Fishman S J, Phelps R G, Lebwohl M, Lieber C
Department of Dermatology, Mount Sinai Medical Center, New York, NY 10029.
Am J Dermatopathol. 1989 Aug;11(4):369-74. doi: 10.1097/00000372-198908000-00012.
A congenital arrector pili hamartoma is a neoplasm that presents as multiple or solitary dermal nodules in a dermatomal distribution. To elucidate and clarify its histogenesis, a lesion derived from a 3-year-old boy was studied by light microscopy, indirect immunofluorescence, using antibodies against basal lamina constituents and against interstitial matrix components, and electron microscopy. In addition, a rabbit antibody specific for bovine smooth-muscle myosin was used. The antibodies against the basal lamina components and fibronectin all showed an intense perimysial fluorescence that ensheathed and surrounded individual leiomyocytes. Anti-smooth-muscle myosin exhibited intense cytoplasmic fluorescence. Furthermore, electron microscopy showed fusiform cells with abundant myofilaments, dense bodies, and pericellular basal lamina as seen in smooth muscle. These studies suggest the probable origin of this hamartoma from pili arrector muscle and could be used as an adjunct in histopathological diagnosis.
先天性竖毛肌错构瘤是一种肿瘤,表现为沿皮节分布的多个或单个真皮结节。为了阐明和明确其组织发生,我们通过光学显微镜、间接免疫荧光法(使用抗基膜成分和抗间质基质成分的抗体)以及电子显微镜对一名3岁男孩的病变进行了研究。此外,还使用了一种针对牛平滑肌肌球蛋白的兔抗体。抗基膜成分和纤连蛋白的抗体均显示出强烈的肌束膜周围荧光,该荧光包裹并环绕单个平滑肌细胞。抗平滑肌肌球蛋白显示出强烈的细胞质荧光。此外,电子显微镜显示出梭形细胞,具有丰富的肌丝、致密体和细胞周围基膜,这与平滑肌所见相同。这些研究提示该错构瘤可能起源于竖毛肌,可作为组织病理学诊断的辅助手段。