Heustis D G, Bull B S, Hadley G G
Arch Pathol Lab Med. 1977 May;101(5):239-42.
We examined the ultrastructure of the spleen surgically removed from a patient with the in vivo diagnosis of malignant histiocytosis. The findings showed sinuses greatly dilated and lined by large atypical histiocytic cells. Erythrophagocytosis was prominent. These findings, as well as the histologic features of the bone marrow and later autopsy specimens, confirmed the diagnosis of malignant histiocytosis. The somewhat unusual confinement of histiocytes to sinusoids raised the possibility that this may represent a rare subvariant, histiocytic sinus reticulosis, first described by Robb-Smith in his original paper.
我们检查了一名活体诊断为恶性组织细胞增多症患者手术切除脾脏的超微结构。结果显示脾窦明显扩张,内衬大量非典型组织细胞。红细胞吞噬现象显著。这些发现以及骨髓和后来尸检标本的组织学特征,证实了恶性组织细胞增多症的诊断。组织细胞局限于脾窦的情况有些不寻常,这增加了一种可能性,即这可能代表一种罕见的亚型——组织细胞性窦状隙网状细胞增多症,最初由罗布 - 史密斯在其原始论文中描述。