Bouton C, Herson S, Huchon G, Akoun G
Poumon Coeur. 1976;32(4):153-9.
The bronchiolo-alveolar adenocarcinoma, less frequent than other types of bronchopulmonary cancers, occurs more frequently during pulmonary fibrosis. Besides a mucous bronchorrhea of little meaning, the clinical manifestations belong to the advanced stages. The X-ray, unreliable and variable, shows a variety of pictures from mono or multinodular ones to pseudopneumonic infiltrates. Usually no information could be derived from bronchoscopy. Positive cytological examination of sputum are unfrequent. Early surgery brings longer remissions than in other types of bronchopulmonary cancer. Diagnosis can only be made from the histology of the exeresis sample. The tumour cells, cuboidal or columnar, are arranged in mono or pluri-stratified layers in the inter-alveolar septa, which progressively become fibrous. This cancer has an original histogenesis: it would originate from the neoplastic metaplasia of type II pneumocytes or of respiratory bronchiole cells, invading the pulmonary alveoli by sliding or by contiguity. Far from the initial foyer, the spreading seems mostly done through airways.
细支气管肺泡腺癌比其他类型的支气管肺癌发病率低,在肺纤维化时更常发生。除了意义不大的粘液性支气管溢外,临床表现多属于晚期。X线表现不可靠且多变,显示出从单结节或多结节到假肺炎性浸润等多种影像。通常支气管镜检查无法提供有用信息。痰细胞学检查阳性并不常见。早期手术带来的缓解期比其他类型的支气管肺癌更长。诊断只能通过切除标本的组织学检查来确定。肿瘤细胞呈立方形或柱状,在肺泡间隔内呈单层或多层排列,肺泡间隔逐渐纤维化。这种癌症有独特的组织发生学:它可能起源于II型肺泡上皮细胞或呼吸性细支气管细胞的肿瘤化生,通过滑动或相邻方式侵犯肺泡。远离初始病灶时,扩散似乎主要通过气道进行。