Atypical proliferative nodule in congenital melanocytic nevus with dural invasion: a case report
- Author:
Jae Hoon JUNG
1
;
Kee Taek JANG
;
Ara KIM
;
So Young LIM
Author Information
- Publication Type:Case Report
- Keywords: Dura mater; Melanocytic nevus syndrome, congenital; Neoplasm invasiveness; Tissue expansion devices
- MeSH: Child, Preschool; Diagnosis; Dura Mater; Female; Follow-Up Studies; Humans; Immunohistochemistry; Magnetic Resonance Imaging; MART-1 Antigen; Neoplasm Invasiveness; Nevus, Pigmented; Scalp; Tissue Expansion Devices
- From:Archives of Craniofacial Surgery 2019;20(2):139-143
- CountryRepublic of Korea
- Language:English
- Abstract: Here we report a case of a focal atypical proliferative nodule (PN) arising from a congenital melanocytic nevus (CMN). Diagnosis was challenging because it had both benign and malignant clinical features. Unusual histopathology, immunohistochemistry, and intraoperative findings of this atypical PN are discussed. A 5-year-old girl was admitted for a congenital 5× 5 cm sized scalp mass. This hemangioma-like soft mass showed biphasic characteristics such as a slow, gradual, and benign increase in size but worrisome dural invasion with cranial bone defect. We removed the scalp mass with clear resection margins. Interoperatively, we found that the cranial bone defect had already filled. Histopathologic examination showed CMN with focal atypical PN. The nodule showed sharp demarcation and cellular pleomorphism. However, in immunohistochemical study, Ki-67 proliferation index and expression levels of protein S-100 and Melan-A were very low. These were unusual findings of atypical PNs. Despite her worrisome preoperative radiologic features, she showed an indolent clinical course compatible with previously reported biologic behavior. The patient underwent follow-up inspection with magnetic resonance imaging every 6 months for up to 3 years. The nodule appeared to be stationary at the last visit.
