Suzuki Shuji, Al-Hajjaj Shatha, Lee Margaret, Bhawan Jag
Dermatopathology Section, Department of Dermatology, Boston University School of Medicine, Boston, Massachusetts.
Dermatol Online J. 2018 Apr 14;24(4):13030/qt78p5v0dd.
It is relatively rare to find syringocystadenoma papilliferum (SCAP) outside the head and neck region and extremely rare in the anogenital area. Characteristic histological features such as cystic invaginations, glandular epithelium showing decapitation secretion, and stroma with plasma cells are important for making the diagnosis. We present a rare case of SCAP on the mons pubis of a 13-year-old girl and compare cases of SCAP from other rare locations.
在头颈部区域以外发现乳头状汗管囊腺瘤（SCAP）相对少见，而在肛门生殖器区域极为罕见。其特征性组织学表现，如囊性内陷、显示断头分泌的腺上皮以及含有浆细胞的间质，对于诊断至关重要。我们报告了一例13岁女孩阴阜部的罕见SCAP病例，并与其他罕见部位的SCAP病例进行比较。
