Nihei K, Terashima K, Nito T, Imai Y, Aoyama K, Takahashi K, Ando H, Koike K, Sasaki H
Acta Pathol Jpn. 1984 Jan;34(1):159-68. doi: 10.1111/j.1440-1827.1984.tb02195.x.
Tumor forming acute promyelocytic leukemia (APL) is rare and only three cases have been documented. However, there are no reports on either the chloromatous character or electron microscopical analysis. The present paper dealt with a light, electron microscopic and histochemical study of the tumor of APL in a 55-year-old Japanese male. The tumors found in the anterior mediastinum and right lower extremity. He died from respiratory disturbance and hydrothorax due to obstruction of the pulmonary truncus by the mediastinal tumor. In electron microscopy, the tumor cells showed dilatation, colloracious pattern and honey-comb-like structure of rough endoplasmic reticula (RER) and parallel array-arrangement of smooth endoplasmic reticula (SER). These abnormalities of ER are the same as those recently recognized in leukemic cells in APL. Furthermore, the intercellular junctions composed of opposing dense patches of the cytoplasmic plasmalemma were frequently found between the more immature tumor cell of the mediastinum.
肿瘤形成性急性早幼粒细胞白血病(APL)较为罕见,仅有3例文献记载。然而,关于其绿色瘤特征或电子显微镜分析均无报道。本文对一名55岁日本男性的APL肿瘤进行了光镜、电镜及组织化学研究。肿瘤位于前纵隔和右下肢。他因纵隔肿瘤阻塞肺动脉干死于呼吸障碍和胸腔积液。在电子显微镜下,肿瘤细胞显示粗面内质网(RER)扩张、着色模式及蜂窝状结构,滑面内质网(SER)呈平行排列。内质网的这些异常与最近在APL白血病细胞中发现的相同。此外,在纵隔中较不成熟的肿瘤细胞之间经常发现由细胞质质膜相对致密斑组成的细胞间连接。