Department of Pathology, The Ohio State University Wexner Medical Center, James Cancer Hospital and Solove Research Institute, Columbus, Ohio.
Department of Pathology, The Ohio State University Wexner Medical Center, James Cancer Hospital and Solove Research Institute, Columbus, Ohio.
J Am Soc Cytopathol. 2022 Sep-Oct;11(5):274-280. doi: 10.1016/j.jasc.2022.05.002. Epub 2022 May 10.
Eccrine spiradenoma (ES) is a rare benign cutaneous adnexal tumor. The aim of our study was to discuss the clinical presentation, cytomorphologic features, and differential diagnosis of a series of 3 cases of ES diagnosed by fine needle aspiration (FNA).
The pathology databases were searched for cases of ES diagnosed by FNA and confirmed by follow-up surgical excision. FNA smears, cell blocks, and histologic sections were examined.
Three cases of ES that had presented as a soft tissue mass from 3 patients were reviewed. The sites included the left forearm, left leg, and left ankle. Cytology smears showed the presence of hypercellular 3-dimensional dense cell clusters and smaller loose cell aggregates, single cells, and bare nuclei. Most cells had round to oval nuclei, scant cytoplasm, and indistinct cell borders. A second population of cells had more spindled nuclei and were often dispersed as single cells. Scattered lymphocytes were present. Two cases showed the presence of pseudo-rosettes composed of hyaline globules of basement membrane-like material with a surrounding row of basaloid cells. None of the cases showed cytologic atypia, necrosis, or mitoses. Immunohistochemistry was used in 2 cases and showed positive staining with myoepithelial markers (smooth muscle actin, calponin, S100, and CK5). The cytology diagnoses were ES, basaloid cutaneous adnexal neoplasm, and suspicious for ES.
FNA cytopathology of ES demonstrated banal basaloid and spindle cells, lymphocytes, and infrequent metachromatic-stained hyaline globules. A specific diagnosis requires immunohistochemistry testing to avoid confusion with other cutaneous basaloid neoplasms.
小汗腺螺旋腺瘤(ES)是一种罕见的良性皮肤附属器肿瘤。我们的研究目的是通过细针抽吸(FNA)诊断的 3 例 ES 病例,讨论其临床表现、细胞学特征和鉴别诊断。
在病理数据库中搜索通过 FNA 诊断并通过后续手术切除证实的 ES 病例。检查了 FNA 涂片、细胞块和组织学切片。
回顾了 3 例来自 3 名患者的表现为软组织肿块的 ES 病例。病变部位包括左前臂、左小腿和左踝。细胞学涂片显示存在细胞丰富的三维密集细胞簇和较小的疏松细胞聚集、单个细胞和裸核。大多数细胞具有圆形至椭圆形核、稀少的细胞质和不明显的细胞边界。第二类细胞具有更多梭形核,通常呈单个细胞分散。散在的淋巴细胞存在。2 例显示存在由基底膜样物质的透明小球组成的假玫瑰花结,周围有一排基底样细胞。没有病例显示细胞异型性、坏死或有丝分裂。2 例进行了免疫组织化学检查,显示肌上皮标志物(平滑肌肌动蛋白、钙调蛋白、S100 和 CK5)阳性染色。细胞学诊断为 ES、基底细胞型皮肤附属器肿瘤和疑似 ES。
ES 的 FNA 细胞学表现为普通的基底样和梭形细胞、淋巴细胞和罕见的变色透明小球。明确诊断需要免疫组织化学检查,以避免与其他皮肤基底细胞肿瘤混淆。