1213
M. Ndiaye, A. S. Sow, Abbaspour Valiollah, M. Diallo, A. Diop, R. Alaoui, B. Diatta, F. Ly, S. Niang, M. Dieng, A. Kane
INTRODUCTIONAlthough Behçet's disease is well-documented in Eastern populations, epidemiologic data in Sub-Saharan African population is scarce. The aim of this study was to define the epidemiologic and therapeutic aspects as well as clinical course of Behçet's disease in African black population.RESULTSThe study included 50 patients with Behçet's disease. The average age was 32 (18-67) years. A total of 31 patients were men and 19 were women. Two patients had a positive family history of Behçet's disease. The oral and genital aphthous lesions were present in 100% of patients. The pathergy test was positive in 16 patients (32%). Following skin conditions were observed: pseudofolliculitis in 15 patients (30%), acneiform papules in 6 patients (12%), erythema nodosum in 4 patients (8%) and leg ulcers in one patient. Ocular involvement was reported in 22 patients (44%) and joint involvement in 20 patients (40%). Neurological abnormalities were noted in 12 patients (24%). Gastrointestinal involvement with wide and deep ulcerations in the ileocecal region was observed in a patient. As treatment, a combination of oral corticosteroids and colchicine was used in 97% of our patients. Thalidomide was introduced in 3 patients and anticoagulation treatment in 19 patients. Clinical improvement was noted in 25 patients (50%), recurrence in 14 patients (28%) and 3 patients were lost to follow (6%).CONCLUSIONThe Behçet's disease is not uncommon in black skin and generally affects young adults. Severe aphthous ulcers of the oral cavity and genital area are the most consistent finding.
虽然behet病在东部人群中有充分的文献记载,但撒哈拉以南非洲人口的流行病学数据很少。本研究的目的是确定非洲黑人behaperet病的流行病学和治疗方面以及临床病程。结果本研究纳入了50例behaperet病患者。平均年龄32岁(18-67岁)。男性31例,女性19例。2例患者有behaperet病阳性家族史。100%的患者出现口腔和生殖器口疮病变。病理试验阳性16例(32%)。观察到以下皮肤状况:假性毛囊炎15例(30%),痤疮样丘疹6例(12%),结节性红斑4例(8%),腿部溃疡1例。眼部受累22例(44%),关节受累20例(40%)。12例(24%)患者出现神经系统异常。在一个病人观察到胃肠道受累与广泛和深的溃疡在回盲区。作为治疗,97%的患者使用口服皮质类固醇和秋水仙碱的组合。使用沙利度胺3例,抗凝治疗19例。临床改善25例(50%),复发14例(28%),失访3例(6%)。结论behaperet病在黑皮肤中并不少见,多见于青壮年。严重的口腔溃疡和生殖器区域是最一致的发现。
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引用次数: 21
Photoletter to the editor: Response of linear porokeratosis to photodynamic therapy in an 11-year-old girl. 致编辑:一名11岁女孩光动力疗法对线性骨质疏松症的反应。
Pub Date : 2015-12-31 DOI: 10.3315/jdcr.2015.1220
C. Garrido-Colmenero, R. Ruiz-Villaverde, E. Martínez-García, J. Aneiros-Fernández, J. Tercedor-Sánchez
Porokeratoses are a group of different entities that belong to the skin keratinization disorders. From the histological point of view the main and common characteristic of these disorders is the presence of compact parakeratotic columns known as cornoid lamellae. All varieties should be carefully treated and followed-up because of the risk of developing malignant epithelial tumors. We report the successful response to photodynamic therapy (PDT) in a pediatric patient diagnosed with linear porokeratosis.
多孔性角化病是一组属于皮肤角化疾病的不同实体。从组织学角度来看,这些疾病的主要和共同特征是存在紧密的角化不全柱,称为角膜片状。由于有发展为恶性上皮肿瘤的风险,所有品种都应仔细治疗和随访。我们报告成功响应光动力疗法(PDT)在儿科患者诊断为线性骨质疏松症。
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引用次数: 7
Cryptococcal panniculitis in a renal transplant recipient: case report and review of literature. 肾移植受者隐球菌性潘膜炎一例报告及文献复习。
Pub Date : 2015-09-30 DOI: 10.3315/jdcr.2015.1205
Sunil K Kothiwala, Mahesh Prajapat, Chhitar Mal Kuldeep, Arpita Jindal

Background: Cryptococcosis is a deep fungal infection caused by Cryptococcus neoformans. The infection usually involves the lungs, the central nervous system as well as the skin, the bones and the urinary tract. Immunocompromised individuals, including solid organ transplant recipients, are at higher risk for cryptococcal infections.

Main observations: We present a 40-year-old renal transplant recipient who developed a slightly painful, erythematous, indurated plaque on his thigh several years after a kidney transplant. Histopathology revealed cryptococcal panniculitis and cryptococcus neoformans subsequently grew from the tissue culture. There was no other systemic involvement.

Conclusion: The primary cutaneous form of cryptococcosis is extremely rare and early diagnosis and treatment is essential in view of possible dissemination and variable nonspecific clinical manifestations.

背景:隐球菌病是一种由新型隐球菌引起的深部真菌感染。感染通常涉及肺部、中枢神经系统以及皮肤、骨骼和泌尿道。免疫功能低下的个体,包括实体器官移植接受者,感染隐球菌的风险更高。主要观察:我们报告了一位40岁的肾移植受者,在肾移植几年后,他的大腿上出现了轻微的疼痛,红斑,硬化斑块。组织病理学显示组织培养后出现隐球菌性全身炎和新型隐球菌。没有其他系统性的介入。结论:原发性皮肤隐球菌病极为罕见,鉴于其可能的传播和多变的非特异性临床表现,早期诊断和治疗至关重要。
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引用次数: 9
Photoletter to the editor: Exogenous pigmentation after Diplopoda exposure leading to a dermatoscopic parallel ridge pattern on the plantar region. 给编辑的照相书:外源性色素沉着后,双足类暴露导致一个平行脊图案在足底区域的皮肤镜。
Pub Date : 2015-09-30 DOI: 10.3315/jdcr.2015.1209
Tainá Scalfoni Fracaroli, Ludmilla Queirós Miranda, Juan Piñeiro Maceira, Carlos Baptista Barcaui

The millipedes (also known as "gongolos") are arthropods characterized by a cylindrical body consisting of rings. When threatened, they release chemicals that can cause erythema and hyperpigmentation. We report the case of a patient who developed a darkened macule on the plantar region after stepping on a millipede. Dermatoscopic examination showed a parallel-ridge pattern, which is considered typical for acral melanoma. A detailed history was essential for the diagnosis, as the clinical and dermatoscopic features suggested a malignant melanocytic lesion.

千足虫是一种节肢动物,其特征是由环组成的圆柱形身体。当受到威胁时,它们会释放出能引起红斑和色素沉着的化学物质。我们报告的情况下,一个病人谁开发了一个黑暗的斑在足底地区踩了千足虫后。皮镜检查显示平行脊型,这被认为是典型的肢端黑色素瘤。详细的病史对诊断是必要的,因为临床和皮肤镜特征提示恶性黑素细胞病变。
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引用次数: 8
Photoletter to the editor: Topical 0.5% brimonidine gel to camouflage redness of immature scars. 给编辑的信:外用0.5%溴胺凝胶来掩盖未成熟疤痕的红肿。
Pub Date : 2015-09-30 DOI: 10.3315/jdcr.2015.1210
Markus Reinholz, Markus Heppt, Julia K Tietze, Thomas Ruzicka, Gerd G Gauglitz, Jürgen Schauber

Cutaneous scars develop as a result of a defective wound healing process. Scars are commonly visible as erythematous, sometimes disfiguring lesions which might be stigmatizing for the affected patient. Only a few therapies to improve the appearance of scars are available. Recently, brimonidine - a selective α2-receptor-agonist which causes vasoconstriction of small cutaneous vessels - was approved for the treatment of erythemato-telangiectatic rosacea. Topical brimonidine might also be helpful to improve redness of immature scars. Here we report on the effect of brimonidine 0.5% gel on a flat, erythematous scar in a 25-year-old female patient. Whitening of the scar could be observed immediately after application of brimonidine 0.5% gel and a good clinical result was observed within one hour. This effect lasted for up to three hours. We conclude that brimonidine 0.5% gel is a suitable topical therapy to reduce erythema in visible cutaneous scars.

皮肤疤痕是由于伤口愈合过程的缺陷而产生的。疤痕通常是可见的红斑,有时毁容的病变,这可能是受影响的病人的耻辱。只有几种治疗方法可以改善疤痕的外观。最近,溴莫尼定-一种选择性α2受体激动剂,可引起小皮肤血管收缩-被批准用于治疗红斑毛细血管扩张型酒痤疮。局部使用溴硝定也可能有助于改善未成熟疤痕的发红。在这里,我们报告0.5%溴莫尼定凝胶对25岁女性患者扁平红斑疤痕的影响。0.5%溴莫尼定凝胶敷后即刻可观察到瘢痕的增白,1小时内临床效果良好。这种效果持续了三个小时。我们认为0.5%溴莫尼定凝胶是一种合适的局部治疗方法,可以减少可见皮肤疤痕的红斑。
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引用次数: 3
Long-term ustekinumab therapy of psoriasis in patients with coexisting rheumatoid arthritis and Sjögren syndrome. Report of two cases and review of literature. 长期ustekinumab治疗并发类风湿关节炎和Sjögren综合征的银屑病患者。二例报告及文献复习。
Pub Date : 2015-09-30 DOI: 10.3315/jdcr.2015.1207
Maria Sole Chimenti, Marina Talamonti, Lucia Novelli, Miriam Teoli, Marco Galluzzo, Paola Triggianese, Roberto Perricone

Background: Inteleukin (IL)12 and IL23 are two main cytokines involved in the pathogenesis of immune-mediated disease. IL12 is produced by macrophages and B lymphocytes and mediates differentiation of Th1 lymphocytes, while IL23 is a pro-inflammatory cytokine essential for the differentiation of Th17 cells. Ustekinumab is a human monoclonal antibody directed against the p40 protein subunit shared by IL12 and IL23, therefore it blocks the signal transmission of both cytokines.

Main observations: We present two cases and discuss the long-term efficacy of ustekinumab as a treatment of psoriasis in patients affected by autoimmune diseases, rheumatoid arthritis and Sjögren's syndrome, who presented with severe psoriasis after anti-TNF treatment.

Conclusions: To the best of our knowledge, these are the first cases reported in the literature describing the long-term good efficacy of ustekinumab not only on paradoxical forms of psoriasis induced by anti-TNF-α drugs, but also on the articular involvement in a patient affected by RA and in a patient affected by Sjögren syndrome.

背景:白细胞介素(IL)12和IL23是参与免疫介导性疾病发病的两种主要细胞因子。il - 12由巨噬细胞和B淋巴细胞产生,介导Th1淋巴细胞的分化,而il - 23是Th17细胞分化所必需的促炎细胞因子。Ustekinumab是一种针对IL12和IL23共有的p40蛋白亚基的人单克隆抗体,因此它阻断这两种细胞因子的信号传递。主要观察:我们报告了两个病例,并讨论了ustekinumab治疗自身免疫性疾病、类风湿性关节炎和Sjögren综合征患者的牛皮癣的长期疗效,这些患者在抗tnf治疗后出现严重的牛皮癣。结论:据我们所知,这是文献中首次报道的病例,描述了ustekinumab不仅对抗tnf -α药物诱导的矛盾形式的牛皮癣有长期良好的疗效,而且对RA患者和Sjögren综合征患者的关节累及也有良好的疗效。
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引用次数: 11
Disseminated refractory pyoderma gangraenosum during an ulcerative colitis flare. Treatment with infliximab. 溃疡性结肠炎发作时弥散性难治性坏疽性脓皮病。英夫利昔单抗治疗。
Pub Date : 2015-09-30 DOI: 10.3315/jdcr.2015.1206
Vasiliki A Zampeli, Undine Lippert, Georgios Nikolakis, Evgenia Makrantonaki, Thrasivoulos G Tzellos, Ulf Krause, Christos C Zouboulis

Background: Pyoderma gangraenosum is an immune-mediated, inflammatory, neutrophilic dermatosis of unknown etiology, which represents one of the extraintestinal manifestations of inflammatory bowel disease. It is a rare disease that occurs in less than 1% of patients with inflammatory bowel disease and with the same ratio in patients with Crohn's disease and ulcerative colitis.

Main observations: A 36-year-old woman was diagnosed with ulcerative colitis 6 years before admission to our dermatology department with an acute disseminated pyoderma gangraenosum with mucosal involvement, during a flare of ulcerative colitis. Disease progression was interrupted by intravenous administration of the tumor necrosis factor-α inhibitor infliximab at 5 mg/kg at weeks 0, 2, and 6 (1st cycle) and every 8 weeks thereafter. Improvement of intestinal, skin and oral manifestations was evident already after the 1st cycle of treatment and has been maintained since (at least 16 months).

Conclusions: This case report is one of very few on disseminated pyoderma gangraenosum with oral involvement complicating ulcerative colitis, where infliximab was shown to have a rapid efficacy on skin, mucosal and bowel symptoms.

背景:坏疽性脓皮病是一种病因不明的免疫介导的炎症性中性粒细胞皮肤病,是炎症性肠病的肠外表现之一。这是一种罕见的疾病,在炎症性肠病患者中发病率不到1%,在克罗恩病和溃疡性结肠炎患者中发病率也不到1%。主要观察:一名36岁女性在溃疡性结肠炎发作期间,因急性弥散性坏疽性脓皮病累及粘膜,于入院前6年被诊断为溃疡性结肠炎。在第0、2和6周(第1周期)以及此后每8周静脉给予肿瘤坏死因子-α抑制剂英夫利昔单抗5mg /kg,以中断疾病进展。在第一个治疗周期后,肠道、皮肤和口腔症状的改善已经很明显,并且一直保持至今(至少16个月)。结论:本病例报告是为数不多的弥散性坏疽性脓皮病合并口腔累及溃疡性结肠炎病例之一,其中英夫利昔单抗对皮肤、粘膜和肠道症状有快速疗效。
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引用次数: 17
期刊
Journal of dermatological case reports
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