Vital C, Vital A, Lagueny A, Larribau E, Saintarailles J, Julien J
Neuropathology Laboratory, Victor Segalen University, Bordeaux, France.
Ultrastruct Pathol. 1998 Sep-Oct;22(5):377-83. doi: 10.3109/01913129809103359.
Inflammatory polyneuropathies are mainly known by their acute form, Guillain-Barré syndrome, but there are also chronic cases and all are considered as having an autoimmune mechanism. In each form, peripheral nerve biopsies show scattered macrophages in the endoneurium and in certain cases macrophages invade the Schwann cell cytoplasm and destroy the myelin sheath. In rarer cases there is a primary axonal degeneration. The authors studied two chronic cases, which both exhibited mixed primitive axonal and demyelinating lesions, with peculiar histiocytes in the endoneurium. These rounded cells were characteristically well marked by KP1 but showed well-developed rough endoplasmic reticulum cysternae at ultrastructural examination. Such plasmacytoid histiocytes have mainly been studied in subacute lymphadenopathies and have been only briefly illustrated in a few cases of peripheral neuropathies due to Lyme disease or HIV infection. The two cases reported here had no associated diseases and probably correspond to a peculiar subacute autoimmune reaction.
炎性多发性神经病主要以其急性形式格林-巴利综合征而为人所知,但也有慢性病例,并且所有病例都被认为具有自身免疫机制。在每种形式中,周围神经活检显示神经内膜中有散在的巨噬细胞,在某些情况下巨噬细胞侵入施万细胞胞质并破坏髓鞘。在较罕见的情况下会出现原发性轴突变性。作者研究了两例慢性病例,这两例均表现为混合性原发性轴索和脱髓鞘病变,神经内膜中有特殊的组织细胞。这些圆形细胞特征性地被KP1标记良好,但在超微结构检查中显示有发育良好的粗面内质网池。这种浆细胞样组织细胞主要在亚急性淋巴结病中进行过研究,在少数莱姆病或HIV感染所致周围神经病病例中仅有简要描述。此处报告的这两例病例无相关疾病,可能对应一种特殊的亚急性自身免疫反应。