Kage M, Nakamura Y, Ozumi K
Department of Pathology, Saint Mary's Hospital, Kurume, Japan.
Acta Pathol Jpn. 1990 Jun;40(6):431-4. doi: 10.1111/j.1440-1827.1990.tb01583.x.
We report a rare case of apocrine neoplasm with malignant potential. The patient, a 29-year-old man, had a nodule 1 cm in diameter on his left upper eyelid which had been growing slowly for several years. It was a cystic lesion, consisting of neoplastic cells of probable apocrine gland or Moll's gland origin. This opinion was based on the histological characteristics, which included eosinophilic cytoplasm accompanied with decapitation secretion, iron granules, and granular depositions which were stained positively with periodic acid-Schiff, with and without diastase digestion. Ferritin was found in their cytoplasm, a feature that has not been reported. It was uncertain whether the neoplasm was benign or malignant, because the cells showed nuclear atypia, characterized by variation in size and hyperchromasia, but lacked the histological features of malignancy, including infiltration into the adjacent tissue and mitosis.
我们报告一例罕见的具有恶性潜能的顶泌汗腺肿瘤。患者为一名29岁男性,左上眼睑有一个直径1厘米的结节,已缓慢生长数年。这是一个囊性病变,由可能起源于顶泌汗腺或Moll腺的肿瘤细胞组成。这一观点基于组织学特征,包括嗜酸性细胞质伴有断头分泌、铁颗粒以及经高碘酸-希夫染色呈阳性的颗粒状沉积物,有无淀粉酶消化均如此。在其细胞质中发现了铁蛋白,这一特征此前未见报道。肿瘤是良性还是恶性尚不确定,因为细胞显示出核异型性,其特征为大小不一和核深染,但缺乏恶性的组织学特征,包括浸润邻近组织和有丝分裂。