Departments of Ophthalmology and Ocular Pathology, Emory University School of Medicine, Atlanta, Georgia, USA.
Departments of Ophthalmology and Ocular Pathology, Emory University School of Medicine, Atlanta, Georgia, USA; Oncology and Pathology Service, St. Erik Eye Hospital, Stockholm, Sweden.
Surv Ophthalmol. 2019 Nov-Dec;64(6):852-857. doi: 10.1016/j.survophthal.2019.04.002. Epub 2019 Apr 9.
Neurothekeomas (NTKs) are benign soft tissue tumors most commonly occurring in the head, neck, and upper extremities of young adults, with a female preponderance. Herein, we report 2 cases of ocular NTK presenting as an orbital mass or chalazion. Both cases underwent excision of the mass with histopathologic diagnosis of cellular NTK. Tumor cells for both cases were immunopositive for smooth muscle actin, microphthalmia-associated transcription factor, and cluster of differentiation 10. S100, human melanoma black 45, and melanoma antigen recognized by t-cell (Melan A) were negative. Both were associated with scattered histiocytes, which were positive for cluster of differentiation 68. To date, including our 2 cases, there have been 22 cases of ocular and periorbital adnexal NTK reported in the English-language literature. Although rare, clinicians should include NTK in their differential diagnosis in patients presenting with a periocular soft tissue tumor.
神经鞘瘤(NTKs)是一种常见的良性软组织肿瘤,主要发生于青年患者的头颈部和上肢,女性多见。本文报告了 2 例眼部 NTK,表现为眶内肿块或霰粒肿。2 例患者均行肿块切除术,组织病理学诊断为细胞性 NTK。2 例肿瘤细胞均免疫阳性表达平滑肌肌动蛋白、小眼畸形相关转录因子和分化群 10。S100、人黑色素瘤黑 45 和 T 细胞识别的黑色素瘤抗原(Melan A)均为阴性。均伴有散在的组织细胞,其分化群 68 阳性。迄今为止,包括我们的 2 例病例,在英文文献中已经报道了 22 例眼部和眼眶附属器 NTK。虽然罕见,但临床医生在遇到眶周软组织肿瘤的患者时,应将 NTK 纳入鉴别诊断。