Ogi H, Kiryu H, Hori Y, Fukui M
Department of Dermatology, Masuda Red Cross Hospital, Japan.
Am J Dermatopathol. 1995 Dec;17(6):599-602. doi: 10.1097/00000372-199512000-00013.
A rare case of cutaneous skin metastasis from an intracranial chordoma is presented. A large nodule developed in the left thigh of a 22-year-old woman who had been previously diagnosed to have a chordoma at the base of her skull. Sections from the biopsied specimens of the nodule showed proliferations of physaliphorous cells and stellate cells in cords and in nests in a myxoid stroma. Immunohistochemically, neoplastic cells were stained positively with antibodies to S-100 protein and cytokeratin. The results of the histopathological and immunohistochemical studies of the nodule were interpreted as pointing to a diagnosis of metastatic chordoma based on their similarity to the results of studies of the primary neoplasm in the cranial region. Based on the number of cases of skin metastasis from chordoma reported in the literature, skin should be kept in mind as one of the target organs, although such metastases are still rare.
本文报告了一例罕见的颅内脊索瘤皮肤转移病例。一名22岁女性左大腿出现一个大结节,该女性之前被诊断为颅底脊索瘤。结节活检标本切片显示在黏液样基质中,泡状细胞和星状细胞呈条索状和巢状增生。免疫组化显示,肿瘤细胞对S-100蛋白和细胞角蛋白抗体呈阳性染色。根据结节的组织病理学和免疫组化研究结果与颅部原发性肿瘤的研究结果相似,将其解释为转移性脊索瘤的诊断依据。根据文献报道的脊索瘤皮肤转移病例数量,尽管这种转移仍然罕见,但皮肤应被视为靶器官之一。