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[Subcutaneous nodules and sensitivity to aluminum in patients undergoing hyposensitivity immunotherapy]. [低敏性免疫治疗患者皮下结节和对铝的敏感性]。
Q4 Medicine Pub Date : 1990-01-01
V García-Patos, A Alomar, R Lleonart, A Cistero, X Matias-Guiu

Hypersensitivity reactions to aluminium are very rate. Sensitization has been reported to occur during continuous application of aluminium-containing antiperspirants or by aluminium adjuvants in vaccines and hyposensitization immunotherapy. We report 5 patients who developed persistent and itching subcutaneous nodules following immunotherapy. Histologically, the nodules showed a granulomatous reaction consistent with delayed hypersensitivity to aluminium. Patch tests with 2% aluminium chloride in water were positive in three patients, and positive results of patch test with other metals (nickel, cobalt) were frequently associated.

对铝的过敏反应非常普遍。据报道,在持续使用含铝止汗剂或在疫苗和低敏免疫疗法中使用铝佐剂时,会发生致敏。我们报告了5例在免疫治疗后出现持续瘙痒的皮下结节的患者。组织学上,结节表现为肉芽肿反应,与铝的迟发性超敏反应一致。3名患者用2%氯化铝水溶液进行斑贴试验呈阳性,用其他金属(镍、钴)进行斑贴试验也经常出现阳性结果。
{"title":"[Subcutaneous nodules and sensitivity to aluminum in patients undergoing hyposensitivity immunotherapy].","authors":"V García-Patos,&nbsp;A Alomar,&nbsp;R Lleonart,&nbsp;A Cistero,&nbsp;X Matias-Guiu","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Hypersensitivity reactions to aluminium are very rate. Sensitization has been reported to occur during continuous application of aluminium-containing antiperspirants or by aluminium adjuvants in vaccines and hyposensitization immunotherapy. We report 5 patients who developed persistent and itching subcutaneous nodules following immunotherapy. Histologically, the nodules showed a granulomatous reaction consistent with delayed hypersensitivity to aluminium. Patch tests with 2% aluminium chloride in water were positive in three patients, and positive results of patch test with other metals (nickel, cobalt) were frequently associated.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 2","pages":"83-8"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13299108","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Mycosis fungoides associated with follicular mucinosis in an adolescent. Presentation of a case]. [1例青少年伴滤泡性黏液病的蕈样真菌病。提出一个案例]。
Q4 Medicine Pub Date : 1990-01-01
A L Bittencourt, N Ferras de Castro Dias, L Rocha Guimarães de Souza, W Affonso de Carvalho

The authors present a case of mycosis fungoides with an early onset, at the age of 15 years. It was manifested as hypopigmented lesions and was associated with follicular mucinosis. The invulgar aspects of this case let to erroneous diagnosis and possibilitate the evolution of disease to the tumoral phase. The patient presented a good response to therapy.

作者提出一个病例蕈样真菌病早发,在年龄15岁。表现为低色素病变,并伴有滤泡性黏液增多症。这个病例的不寻常之处会导致错误的诊断,并可能使疾病发展到肿瘤阶段。病人对治疗反应良好。
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引用次数: 0
[Angioimmunoblastic lymphadenopathy with dysproteinemia. The first reported case at the "Santo Tomás" Hospital]. 血管免疫母细胞淋巴结病伴蛋白异常血症。第一例报告病例发生在"Santo Tomás"医院]。
Q4 Medicine Pub Date : 1990-01-01
A A Ospino, R Ermocilla, H A Schlager, P E Ospino de Schlager, J V Pachar, R Da Silva, D Pereira

Description of the first case of angio-immunoblastic lymphadenopathy with dysproteinemia diagnosed in a male patient 64 years old and which preceded the development of a lymphoma. The importance of this study is the association that may exist between certain drugs and the development of angioimmunoblastic lymphadenopathy, which occurred in our patient with the use of diphenylhydantoin. This disease can present itself up to 22 years after exposure to the agent.

第一例血管免疫母细胞性淋巴结病伴蛋白异常血症,诊断于64岁男性患者,并先于淋巴瘤的发展。本研究的重要性在于某些药物与血管免疫母细胞性淋巴结病的发展之间可能存在关联,我们的患者使用了二苯基苯妥英。这种疾病可在接触病原体22年后出现。
{"title":"[Angioimmunoblastic lymphadenopathy with dysproteinemia. The first reported case at the \"Santo Tomás\" Hospital].","authors":"A A Ospino,&nbsp;R Ermocilla,&nbsp;H A Schlager,&nbsp;P E Ospino de Schlager,&nbsp;J V Pachar,&nbsp;R Da Silva,&nbsp;D Pereira","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Description of the first case of angio-immunoblastic lymphadenopathy with dysproteinemia diagnosed in a male patient 64 years old and which preceded the development of a lymphoma. The importance of this study is the association that may exist between certain drugs and the development of angioimmunoblastic lymphadenopathy, which occurred in our patient with the use of diphenylhydantoin. This disease can present itself up to 22 years after exposure to the agent.</p>","PeriodicalId":18373,"journal":{"name":"Medicina cutanea ibero-latino-americana","volume":"18 1","pages":"1-4"},"PeriodicalIF":0.0,"publicationDate":"1990-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"13366268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Cutaneo-visceral leishmaniasis: a new opportunistic infection in patients infected by HIV]. 皮肤-内脏利什曼病:HIV感染患者的一种新的机会性感染。
Q4 Medicine Pub Date : 1990-01-01
R Botella Estrada, O Sanmartín Jiménez, M I Febrer Bosch, A Aliaga Boniche, M Salavert Lleti, P Roig Rico, A Nieto García, V Navarro Ibañez

A HIV infected patient was admitted to hospital with fever diarrhoea and a cutaneous nodule on his left groin. Histopathological exam was diagnostic of cutaneous leishmaniasis. Subsequent exams disclosed Visceral Leishmaniasis. Three cycles of treatment (antimonials, pentamidine and metronidazole) were required for the clearance of lesions. The relation between immunosuppression and leishmania infection is commented and its role as an opportunistic pathogen is suggested. In these patients the infection takes a more aggressive course and has a worse response to the classic treatment with antimonials. These facts have made necessary the introduction of other alternative drugs.

一名感染艾滋病毒的病人因发烧、腹泻和左腹股沟皮肤结节入院。组织病理学检查诊断为皮肤利什曼病。随后的检查发现内脏利什曼病。三个周期的治疗(锑、喷他脒和甲硝唑)需要清除病变。本文评述了免疫抑制与利什曼原虫感染的关系,并提出了利什曼原虫作为条件致病菌的作用。在这些患者中,感染的过程更具侵略性,对抗疟药的经典治疗反应更差。这些事实使得引入其他替代药物成为必要。
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引用次数: 0
[Sea-blue histiocytes in a patient with mycosis fungoides]. [蕈样真菌病患者的海蓝色组织细胞]。
Q4 Medicine Pub Date : 1990-01-01
F Allegue, C Soria, L Escribano, A Rocamora, R Moreno, A Ledo

The syndrome of the sea-blue histiocyte is a multisystemic infiltration by a special kind of macrophages which contain a ceroid material within its cytoplasm. We report herein a patient with mycosis fungoides, hyperlipidaemia type IIB and sea-blue histiocytes on bone marrow. Moreover, the cutaneous histopathology showed focus of eosinophilic spongiosis, that have not been previously described in mycosis fungoides, as far as we know.

海蓝组织细胞综合征是一种特殊的巨噬细胞的多系统浸润,其细胞质内含有类胶质物质。我们在此报告一例伴有蕈样真菌病、高脂血症IIB和骨髓海蓝色组织细胞的患者。此外,据我们所知,皮肤组织病理学显示嗜酸性海绵状病的焦点,这在真菌样真菌病中尚未被描述。
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引用次数: 0
[Dowling-Degos disease]. (Dowling-Degos疾病)。
Q4 Medicine Pub Date : 1990-01-01
V Fernández-Redondo, A Losada, A Zulaica, C Cebreiro, R Cervantes, J Toribio

We report two cases of Dowling-Degos' disease, one affecting the vulvovaginal semimucose, and one associated to a terminal malignant neoplasia. We remark the importance of this knowledge in order to distinguish it from malignant acanthosis nigricans or other patterns of melanosis or lentiginosis when located within mucose or semimucose, specially at the genitals. All cases associated to malignant neoplasia described are emphasized. However Dowling-Degos' disease is considered to be a nonparaneoplasic genodermatoses, this association should be taken into account.

我们报告两例Dowling-Degos病,一个影响外阴阴道半粘液,一个与终末期恶性肿瘤相关。我们注意到这种知识的重要性,以便将其与恶性黑皮病或其他类型的黑素病或小痣病区分开来,当位于粘膜或半粘膜内时,特别是在生殖器。强调所有与恶性肿瘤相关的病例。然而,Dowling-Degos病被认为是一种非副肿瘤性遗传性皮肤病,应考虑到这种关联。
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引用次数: 0
[Cystic lymphangioma]. 囊性淋巴管瘤。
Q4 Medicine Pub Date : 1990-01-01
J C Moreno Giménez, F Camacho, J J Ríos Martín, J R Armas Padrón

A case of clinical and dermopathological characteristic cystic lymphangioma is reported. The atypical localization of the tumor and its delayed apparition were pointed out. A relation with any precipitating factor could not be established. Treatment was surgical remove.

本文报告1例具有临床及皮肤病理特征的囊性淋巴管瘤。指出肿瘤的不典型定位和延迟出现。不能确定与任何促成因素的关系。治疗方法为手术切除。
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引用次数: 0
[Acute neutrophilic febrile dermatosis (Sweet syndrome) associated with melanoma]. [与黑色素瘤相关的急性中性粒细胞发热性皮肤病(Sweet综合征)]。
Q4 Medicine Pub Date : 1990-01-01
J Sánchez Conejo-Mir, A Perez Bernal, F Camacho

A 45-years-old woman affected of Acute febrile neutrophilic syndrome is presented, with no reliable etiology. In a rutinary control, a pigmented ledion of one year of evolution was observed and a surgical excision was performed, with histological diagnosis of spreading superficial melanoma. In the next weeks of post-operatory, the Sweet's syndrome was decreased, disappearing completely two months later. No recurrences of Sweet's syndrome or malignant melanoma were observed after two years of follow-up. Association between Sweet's syndrome and neoplasias, in particular solid tumors, is commented, and the literature is reviewed.

一个45岁的妇女感染急性发热中性粒细胞综合征,没有可靠的病因。在常规对照中,观察到一年进化的色素斑点,并进行手术切除,组织学诊断为弥漫性浅表黑色素瘤。在术后的几周内,斯威特氏综合症有所减轻,两个月后完全消失。随访2年后,未发现Sweet综合征或恶性黑色素瘤复发。Sweet’s综合征与肿瘤,特别是实体瘤之间的关系,被评论,并回顾了文献。
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引用次数: 0
[Topical Vitamin E and ultraviolet radiation on human skin]. [局部维生素E和人体皮肤上的紫外线辐射]。
Q4 Medicine Pub Date : 1990-01-01
R Rampoldi, N Macedo, W Alallon, J Sanguimetti

The point is the relation between the tissue damage caused by UV radiations, the production of free radicals (lipoperoxidation) and the particular action of vitamin E on human skin. Through histopathologic changes and malondialdehyde dosification results, are analyzed, therefore a close relation between UV radiation, free radicals, lipoperoxidation, and tissue damage, is proved on human skin. Furthermore the protective action of topic vitamin E antioxidant which diminishes the lipoperoxidation and the tissue damage is apparent.

重点是紫外线辐射引起的组织损伤、自由基的产生(脂质过氧化)和维生素E对人体皮肤的特殊作用之间的关系。通过对组织病理学变化和丙二醛剂量化结果的分析,从而证明了紫外线辐射、自由基、脂质过氧化和人体皮肤组织损伤之间的密切关系。此外,主题维生素E抗氧化剂具有明显的保护作用,可减轻脂质过氧化和组织损伤。
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引用次数: 0
[Leukocyte phagocytic activity in gerbils with experimental sporotrichosis treated with potassium iodide]. [用碘化钾治疗实验性孢子虫病沙鼠白细胞吞噬活性]。
Q4 Medicine Pub Date : 1990-01-01
R Ramos Zepeda, R Ramos Zepeda, M E Ramos Damian, B M González Rico, A González Mendoza

One effective treatment against sporotrichosis is the oral administration of potassium iodide (KI). It is not known how it works, and also it is not known if this substance has some effect on the microbicidal activity of polymorphonuclear neutrophils (PMN) and macrophages. In this work the phagocytic activity of gerbils treated with KI was studied. Gerbils cured within 62 days of treatment with KI, their PMN and macrophages showed an increased ability for reducing nitroblue-tetrazolium (NBT); myeloperoxidase activity was decreased in PMN. These results were the expected in any chronic infection and demonstrates that KI effectiveness on the experimental sporotrichosis works by an independent mechanism of phagocytosis.

一种有效的治疗孢子虫病是口服碘化钾(KI)。目前尚不清楚它是如何起作用的,也不清楚这种物质是否对多形核中性粒细胞(PMN)和巨噬细胞的杀微生物活性有一定影响。本文研究了经KI处理的沙鼠的吞噬活性。经KI治疗62天内治愈的沙鼠,其PMN和巨噬细胞还原硝基蓝-四氮唑(NBT)的能力增强;髓过氧化物酶活性在PMN中降低。这些结果在任何慢性感染中都是预期的,并表明KI对实验性孢子虫病的有效性是通过独立的吞噬机制起作用的。
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引用次数: 0
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Medicina cutanea ibero-latino-americana
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