Ghanadan Alireza, Khosravi Mohsen
Department of Dermatopathology, Autoimmune Bullous Diseases Research Center, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Indian J Dermatol. 2013 Jul;58(4):326. doi: 10.4103/0019-5154.113956.
Syringoma is a benign adnexal tumor derived from intraepidermal eccrine duct.
The aim of the study is to report the experience concerning syringoma by reviewing the clinical and histopathologic features of a series of 34 histologically diagnosed syringoma patients observed over a period of six years.
Thirty-four patients were sorted into two groups, localized and generalized syringoma, according to the Friedman and Butler classification. Different histopathologic findings were recorded in specially designed questionnaires for further analysis.
Ninety-seven percent of the patients were females with the mean age of 27.6 years. The mean duration of the lesions before the presentations was six years. The diagnosis of syringoma was only considered in 23 patients (67.6%) and was the initial diagnosis in only 13 (38.2%) patients. All histological findings were seen more common in our cases. in comparison to the documented cases in the literature. Clear cell change of epithelial eccrine cells was 85.2% and there was no difference in the histopathological findings in the two groups. Our patients with generalized syringoma (GS) had a considerable lower age of onset than the ones with localized syringoma (LS) (P = 0.027).
Our patients with generalized syringoma were younger than the ones with localized syringoma. Distribution of the generalized syringoma was mainly in the chest and neck followed by the forearms whereas localized syringoma was mostly confined to the face, axilla and genitalia. There were also some conditions associated with our cases including sarcoidosis, calcinosis cutis and basal cell carcinoma.
汗管瘤是一种源自表皮内小汗腺导管的良性附属器肿瘤。
本研究旨在通过回顾6年期间观察的34例经组织学诊断为汗管瘤患者的临床和组织病理学特征,报告有关汗管瘤的经验。
根据弗里德曼和巴特勒分类法,将34例患者分为两组,即局限性汗管瘤和泛发性汗管瘤。将不同的组织病理学结果记录在专门设计的问卷中以供进一步分析。
97%的患者为女性,平均年龄27.6岁。皮损出现前的平均病程为6年。仅23例患者(67.6%)考虑诊断为汗管瘤,仅13例(38.2%)患者为初诊。与文献记载的病例相比,所有组织学结果在我们的病例中更为常见。上皮小汗腺细胞的透明细胞改变为85.2%,两组的组织病理学结果无差异。泛发性汗管瘤(GS)患者的发病年龄明显低于局限性汗管瘤(LS)患者(P = 0.027)。
我们的泛发性汗管瘤患者比局限性汗管瘤患者年轻。泛发性汗管瘤主要分布于胸部和颈部,其次是前臂,而局限性汗管瘤大多局限于面部、腋窝和生殖器。我们的病例还伴有一些相关疾病,包括结节病、皮肤钙质沉着和基底细胞癌。