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[Mutations of mitochondrial DNA and their relation to neuromuscular diseases]. [线粒体DNA突变及其与神经肌肉疾病的关系]。
V Wunderlich

According to present knowledge, mutations of mitochondrial DNA (mtDNA), implicated in the mitochondrial theory of carcinogenesis that had been inaugurated 50 years ago by Graffi, appear to be involved in malignant transformation of cells, although no definite evidence has been provided, as yet. However, as very recently elucidated, a clear-cut association exists between different classes of mutations of mtDNA (among them point mutations, deletions and duplications) and some human mitochondriopathies, particularly neuromuscular diseases. These include Leber's hereditary optic neuropathy, the Kearns-Sayre syndrome and two encephalomyopathies known by the acronyms MERRF and MELAS syndrome. The different alterations of mtDNA, though variable, can be assigned to defined positions on the genetic map of mtDNA. Point mutations of mtDNA seem to occur preferentially in conjunction with maternally inherited disorders. Although the results obtained so far are of interest mainly in terms of cognitive theory they provide new stimuli for the development of molecular diagnosis, genetic counselling and possibly for more effective treatment of the above diseases.

根据目前的知识,线粒体DNA (mtDNA)的突变与50年前由Graffi创立的线粒体致癌理论有关,似乎参与了细胞的恶性转化,尽管尚未提供明确的证据。然而,正如最近阐明的那样,不同类别的mtDNA突变(其中包括点突变、缺失和重复)与一些人类线粒体疾病,特别是神经肌肉疾病之间存在明确的关联。这些疾病包括利伯氏遗传性视神经病变,卡恩斯-塞尔综合征和两种脑肌病,简称为MERRF和MELAS综合征。mtDNA的不同改变,虽然是可变的,但可以分配到mtDNA遗传图谱上的定义位置。mtDNA的点突变似乎优先与母系遗传疾病一起发生。虽然到目前为止获得的结果主要是在认知理论方面,但它们为分子诊断、遗传咨询和可能更有效地治疗上述疾病的发展提供了新的刺激。
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引用次数: 0
[Non-Hodgkin's lymphoma of the thyroid gland. Morphologic and immunohistochemical findings in 2 cases]. 甲状腺非霍奇金淋巴瘤。形态学及免疫组化结果2例]。
I Michailov, A Popov, I Valkov, B Alexiev

Described in this paper are two cases of non-Hodgkin lymphoma (NHL) of the thyroid gland in women with Hashimoto's thyroiditis. NHL may be misinterpreted for its histological similarity to anaplastic thyroid carcinoma. The immunoperoxidase technique can be used with good success to confirm the lymphocytic origin of tumor cells.

本文报告两例患桥本甲状腺炎的女性甲状腺非霍奇金淋巴瘤(NHL)。NHL可能因其与间变性甲状腺癌的组织学相似而被误解。免疫过氧化物酶技术可以很好地证实肿瘤细胞的淋巴细胞起源。
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引用次数: 0
[The nosological situation of hereditary motor and sensory neuropathies (HMSN, Charcot-Marie-Tooth disease, neural muscular atrophy)]. [遗传性运动和感觉神经病变(HMSN、腓骨肌萎缩症、神经性肌萎缩症)的分类学情况]。
R Warzok, B Wattig, G Schwesinger, H Schneeweiss, F Heydenreich

Hereditary motor and sensory neuropathies (HMSN) comprise a heterogeneous group of disorders. Since phenotypic manifestations are similar in most families, classification is based on differences in the mode of inheritance, onset and progression of the disease, nerve conduction velocity and nerve biopsy findings. Autosomal dominant, autosomal recessive, X-dominant and X-recessive forms, substantial intrafamilial differences, intermediate forms and the combination of neuropathies with spinocerebellar degeneration within one and the same sibship have been described. On the basis of selected own cases it is demonstrated that there is a broad spectrum of functional and structural abnormalities depending on the progression of the disease and on the site of nerve studied (proximal or distal part). Both the neuronal and hypertrophic variants begin with axonal degeneration of the dying back type followed by segmental demyelination and variable degrees of hypertrophic Schwann cell proliferation. Constantly, posterior columns of the spinal cord reveal fiber loss. Since the molecular basis of the different forms remains to be clarified it seems to be of greater interest to underline common features than to separate seemingly different nosological entities. It is suggested that the latter are partly the result of a selection of cases with a variable severity. Evidently, the syndrome of myatrophic ataxia comprises apart from "pure" HMSN with unsignificant degenerations of posterior columns and "pure" Friedreich's ataxia with mild peripheral nerve fiber loss intermediate forms.

遗传性运动和感觉神经病变(HMSN)包括一组异质性的疾病。由于大多数家族的表型表现相似,因此分类是基于遗传方式、疾病的发生和进展、神经传导速度和神经活检结果的差异。常染色体显性,常染色体隐性,x -显性和x -隐性形式,大量的家族内差异,中间形式和神经病变合并脊髓小脑变性在一个和同一兄弟姐妹中被描述。在选择自己的病例的基础上,它证明了根据疾病的进展和所研究的神经部位(近端或远端),存在广泛的功能和结构异常。神经性和增生性变异体均以死背型的轴突变性开始,随后是节段性脱髓鞘和不同程度的增生性雪旺细胞增殖。脊髓后柱经常显示纤维丢失。由于不同形式的分子基础仍有待澄清,因此强调共同特征似乎比分离看似不同的病分学实体更有兴趣。有人认为,后者在一定程度上是对严重程度不同的病例进行选择的结果。显然,肌萎缩性共济失调综合征除了“纯粹的”HMSN伴后柱不明显变性外,还有“纯粹的”friedrich’s共济失调伴轻度周围神经纤维丧失的中间形式。
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引用次数: 0
[Fibrolamellar variant of hepatocellular carcinoma]. [肝细胞癌纤维板层变异型]。
J Důra, A Linhartová

A fibrolamellar variant of hepatocellular carcinoma with metastases in 2 regional lymph nodes was surgically removed from a girl, 17 years of age. This type of tumor has a typical histological pattern. Prognosis is found to be better than that of the common hepatocellular carcinoma.

一个17岁的女孩手术切除了2个区域淋巴结转移的纤维板层型肝细胞癌。这种肿瘤具有典型的组织学特征。预后优于普通肝细胞癌。
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引用次数: 0
[Problems of agreement between clinical and autopsy diagnoses. Reply to the comments of Schneider and coworkers]. 临床诊断与尸检诊断一致的问题。回复施耐德和同事的意见]。
F Vollmar
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引用次数: 0
[Nuclear bridges and nodes in the mature human placenta]. [成熟人类胎盘中的核桥和核节点]。
T Wepler

Series of semi-thin sections were prepared of mature human placentas after immersion and perfusion fixation. Evidence was produced to the existence of syncytial bridges between neighbouring chorionic villi. Besides, syncytial knots and sprouts were present, as well as structures apparently similar to bridges which had resulted from peculiar cutting through a syncytial knot. The latter have been referred to as artefacts by other authors and are obtainable only under two conditions: 1. pre-existence of nuclear agglomeration at cutting level; 2. accidentally appropriate cutting. Such coincidence has been recordable from two thirds of all cases, but it is by no means responsible for all cases of bridge formation. Structures of that kind are never artefacts by any account of lexical meaning. The following criteria are suggested for differentiation between bridges, on the one hand, and structures resembling bridges due to tangential sections: 1. Number of nuclei relative to bridge surface; 2. Limitation of surface; 3. Appearance and arrangement of nuclei.

将人成熟胎盘经浸泡和灌注固定后,制备了一系列半薄切片。证据表明相邻的绒毛膜绒毛之间存在合胞桥。此外,存在合胞结和芽,以及明显类似于桥的结构,这是由于合胞结的特殊切割造成的。后者被其他作者称为人工制品,只有在两个条件下才能获得:1。切割水平核团聚的预先存在;2. 不小心适当的切割。这种巧合在三分之二的情况下都是可记录的,但绝不是所有桥型形成的原因。从词汇意义上讲,这种结构从来不是人工制品。对于桥梁和由于切向截面而类似于桥梁的结构,建议采用以下标准进行区分:相对于桥表面的核数;2. 表面限制;3.细胞核的外观和排列。
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引用次数: 0
[Pathology of the placenta. I. Preliminary anatomic remarks, microscopic findings and sampling of material]. 胎盘的病理学。1 .初步解剖注释,显微发现和材料取样]。
P Emmrich

The first part of this review of pathological aspects relating to the placenta is made up of introductory comments on the material that is subject of histological investigation as well as on clinical questions and a thorough description of macroscopic findings. Hints are also given on collection of placental samples and histological investigation. The coverage is completed by a few comments on the normal anatomy of the placenta.

与胎盘有关的病理方面的回顾的第一部分是由对材料的介绍性评论组成的,这些材料是组织学调查的主题,也是对临床问题和宏观发现的彻底描述。提示胎盘标本的收集和组织学调查。覆盖是完成了一些评论的正常解剖的胎盘。
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引用次数: 0
[Problems of the agreement of clinical and postmortem diagnoses. Comment on the article by F. Vollmar (Zentralbl. allg. Pathol. pathol. Anat. 1989; 135:699-704)]. [临床和尸检诊断的一致性问题。F.Vollmar的文章评论(Zentralbl.allg.Pathol.Pathol.Anat.1989;135:699-704)]。
E Schneider, H Behrendt, T Wegner
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引用次数: 0
[The immunologic situation of the placenta and its significance for disorders in early pregnancy]. 【胎盘免疫状况及其对妊娠早期疾病的意义】。
L C Horn, M Rosenkranz, K Bilek

Reference is made in numerous recent immunological studies to immunological mechanisms which were found to play a role in acceptance of pregnancy or habitual abortions. The most important theories likely to offer explanations for these phenomena are reviewed in some detail, including hormonal immunosuppression, immunologic-anatomic barrier at the placenta as well as blocking factors and anti-sperm antibodies. Molar pregnancy is associated with a particular immunological situation. None of the theories mentioned can be preferred, for the time being, to explain acceptance of normal pregnancy or the causes of recurrent spontaneous abortions.

在最近的许多免疫学研究中,人们发现免疫机制在接受怀孕或习惯性流产中起着重要作用。本文对可能解释这些现象的最重要的理论进行了详细的回顾,包括激素免疫抑制、胎盘免疫解剖屏障以及阻断因子和抗精子抗体。磨牙妊娠与一种特殊的免疫状况有关。目前,上述任何一种理论都不能用来解释接受正常妊娠或反复自然流产的原因。
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引用次数: 0
[Dihydralazine hepatitis. Morphologic and clinical criteria for diagnosis]. [Dihydralazine肝炎。诊断的形态学和临床标准]。
G Roschlau, R Baumgarten, J D Fengler

70 cases of acute dihydralazine-associated hepatitis with centrolobular or confluent necroses, registered in the files of the Berlin-Friedrichshain Institute of Pathology, between 1981 and 1985, were classified into 3 types of diagnostic probability for differential diagnosis versus virus hepatitis. Classification was conducted according to recommendations given by a working group of pathologists, specialised in liver pathology. 42 cases out of this material had come from Prenzlauer-Berg Hospital, Department of Infectious Diseases, and were re-examined under clinical aspects. 6 of them were discarded from evaluation. Type I proved to be of high diagnostic reliability, as was seen from 61% of all cases. Only 3 cases had to be discarded from that group and were associated with other drugs, such as halothane, methyldopa, and propranolol. The following clinical parameters proved to be of particular value for definite assessment of drug-induced hepatitis: time of exposure (for analysis of co-medication), time of recovery, and re-exposure test. Only circumstantial evidence so far can be provided for all histological types to causative relationship between drug ingestion and hepatitis. Compliance with mandatory notification should be ensured in all cases, since suspicious cases are explicitly included. Higher sex-related disposition of women to drug-induced hepatitis was confirmed in our material, with the female-to-male ratio being 3:1.

1981年至1985年,在柏林弗里德里希斯海因病理研究所登记的70例急性二羟嗪相关性肝炎伴中央小叶或合流性坏死,根据诊断概率与病毒性肝炎的鉴别诊断分为3种类型。分类是根据专门从事肝脏病理学的病理学家工作组的建议进行的。这些材料中的42例来自普伦茨劳贝格医院传染病科,并在临床方面进行了重新检查。其中6例退出评价。从61%的病例中可以看出,I型被证明是高诊断可靠性的。该组中仅有3例患者需弃用其他药物,如氟烷、甲基多巴、心得安等。以下临床参数被证明对药物性肝炎的明确评估有特别的价值:暴露时间(用于分析联合用药)、恢复时间和再次暴露试验。到目前为止,所有组织学类型的药物摄入与肝炎之间的因果关系只能提供间接证据。应确保在所有情况下都遵守强制性通知,因为可疑情况已明确包括在内。我们的资料证实,女性对药物性肝炎的性别倾向较高,男女比例为3:1。
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Zentralblatt fur allgemeine Pathologie u. pathologische Anatomie
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