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Clinically relevant differences between amelanotic malignant melanoma and granuloma pyogenicum. 无色素性恶性黑色素瘤与化脓性肉芽肿的临床差异。
Pub Date : 1991-01-01 DOI: 10.1159/000247750
I D Bassukas, A Kuhnert, T L Diepgen, O P Hornstein

Macroscopic discrimination between amelanotic malignant melanoma (aMM) and the so-called granuloma pyogenicum (GP) is often uncertain since reliable criteria for a clear differentiation of either growth are lacking. In a search of such criteria we analysed the data of 57 consecutive in-patients with cutaneous aMM and of 83 with GP presenting at our Department during the years 1970-1988. The following items were compared with each other: duration from growth onset to definite diagnosis, site of growth, age and sex of the patients. Significant differences (p less than 0.01) between either growth were found for all items evaluated. Our results substantiate the hitherto gained impression of a remarkably shorter median history of GP as compared to aMM (5 vs. 26 weeks). Furthermore, aMM prevailed in elder (age greater than 50 years) particularly female (70%) patients, whereas GP developed about equally in both sexes and at all ages. Site distribution was also found to differ for either growth (GP predominantly in the head and neck region, rarely on lower limbs; aMM in all areas, rarely on the trunk). These data yield additional measures for clinical distinction between aMM and GP.

无色素瘤恶性黑色素瘤(aMM)和所谓的化脓性肉芽肿(GP)的肉眼鉴别通常是不确定的,因为缺乏明确区分这两种生长的可靠标准。为了寻找这样的标准,我们分析了1970-1988年间在我科连续就诊的57例皮肤性aMM住院患者和83例全科医生的数据。比较以下项目:从生长开始到确诊的时间、生长部位、患者年龄和性别。在所有评估项目中,两种生长之间存在显著差异(p < 0.01)。我们的结果证实了迄今为止获得的印象,即与aMM相比,GP的中位病史明显更短(5周对26周)。此外,aMM主要见于老年人(50岁以上),尤其是女性(70%),而GP在两性和所有年龄段的发病率大致相同。两种生长的部位分布也不同(GP主要发生在头颈部,很少发生在下肢;aMM在所有区域,很少在主干)。这些数据为aMM和GP之间的临床区别提供了额外的措施。
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引用次数: 4
Pseudohomozygous type II hyperlipoproteinemia. 假纯合型II型高脂蛋白血症。
Pub Date : 1991-01-01 DOI: 10.1159/000247753
M Fujita, S Okamoto, K Shirai, Y Saito, S Yoshida

Nodular xanthomas on both elbows and a streak-like xanthoma on the intergluteal area developed in a 4-year-old girl with type IIa hyperlipoproteinemia. She had no disease associated with secondary hypercholesterolemia and no family history of hypercholesterolemia. Her xanthomas regressed under fat restriction diet and cholestyramine therapy. She was diagnosed as having pseudohomozygous type II hyperlipoproteinemia. The low-density lipoprotein (LDL) receptor activities of her cultured fibroblasts in terms of binding, internalization and degradation rate of LDL were normal. These results are consistent with a new syndrome of pseudohomozygous type II hyperlipoproteinemia and suggest that the mechanism of hypercholesterolemia, which induced xanthoma, differs from familial hypercholesterolemia.

一例4岁女孩患IIa型高脂蛋白血症,双肘结节状黄瘤和臀间区条状黄瘤。患者无继发性高胆固醇血症相关疾病,无高胆固醇血症家族史。在脂肪限制饮食和胆胺治疗下,她的黄瘤消退。她被诊断为假纯合型II型高脂蛋白血症。其培养成纤维细胞的低密度脂蛋白(LDL)受体活性在LDL的结合、内化和降解率方面均正常。这些结果与伪纯合子型II型高脂蛋白血症的新综合征一致,并提示高胆固醇血症诱发黄瘤的机制不同于家族性高胆固醇血症。
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引用次数: 7
Treatment of inflammatory linear verrucous epidermal nevus. 炎性线状疣状表皮痣的治疗。
Pub Date : 1991-01-01 DOI: 10.1159/000247756
H F Rulo, P C van de Kerkhof

Inflammatory linear verrucous epidermal nevus (ILVEN) is a rare and chronic skin disorder, which may trouble the patient considerably. The condition is generally believed to be resistant to therapy, although some authors have reported success with several treatments. including dithranol and etretinate. The present case, a classical presentation of ILVEN, again illustrates the refractoriness to various treatments, including an experimental treatment with topical 13-cis-retinoic acid. A review of the literature on therapeutic possibilities of ILVEN is presented. Based on our own observations and literature data, it is attractive to hypothesize that a positive result with treatments such as dithranol and retinoids should be interpreted as an antipsoriatic effect in ILVEN with superimposed psoriasis.

炎性线状疣状表皮痣(ILVEN)是一种罕见的慢性皮肤病,可能会给患者带来很大的困扰。这种情况通常被认为对治疗有抵抗力,尽管一些作者已经报道了几种治疗方法的成功。包括双糖醇和醋酸酯。本病例是典型的ILVEN,再次说明了各种治疗的难治性,包括局部使用13-顺式维甲酸的实验性治疗。本文综述了有关ILVEN治疗可能性的文献。根据我们自己的观察和文献资料,我们有兴趣假设,在合并银屑病的ILVEN中,双糖醇和类维生素a治疗的阳性结果应该被解释为抗银屑病的效果。
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引用次数: 26
Kaposi's sarcoma + HIV infection = AIDS? 卡波西肉瘤+ HIV感染=艾滋病?
Pub Date : 1991-01-01 DOI: 10.1159/000247743
M Harms, S Kinloch, J H Saurat
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引用次数: 0
Dermatomyositis and pregnancy. Case report and review of the literature. 皮肌炎与妊娠。病例报告及文献复习。
Pub Date : 1991-01-01
N Ishii, H Ono, T Kawaguchi, H Nakajima

Dermatomyositis is a rare disease complicating pregnancy. We treated a patient in whom two pregnancies were complicated by dermatomyositis. In the first of the two gestations, a mild form of the disease arose in the last trimester. In the second gestation, the disease was inactive following treatment with 0.3 mg/kg/day prednisolone. Both the mother and two children have since been doing well.

皮肌炎是一种罕见的妊娠并发症。我们治疗了一位两次妊娠合并皮肌炎的患者。在两次妊娠的第一次中,在最后三个月出现了轻度的疾病。在第二次妊娠中,用0.3 mg/kg/天的强的松龙治疗后,疾病无活性。从那以后,母亲和两个孩子都恢复得很好。
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引用次数: 0
Intermittent corticosteroid maintenance treatment of psoriasis: a double-blind multicenter trial of augmented betamethasone dipropionate ointment in a pulse dose treatment regimen. 间歇皮质类固醇维持治疗银屑病:脉冲剂量治疗方案中增强倍他米松软膏的双盲多中心试验
Pub Date : 1991-01-01 DOI: 10.1159/000247698
H I Katz, S E Prawer, R S Medansky, G G Krueger, J J Mooney, M L Jones, C R Samson

Ninety psoriasis patients, who were either completely cleared of or manifested only a minimal presence of disease signs following 3-4 weeks of twice daily treatment with augmented betamethasone dipropionate (ABD) ointment 0.05%, were enrolled in this multicenter, double-blind, placebo-controlled study. The study was designed to determine if an intermittent pulse dose regimen of ABD ointment could safely and effectively maintain a remission disease status when treatment was applied in three consecutive applications 12 h apart, once a week for a maximum treatment period of 6 months. The disease of 60% of the patients in the active treatment group was successfully controlled for 6 months, while 80% of the placebo-treated patients experienced exacerbation of disease signs. No serious local or systemic treatment-related adverse experiences were reported. ABD ointment 0.05%, when applied using the intermittent treatment regimen described here, was shown to be a clinically beneficial and well-tolerated method of long-term (up to 6 months) maintenance therapy for psoriasis patients.

90名牛皮癣患者,在0.05%的增强倍他米松二丙酸软膏治疗3-4周后,要么完全清除,要么仅表现出最小的疾病体征,纳入了这项多中心、双盲、安慰剂对照研究。该研究旨在确定ABD软膏的间歇脉冲剂量方案是否可以安全有效地维持疾病缓解状态,当治疗连续三次,每次间隔12小时,每周一次,最长治疗期为6个月。积极治疗组60%的患者病情得到成功控制6个月,而安慰剂治疗组80%的患者出现疾病体征加重。没有严重的局部或全身治疗相关的不良经历报告。0.05% ABD软膏,当使用本文描述的间歇治疗方案时,被证明是临床有益且耐受性良好的长期(长达6个月)维持治疗银屑病患者的方法。
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引用次数: 68
Cutaneous metastases from follicular thyroid carcinoma: histology, immunohistology, and electron microscopy. A report of two cases. 甲状腺滤泡癌皮肤转移:组织学、免疫组织学和电镜。报告两个病例。
Pub Date : 1991-01-01 DOI: 10.1159/000247702
M Tronnier, M Winzer, H H Wolff

Cutaneous metastases from thyroid carcinoma are extremely rare. We report 2 cases of skin metastases from a follicular thyroid carcinoma. A 53-year-old female patient underwent subtotal thyroidectomy because of the clinical suspicion of malignancy. Histological examination of the resected tissue did not clearly prove malignant features. Eight years later a cutaneous metastasis erupted next to the operation site at the neck. A 66-year-old female patient noticed a growing solitary skin nodule in the occipitoparietal region of her scalp 2 years before a follicular thyroid carcinoma was detected.

甲状腺癌的皮肤转移极为罕见。我们报告2例皮肤转移的滤泡性甲状腺癌。一位53岁女性患者因临床怀疑为恶性肿瘤而行甲状腺次全切除术。切除组织的组织学检查未明确证实恶性特征。八年后,颈部手术部位附近出现皮肤转移。一位66岁的女性患者在发现滤泡性甲状腺癌2年前,发现头皮枕顶区有一个孤立的皮肤结节。
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引用次数: 21
Decreased isotretinoin efficacy during acute alcohol intake. 急性酒精摄入期间异维a酸疗效降低。
Pub Date : 1991-01-01 DOI: 10.1159/000247785
C Soria, F Allegue, J Galiana, A Ledo
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引用次数: 13
Darier's disease and corneal opacity. 达里尔病与角膜混浊。
Pub Date : 1991-01-01 DOI: 10.1159/000247787
K N Mohamed
.Tear film – Surface cells -Wing cells Epithelium-■Basement 7 Bowman’s layer The cornea and conjunctiva can be considered as modified skin ‚ and cutaneous disorders, especially that involving the epidermis, also affect the corneal epithelium. The epithelium, derived from the surface ectoderm is a 5to 6-cell layer forming 10% of the corneal thickness; the stroma which is of mesodermal origin forms about 90% [1]. The basal cells that are attached to the basement membrane by hemidesmosomes give rise to wing cells which become the surface cells and are shed into the tears (fig. 1); thus, the corneal epithelium is structurally and physiologically somewhat similar to the epidermis. A case of Darier’s disease with a peripheral corneal opacity is reported to stress the importance of examining the eyes in this genodermatosis. A 36-year-old Malay lady was referred to the Skin Clinic for a spreading papular, warty lesion on the body since childhood. She was treated in the Eye Ward for a small left corneal ulcer of undetermined cause. The patient was a gravida 8, para 7, in 34 weeks of gestation with no history of injury or foreign body in the eye. She presented with redness, pain, lacrimation and photophobia of the affected eye which on slit-lamp examination showed fluorescein staining of the cornea at the 6-o’clock position and few cells at the anterior chamber. She was treated with mydriatics and antibiotics, and after a week‚ the ulcer healed leaving an oval opacity. A skin biopsy confirmed Darier’s disease; her second son was also affected. We decided to start her on etretinate after a post-partum bilateral tubal ligation. There are several skin disorders, especially genodermatoses, which are associated with corneal changes. In a study involving 21 patients with Darier’s disease, various ocular abnormalities were observed [2]; unique peripheral corneal opacities, central corneal surface irregularities and keratotic plaques on eyelids were seen in 16 patients. The opacities were teardrop-sized to tiny, clustered oval-shaped lesions, and the irregularities were distributed in a radiating cobweb pattern. In two patients trephine biopsy of the opacities showed epithelial oedema especially of the basal cells and thickened basement membrane – features that are different from the skin pathology because the cornea is not a keratinizing epithelium. Darier’s disease in two brothers associated with retinitis pigmentosa has also been reported [3]. In view of the high prevalence of
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引用次数: 4
Verrucous carcinoma of a leg amputation stump. 腿部截肢残端疣状癌。
Pub Date : 1991-01-01 DOI: 10.1159/000247782
R A Schwartz, M P Bagley, C K Janniger, W C Lambert

Verrucous carcinoma of the skin is a rare cancer which tends to appear on the soles of the feet, although it can appear elsewhere on the cutaneous surface. It has not, to our knowledge, been previously reported on a leg amputation stump.

皮肤疣状癌是一种罕见的癌症,往往出现在脚底,尽管它可以出现在皮肤表面的其他地方。据我们所知,以前没有在截肢残肢上报道过。
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引用次数: 25
期刊
Dermatologica
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