Pathology of allergic diseases.

A Schwartz
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Abstract

An allergic disease may develop in any organ or system. The respective etiological factors include foreign proteins, infectious agents such as various microbes, viruses, moulds, parasites, chemical compounds often in the form of drugs usually designated as haptens, polysaccharides, benign and malignant neoplasms. Of the factors operating in the causal pathogenesis of such diseases the most important one is an exaggerated formation of antibodies, which appears to be uncontrolled and occurring irrespective of the demands of the organism. The essential morphological features in allergic inflammation are rather variegated, their diagnostic value differing in a wide range but being never absolute. The above features include eosinophilic leucocytes, allergic arteritis and phlebitis, fibrinoid necrotic glomerulonephritis, histiocytic granulomatous inflammation or histiocytic granuloma. Granulomatous capsulitis and trabeculitis affecting the spleen and lymph nodes are believed to be of major diagnostic significance. The immunofluorescent and immunoperoxidase methods and electron microscopy are important diagnostic tools. It has been generally acknowledged that many drugs operate as antigens. They may cause death of the respective patient, but allergic manifestations may subside after withdrawal of such drugs. On occasion they operate as a trigger mechanism with the allergy progressing even after treatment had been interrupted. Therefore they have been receiving extreme attention. Our collection of cases a case of giant-cell myocarditis following sulfamethoxypyridazine, anaphylactic shock has been reported to occur after intravenous administration of novocaine, and generalized cutaneous vasculitis developed in the same patient during the subsequent phase. A similar cutaneous finding was reported to have developed after penicillin injection, granulomatous inflammation developed owing to sulfonamide treatment. Allergic tumour-like lymphadenitis developed after administration of anti-anthracic serum; an anticonvulsive syndrome developed after hydantoinate administration. The latter consisted of generalized exanthema, hepatomegaly, splenomegaly and generalized lymphadenopathy. The lymph nodes showed tumour-like lymphadenitis mimicking lymphogranuloma or reticulosis. Allergic diseases appear as either isolated organ lesions or systemic diseases. Thus, isolated and systemic polyarteritis nodosa, isolated nasal, pulmonary or systemic Wegener's granulomatosis have been recognized. Temporal arteritis has been recognized as a localized form of systemic giant-cell arteritis. The haemolytic-uraemic syndrome appears to be a milder variety of thrombotic thrombocytopenic purpura. Allergic diseases or manifestations occasionally affect two or more organs or systems.(ABSTRACT TRUNCATED AT 400 WORDS)

变态反应性疾病的病理学。
过敏性疾病可能发生在任何器官或系统。各自的病因包括外源蛋白质、感染因子如各种微生物、病毒、霉菌、寄生虫、通常以药物形式出现的化合物(通常被指定为半抗原)、多糖、良性和恶性肿瘤。在这些疾病的因果发病机制中起作用的因素中,最重要的一个是抗体的过度形成,这似乎是不受控制的,无论生物体的需求如何,都在发生。变应性炎症的基本形态学特征是相当多样化的,它们的诊断价值在很大范围内不同,但从来没有绝对的。上述特征包括嗜酸性白细胞增多、过敏性动脉炎和静脉炎、纤维蛋白样坏死性肾小球肾炎、组织细胞性肉芽肿性炎症或组织细胞性肉芽肿。肉芽肿性囊炎和小梁炎影响脾脏和淋巴结被认为是主要的诊断意义。免疫荧光法、免疫过氧化物酶法和电子显微镜是重要的诊断工具。人们普遍认为,许多药物起着抗原的作用。它们可能导致相应患者死亡,但停用此类药物后,过敏症状可能会消退。有时,即使在治疗中断后,它们也会作为过敏进展的触发机制发挥作用。因此,他们受到了极大的关注。我们收集的病例中,有一例磺胺甲氧基吡啶嗪后出现巨细胞心肌炎,静脉注射诺佛卡因后出现过敏性休克,同一患者在随后的阶段出现全身皮肤血管炎。据报道,青霉素注射后出现了类似的皮肤发现,磺胺治疗后出现肉芽肿性炎症。抗炭疽血清后出现过敏性肿瘤样淋巴结炎;一种抗惊厥症候群是在服用羟乙酸钠后出现的。后者包括全身性肿大、肝肿大、脾肿大和全身性淋巴结病。淋巴结表现为类似淋巴肉芽肿或网状病的肿瘤样淋巴结炎。过敏性疾病表现为孤立的器官病变或全身性疾病。因此,孤立性和全身性结节性多动脉炎、孤立性鼻、肺或全身性韦格纳肉芽肿病已被确认。颞动脉炎被认为是系统性巨细胞动脉炎的一种局部形式。溶血性尿毒症综合征是一种较轻的血栓性血小板减少性紫癜。过敏性疾病或表现偶尔会影响两个或多个器官或系统。(摘要删节为400字)
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