| CASE REPORT |
|
| Year : 2022 | Volume
: 15
| Issue : 2 | Page : 189-192 |
|
|
Solitary neurofibroma over lower lip: A rare manifestation
Shishira R Jartarkar, B Spoorthy, Sruthi Kareddy
Department of Dermatology, Venereology and Leprosy, Vydehi Institute of Medical Sciences and Research Centre, Bengaluru, Karnataka, India
Correspondence Address:
B Spoorthy
Department of Dermatology, Venereology and Leprosy, Vydehi Institute of Medical Sciences and Research Centre, 82, Near BMTC 18th Depot, Vijayanagar, Nallurhalli, Whitefield, Bengaluru 560066, Karnataka
India
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/JCAS.JCAS_100_21
|
|
|
Neurofibromas are common nerve sheath tumors, occurring either sporadically or associated with Von Recklinghausen’s disease. Only 6.5% of solitary lesions are seen to involve the oral cavity without any features of neurofibromatosis type 1 (NF-1). It presents as a soft, skin-colored nodule with a characteristic buttonhole invagination. Histologically, it is an unencapsulated lesion consisting of proliferated neural elements, with a background of mucin and mast cells. Surgical excision is the treatment of choice. A 49-year-old female patient presented with a 35-year history of single, asymptomatic lesion over the lower lip, with no features of NF-1. On the basis of the history, histopathological findings, and dermoscopy, a diagnosis of neurofibroma was made and the lesion was excised, with no recurrence over a period of 1 year. The present case report has been reported for its interesting presentation and unusual site of involvement. |
|
|
|
| [FULL TEXT] [PDF]* |
|
 |
|
