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| 1 | Pigmented purpuric dermatitis preceding the diagnosis of mycosis fungoidos by 24 years显示文摘 | Viseux V Schoenlaub P Cnudde F | 2003 | Dermatology2003，207，3： | 1 |
| 2 | Topical silver sulfadiazine-induced acute renal failure显示文摘 | Chaby G Viseux V Poulain J F | 2005 | Annales de Dermatologie et de Vénéréologie2005，，11： | 1 |
| 3 | Brain magnetic resonance imaging in patients with Cowden syndrome显示文摘 | Lok C Viseux V Avril MF | 2005 | Medicine (Baltimore)2005，84，2： | 1 |
| 4 | Post- source Decay Mass Spectrometry: Optimized Calibration Procedure and Structural Characterization of Pemrethylated Oligosaccharides显示文摘 | Viseux N Costrllo CE Domon B | 1999 | J Mass Spectrom1999，34，： | 1 |
| 5 | Brain magnetic resonance imaging in patients with Cowden syndrome显示文摘 | Lok C Viseux V Avril MF | 2005 | Medicine2005，84，2： | 1 |
| 6 | Pigmented purpuric dermatitis preceding the diagnosis of mycosis fungoides for 24 years显示文摘 | Viseux V Schoenlaub P Cnudde F | | 0，，03： | 1 |
| 7 | Topical silver sulfadiazine-induced acute renal failure 显示文摘 | CHABY G VISEUX V POULAIN J F | 2005 | Ann Dermatol Venereol2005，132，11： | 1 |
| 8 | Qualitative and quantitative analysis of the glycosylation pattern of recombinant proteins显示文摘 | Viseux N Hironowski X Delaney J | 2001 | Anal Chem2001，73，： | 1 |
| 9 | Multiple clustered dermatofibro- mas on a superficial venous thrombosis in a kidney-transplanted patient 显示文摘 | Viseux V Chaby G Agbalika F | 2004 | Dermatology2004，209，2： | 1 |
| 10 | 伊马替尼治疗后出现药物反应伴嗜酸性粒细胞增多症和系统症状(DRESS)(法语)显示文摘Background. Imatinib (GleevecTM) is a tyrosine kinase inhibitor used to treat chronic myeloid leukemia. We describe a case of drug reaction with eosinophilia and systemic symptoms (DRESS) after institution of treatment with imatinib. Patient and methods. A 78-year-old woman was treated with low-dose imatinib for chronic myeloid leukemia since November 2003. A macular and pruritic eruption appeared on the patient’s trunk after 7 weeks of treatment and gradually worsened. After 1 month, she was admitted for generalized skin eruption with fever and diffuse lymphadenopathy. Laboratory data showed hypereosinophilia and blood cultures positive for Staphylococcus aureus. Imatinib was stopped and replaced with hydroxyurea(HydreaTM). Improved clinical and laboratory results were seen with antibiotics and topical steroids. Discussion. To our knowledge, this is the first case of DRESS following treatment with imatinib. Cutaneous reactions to imatinib are frequent and are usually mild, comprising maculopapular eruption, pruritus and facial edema. Few cases of serious skin reactions have been reported until now. Several authors suggest that the prevalence and severity of cutaneous manifestations are related to a pharmacologic effect of imatinib. Our observation cannot rule out an underlying immunologic mechanism. Septicemia may also play a part in the development of DRESS. | Le Nouail P. Viseux V. Chaby G. 王琼 | 2006 | 世界核心医学期刊文摘(皮肤病学分册)2006，，12： | 0 |
| 11 | 黏液纤维肉瘤并发皮肤松弛(法语)显示文摘Background. Association of malignant cutaneous tumor and secondary anetoderma is rare. Secondary anetoderma in myxofibrosarcoma has not been described to date. We report a case below. Case report. A80-year-oldwoman presentedwith a 40 x 40 mm, round, flesh-colored lesion on her left buttock. Physical examination showed a soft, protuberant lesion, without firm underlying subcutaneous mass. Pathologic examination of the surgical specimen revealed a myxofibrosarcoma, with focal loss of elastic fibers in the overlying dermis. There was no evidence of systemic involvement. One year later, she developed a recurrent tumor at the same site, with similar clinical presentation, which was treated by broad excision. Discussion. Secondary anetoderma is usually seen in association with cutaneous infections and benign skin tumors. An anetodermic presentation of myxofibrosarcoma has not been reported to our knowledge. Myxofibrosarcoma (formerly referred to as myxoid malignant fibrous histiocytoma) is characterized by an abundant myxoid background in at least one half of the tumor. The tumor recurs in almost two-thirds of cases and metastasizes in one-fourth. Our case confirms that a unique, acquired anetodermic lesion can reveal a malignant tumor. A large deep biopsy should be performed systematically when this variety of anetoderma is observed. | Chaby G. Viseux V. Chatelain D. 焦婷 | 2006 | 世界核心医学期刊文摘(皮肤病学分册)2006，0，4： | 0 |
| 12 | 与肠道病毒血清转化有关的假血管瘤样发疹(法语) | Davaine A.-C. Viseux V. Staroz F. Plantin P. 刘超 | 2005 | 世界核心医学期刊文摘(皮肤病学分册)2005，0，4： | 0 |
| 13 | 治疗相关动-静脉瘘引发手部静脉性溃疡显示文摘Background. An arteriovenous fistula of the arm for hemodialysis needs to last long and provide easy access for puncture. Case-report. A 50 year-old woman, with type 2 diabetes complicated by chronic renal failure, presented with an ulcer on the dorsum of the right hand that had developed over the past year. Humeral artery to basilica vein, side-to-side, arteriovenous fistula in the right arm was created in 1996. In 1999, she received a renal transplant. In 2002, she developed a deep ulcer on the dorsum of the right hand that progressed over one year, without improvement good local treatment. Doppler echography and a fistulography revealed proximal stenosis of the basilica vein, and a less restricted distal stenosis before the shunt. A venous ulcer on the dorsum of the hand due excessive venous pressure in the draining area. Discussion. The complications of arteriovenous fistulas can be severe. Arterial stenosis is frequent and is the consequence of intimal hypertrophy. Chronic ischemia symptoms can be observed, but the hemodynamic loss is usually asymptomatic. When clinical signs are noisy emergency surgery is required. Venous stenosis is responsible for ischemia through venous overload, leading to edema of the arm, and rarely to venous-ulcer type trophic disorders as seen in this patient. Screening for stenosis on the vascular vein network must be systematic before creating an arteriovenous fistula. | Boulenger-Vazel A. Viseux V. Schoenlaub P. P. Plantin 周少娜 | 2006 | 世界核心医学期刊文摘(皮肤病学分册)2006，2，3： | 0 |
| 14 | 经毛囊穿破的穿通性环状肉芽肿(法国) | Billet A. Viseux V. Chaby G. 惠海英 | 2005 | 世界核心医学期刊文摘(皮肤病学分册)2005，0，12： | 0 |
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