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Focal acantholytic dyskeratosis: a snare for the pathologist. Report of two cases associated to psoriasis and fibrous papule of the nose. 局灶性棘溶性角化不良:病理学家的陷阱。牛皮癣合并鼻纤维丘疹2例报告。
Pub Date : 1992-09-01
M L Cintra, E M de Souza

Two specimens containing clinically inapparent histologic features of acantholytic dyskeratosis (on the base of a fibrous papule of the nose and overlying a psoriatic lesion) are presented. The authors discuss the conduct to be followed by the pathologist in similar cases. The general pathologist should be well trained in dermatopathology since cutaneous biopsies account for 10 to 25% of the specimens submitted for histologic diagnosis or, even, form the major part of the workload (Berry). There is a wall between the physician who submits the skin biopsies (who may be or not a dermatologist) and the pathologist. The clinical information provided by dermatologists is scant and incomplete and physicians who are not dermatologists seldom submit any information. The histological pictures found in skin biopsies are, often, common to several nosological entities and an adequate understanding of their meaning is desirable for a thorough evaluation. We ought to assess it with the maximum scientific severity, searching to solve the puzzle without depreciating the information received. In this report the authors analyse the histopathological approach to the cutaneous lesions of two patients. They displayed the association between acantholytic dyskeratosis (AD) and another cutaneous pathology. Findings like these may obstruct the final diagnosis to be issued by the pathologist.(ABSTRACT TRUNCATED AT 250 WORDS)

两个标本包含临床不明显的棘溶解性角化不良的组织学特征(位于鼻子纤维丘疹的底部和银屑病病变的上方)。作者讨论了病理学家在类似病例中应遵循的行为。一般病理学家应该在皮肤病理学方面受过良好的培训,因为皮肤活检占提交的组织学诊断标本的10%到25%,甚至是工作量的主要部分(Berry)。提交皮肤活检报告的医生(可能是皮肤科医生,也可能不是皮肤科医生)和病理学家之间有一堵墙。皮肤科医生提供的临床信息是缺乏和不完整的,医生谁不是皮肤科医生很少提交任何信息。在皮肤活组织检查中发现的组织学图片通常是几种疾病实体的共同特征,对其含义的充分理解对于彻底的评估是可取的。我们应该用最科学的严肃性来评估它,在不贬低所收到的信息的情况下,努力解决这个难题。在本报告中,作者分析了两例皮肤病变的组织病理学方法。他们显示棘溶解性角化不良症(AD)和另一种皮肤病理之间的联系。这样的发现可能会阻碍病理学家做出最终诊断。(摘要删节250字)
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引用次数: 0
ISBT Brazil '92. XXII Congress of the International Society of Blood Transfusion. XX Brazilian Congress of Hematology. Extraordinary Congress of the Brazilian College of Hematology. Sao Paulo, Brazil. October 8-13, 1992. Abstracts. 1992年巴西ISBT。第22届国际输血学会大会。第20届巴西血液学大会。巴西血液学院特别代表大会。巴西圣保罗。1992年10月8日至13日。摘要。
Pub Date : 1992-09-01
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引用次数: 0
Mediastinitis after cervical suppuration. 宫颈化脓后的纵隔炎。
Pub Date : 1992-09-01
A S Esgaib, M C Ghefter, R de M Lyra, R B Guidugli, A L Trajano, S M Ferreira

The objective of this study is to decode the etiopathogenesis, the clinical feature, the diagnosis and the prognosis of the acute mediastinitis resulting of infectious processes of the cephalic segment. Three out of five patients studied presented focus of dental origin and two patients presented focus in the face area. One of them presented Ludwig's Angina before the suppurative process would spread over the mediastinum. In the others, there was fast expansion through the fascial spaces of the neck and, in two of them, besides the mediastinum, there was pleuropericardial involvement. Three patients died due to respiratory insufficiency and two survived with complications. The mediastinitis after cervical suppuration is a special and extremely serious kind of endothoracic infection. The pus reaches that area through the fascial spaces of the neck, taking the organism to an alarming toxemic feature. The rarity of the disease, the little is known about its physiopathology and the initial care of the patient in non-specialized services, which are not familiarized with this type of feature, are factors that can delay the diagnosis and worsen the prognosis.

本研究旨在探讨头节感染性过程引起的急性纵隔炎的发病机制、临床特点、诊断及预后。5例患者中有3例出现牙源性病灶,2例出现面部病灶。其中一人在化脓性过程扩散到纵隔之前出现了路德维希心绞痛。在其他病例中,颈部筋膜间隙迅速扩张,其中两例,除纵隔外,还累及胸膜心包。3名患者因呼吸功能不全死亡,2名患者因并发症存活。宫颈化脓后纵隔炎是一种特殊而又极为严重的胸廓内感染。脓液通过颈部的筋膜间隙到达该区域,使生物体具有令人担忧的毒血症特征。这种疾病的罕见性,对其生理病理知之甚少,以及在不熟悉这种特征的非专业服务部门对患者的初始护理,都是可能延迟诊断和恶化预后的因素。
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引用次数: 0
A critical appraisal of the value of vaginal acid phosphatase determination for the estimation of post-coital time. 阴道酸性磷酸酶测定对估计性交后时间的价值的关键评价。
Pub Date : 1992-07-01
A R Meira, J A Soares-Vieira, J M Souza

A careful literature review of the use of vaginal fluid acid phosphatase levels as a means to estimate post-coital time disclosed several inconsistencies. In this study, acid phosphatase levels were determined in vaginal fluid samples obtained from 200 women whose post-coital time was known. No statistical significance (at 5% probability levels) was found when vaginal acid phosphatase levels were correlated with post-coital time.

对使用阴道液酸性磷酸酶水平作为估计性交后时间的手段进行了仔细的文献审查,发现了几个不一致之处。在这项研究中,测定了200名已知性交后时间的女性阴道液样本中的酸性磷酸酶水平。阴道酸性磷酸酶水平与性交后时间的相关性无统计学意义(在5%的概率水平下)。
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引用次数: 0
Primary lymphoma of the breast. 乳腺原发性淋巴瘤。
Pub Date : 1992-07-01
A C Nazário, C I Tanaka, G R de Lima, L H Gebrim, V Chiferi Júnior

We describe a case of primary lymphoma of the breast which clinically mimicked a phyllodes tumor. The diagnosis and treatment of this rare neoplasm are discussed. The lymphomas, neoplasias of the immune system, comprise a large group of proliferative diseases of the lymphoreticular tissue which are classified into two histological types, i.e., Hodgkin and non-Hodgkin. Primary lymphomas of the breast are quite rare, with an incidence ranging from 0.4 to 0.53% of all malignant breast tumors (2). They are characterized by uni- or bilateral involvement of the breast, with or without homolateral axillary lymphadenopathy, and by the absence of lymphatic disease at another site (7). We report here a case of primary non-Hodgkin lymphoma of the left breast and we discuss its clinical aspects and the treatment instituted.

我们报告一例原发性乳腺淋巴瘤,临床表现酷似叶状瘤。本文讨论了这种罕见肿瘤的诊断和治疗。淋巴瘤,免疫系统的肿瘤,包括一大类淋巴网状组织的增生性疾病,分为两种组织学类型,即霍奇金和非霍奇金。乳腺原发性淋巴瘤非常罕见,在所有乳腺恶性肿瘤中的发病率为0.4 - 0.53%(2)。其特征为单侧或双侧累及乳房,伴或不伴同侧腋窝淋巴结病,且在其他部位无淋巴疾病(7)。我们在此报告一例左乳原发性非霍奇金淋巴瘤,并讨论其临床特点和治疗方法。
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引用次数: 0
Deflection of T tube in the choledochus, simulating retained stone. 胆道内T管偏转,模拟结石残留。
Pub Date : 1992-07-01
J M Netto, M B Speranzini
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引用次数: 0
Sydenham chorea: clinical and laboratory findings. Analysis of 187 cases. 西德纳姆舞蹈病:临床和实验室结果。187例分析。
Pub Date : 1992-07-01
J Goldenberg, M B Ferraz, A S Fonseca, M O Hilário, W Bastos, S Sachetti

Sydenham's chorea (chorea minor, St. Vitus dance, rheumatic encephalitis), described by Thomas Sydenham in 1686, is considered one of the major manifestations of rheumatic fever (1, 2, 3, 4). Clinically it is characterized by involuntary movements, hypotonia, dysarthria, emotional disorders, and less frequently, by other neurological manifestations such as weakness, headache, seizures and sensory abnormalities (1,4). The motor disorders may be generalized or unilateral, in this case constituting a hemichorea (3). Chorea may present associated to other rheumatic fever manifestations during an acute episode, or in isolated form, characterizing the so-called "pure" chorea (5, 6, 7). Its etiology and pathophysiological mechanisms are still unclear, although its relation with a previous pathophysiological group A Beta-hemolytic streptococcus infection is well established (8). There is also evidence of the participation of immunological mechanisms in its pathogenesis, such as the finding of serum anti-nucleus caudatus and anti-subthalamic antibodies (9) and increase in IgG levels in cerebrospinal fluid of patients with chorea (10). In developed countries due to the reduction in rheumatic fever incidence and decrease in frequency of chorea as its manifestation (3, 11), the latter has become rare. However, in developing countries rheumatic fever remains a public health problem. In Brazil, in the last years an increase in the incidence of chorea has been observed as part of the clinical picture of rheumatic fever (12). The present study reports the clinical and laboratory findings of 187 cases of Sydenham's chorea followed-up during the period of January 1980 to December 1990 in two university centers in the city of Sao Paulo, Brazil.

1686年,托马斯·西德纳姆(Thomas Sydenham)描述了西德纳姆舞蹈病(小舞蹈病、圣·维图斯舞蹈病、风湿性脑炎),被认为是风湿热的主要表现之一(1,2,3,4)。临床表现为不自主运动、强张、构音障碍、情绪障碍,其他神经系统表现如虚弱、头痛、癫痫发作和感觉异常等较少出现(1,4)。运动障碍可能是全身性的或单侧的,在这种情况下构成局部舞蹈病(3)。在急性发作期间,舞蹈病可能与其他风湿热表现相关,或以孤立形式出现,即所谓的“纯”舞蹈病(5,6,7)。其病因和病理生理机制尚不清楚。虽然它与先前的a组-溶血性链球菌感染的病理生理关系已经得到证实(8)。也有证据表明免疫机制参与了其发病机制,如发现血清抗尾状核和抗丘脑底抗体(9),以及舞蹈病患者脑脊液中IgG水平升高(10)。在发达国家,由于风湿热发病率的减少和以舞蹈病为表现的频率的减少(3,11),后者已变得罕见。然而,在发展中国家,风湿热仍然是一个公共卫生问题。在巴西,在过去几年中,作为风湿热临床表现的一部分,已经观察到舞蹈病发病率的增加(12)。本研究报告了1980年1月至1990年12月在巴西圣保罗市的两所大学中心随访的187例西德纳姆舞蹈病的临床和实验室结果。
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引用次数: 0
Generalized smooth muscle hypertrophy. 全身平滑肌肥大。
Pub Date : 1992-07-01
A L da Silva, A Petroianu

This report presents a twenty-year-old man with generalized digestive and urinary smooth muscle hypertrophy combined with somatic and sexual hypodevelopment. We could not find in the literature any report related to the disease of our patient. Congenital pyloric stenosis is the less rare obstructive syndrome due to smooth muscle hypertrophy. Morgagni described this syndrome in an adult patient, in the XVIII century (2). Pyloroplasty is the best treatment for this disease. Other congenital or acquired obstructive syndromes of the digestive system such as Chagas' aganglionosis and pseudo-obstruction of the small bowel are also important clinical and surgical challenges (1,3,4). Several obstructive illnesses due to smooth muscle dysfunction have been described. This report presents an apparently original syndrome urinary segmental obstruction following smooth muscle hypertrophy.

本报告报告一位二十岁男性,患有广泛性消化和泌尿平滑肌肥大,并伴有躯体和性发育不全。我们在文献中找不到任何与患者疾病相关的报道。先天性幽门狭窄是由于平滑肌肥大引起的较少见的梗阻性综合征。Morgagni在18世纪描述了一名成年患者的这种综合征(2)。幽门成形术是治疗这种疾病的最佳方法。其他先天性或获得性消化系统梗阻性综合征,如恰加斯神经节病和假性小肠梗阻,也是重要的临床和手术挑战(1,3,4)。一些由于平滑肌功能障碍引起的阻塞性疾病已经被描述过。本文报告了平滑肌肥厚引起的泌尿段梗阻。
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引用次数: 0
Perinatal factors associated with neural tube defects (anencephaly [correction of anancephaly], spina bifida and encephalocele). 与神经管缺陷(无脑畸形、脊柱裂和脑膨出)相关的围产期因素。
Pub Date : 1992-07-01
A J Ogata, L Camano, D Brunoni

The objective of the present study was to determine the presence of risk factors for the occurrence of neural tube defects. Data for 33,535 births which occurred at Hospital do Servidor Público Estadual de São Paulo from July 1973 to December 1986 were collected in a prospective manner as recommended by "Estudo Colaborativo Latino-Americano de Malformações Congênitas" (ECLAMC, Collaborative Latin American Study on Congenital Malformations). Twenty-six cases of neural tube defects were detected (0.77/1000 births). Of these, 11 were cases of spina bifida (0.39/1000 births), 9 of anencephaly (0.27/1000 births) and 6 of encephalocele (0.18/1000 births). We observed a higher frequency of polyhydramnios, premature labor, Apgar scores of less than 7 at the first and fifth minutes, low birth weight and intrauterine growth retardation.

本研究的目的是确定神经管缺损发生的危险因素的存在。根据“Estudo colativo Latin - americano de Malformações Congênitas”(ECLAMC,拉丁美洲先天性畸形合作研究)的建议,以前瞻性的方式收集了1973年7月至1986年12月期间在Servidor Público Estadual de ss o Paulo医院出生的33,535例新生儿的数据。发现神经管缺陷26例(0.77/1000)。其中,脊柱裂11例(0.39/1000),无脑畸形9例(0.27/1000),脑膨出6例(0.18/1000)。我们观察到羊水过多、早产、第1分钟和第5分钟Apgar评分低于7分、低出生体重和宫内发育迟缓的发生率较高。
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引用次数: 0
Detection of estrogen receptor in formalin-fixed and paraffin-embedded breast carcinoma: correlation with histological patterns. 福尔马林固定和石蜡包埋乳腺癌中雌激素受体的检测:与组织学模式的相关性。
Pub Date : 1992-07-01
F C Schmitt, L M Andrade, L A de Lucca

The authors studied the expression of estrogen receptor (ER) in tissues of breast carcinomas which were previously fixed in formalin and paraffin-embedded. The ER expression was correlated with several histological findings, namely grade of differentiation, tumor necrosis, desmoplasia, lymphocytic infiltration and elastosis. The ER was detected in tissues using the avidin-biotin immunoperoxidase technique associated with the H222 monoclonal antibody from Abbott. All 39 biopsies were of infiltrating ductal carcinoma of breast and 16 of them expressed ER. The statistical analysis showed that the expression of ER was correlated with histological findings of good prognosis as well differentiated carcinomas, no tumor necrosis, absence or mild lymphocytic infiltration around the tumor cells and severe elastosis.

研究了经福尔马林和石蜡包埋固定的乳腺癌组织中雌激素受体(ER)的表达。ER的表达与分化程度、肿瘤坏死、结缔组织增生、淋巴细胞浸润和弹性增生等组织学表现相关。利用亲和素-生物素免疫过氧化物酶技术结合雅培公司的H222单克隆抗体检测组织中的ER。39例活检均为乳腺浸润性导管癌,其中16例表达ER。统计分析显示,ER的表达与预后良好、分化良好、肿瘤细胞周围无坏死或轻度淋巴细胞浸润、严重弹性增生的组织学表现相关。
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引用次数: 0
期刊
Revista paulista de medicina
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