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膀胱外软斑病的细胞学诊断

Cytologic diagnosis of extravesical malacoplakia.

作者信息

Chalvardjian A, Carydis B, Cohen S

出版信息

Diagn Cytopathol. 1985 Jul-Sep;1(3):216-20. doi: 10.1002/dc.2840010309.

Abstract

Malacoplakia, a rare form of chronic granulomatous inflammation, most frequently involves the urinary tract of middle-aged women. The disease represents an unusual inflammatory response to bacteria, most commonly Escherichia coli, and probably reflects some dysfunction in the immune system of the host. We describe two cases of malacoplakia involving in one patient the vagina and in the other the perianal subcutaneous tissue and lung. In both cases, the diagnosis was made concurrently by cytology and histologic examination of tissue sections. This, in turn, led to the institution of appropriate therapy with complete resolution of the disease. In smears, the characteristic von Hansemann histiocytes are larger than alveolar macrophages. They have a reticulated granular cytoplasm that is caused by excessive accumulation of lysosomal bodies, some of which upon mineralization give rise to the pathognomonic Michaelis-Gutmann body. The latter, which is usually intracellular, can be distinguished readily from psammoma bodies and should not be confused with yeasts.

摘要

软斑病是一种罕见的慢性肉芽肿性炎症,最常累及中年女性的泌尿道。该疾病是对细菌(最常见的是大肠杆菌)的一种异常炎症反应,可能反映了宿主免疫系统的某些功能障碍。我们描述了两例软斑病病例,一例累及阴道,另一例累及肛周皮下组织和肺部。在这两例病例中,均通过组织切片的细胞学和组织学检查同时做出诊断。这进而促使采取适当治疗,疾病得以完全缓解。在涂片检查中,特征性的冯·汉塞曼组织细胞比肺泡巨噬细胞大。它们具有网状颗粒状细胞质,这是由溶酶体过度积聚所致,其中一些溶酶体矿化后形成特征性的米凯利斯-古特曼小体。后者通常位于细胞内,可轻易与砂粒体区分,且不应与酵母混淆。

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