Ito Keigo, Ansai Shin-Ichi, Saeki Hidehisa
Department of Dermatology, The Jikei University School of Medicine.
Division of Dermatology, Nippon Medical School Musashi Kosugi Hospital.
J Nippon Med Sch. 2017;84(2):79-82. doi: 10.1272/jnms.84.79.
We report a case of syringocystadenoma papilliferum (SCAP) combined with tubular papillary adenoma (TPA) arising on the chest of a 45-year-old Japanese woman. Histopathological examination revealed the characteristic findings of SCAP in the superficial part of the lesion and those of TPA in the deeper part. We reviewed the English literature about this combination. SCAP and TPA have the same cellular components, but show differences of the general structure. The combination of these two neoplasms is more frequent than expected by most dermatopathologists or pathologists. This combination is frequently seen in patients with nevus sebaceus (NS), but it is also found in patients without NS.
我们报告一例发生在一名45岁日本女性胸部的乳头状汗管囊腺瘤(SCAP)合并管状乳头状腺瘤(TPA)的病例。组织病理学检查显示,病变浅层有SCAP的特征性表现,深层有TPA的特征性表现。我们查阅了关于这种合并情况的英文文献。SCAP和TPA具有相同的细胞成分,但总体结构存在差异。这两种肿瘤的合并情况比大多数皮肤病理学家或病理学家预期的更为常见。这种合并情况在皮脂腺痣(NS)患者中很常见,但在无NS的患者中也有发现。