Yang Ya-Wen, Shih I-Hsin, Huang Yu-Huei, Kuo Tseng-Tong, Hong Hong-Shang
Department of Dermatology, Chang Gung Memorial Hospital, Taipei, Taiwan.
Dermatol Surg. 2005 Jun;31(6):720-2. doi: 10.1111/j.1524-4725.2005.31623.
Neurothekeoma is a rare cutaneous neoplasm, often occurring as a nondescript cutaneous nodule on the central face, shoulders, and upper extremities.
To present a patient with mixed-type neurothekeoma with an unusual clinical presentation.
We report a 29-year-old female who developed an asymptomatic, red, dermal nodule with satellite papules on the back over a period of 6 months.
The coalescing papules on the back were excised, and the histopathology and immunohistochemical study revealed a mixed-type neurothekeoma.
Neurothekeoma usually presents with a small, solitary, and slow-growing nodule or papule on the upper body. The case is interesting because of the unusual clinical manifestation of one dermal tumor with several satellite lesions.
神经鞘黏液瘤是一种罕见的皮肤肿瘤,常表现为中央面部、肩部和上肢的不典型皮肤结节。
报告1例具有不寻常临床表现的混合型神经鞘黏液瘤患者。
我们报告1例29岁女性,在6个月内背部出现一个无症状的红色真皮结节及卫星状丘疹。
切除背部融合的丘疹,组织病理学和免疫组化研究显示为混合型神经鞘黏液瘤。
神经鞘黏液瘤通常表现为上半身的小的、孤立的、生长缓慢的结节或丘疹。该病例因一个真皮肿瘤伴有多个卫星病灶的不寻常临床表现而有趣。