Malignant Cutaneous Neurocristic Hamartoma With Features of Melanoma: A Rare Entity.

malignant cutaneous neurocristic hamartomas malignant neurocristic hamartomas melanocytic lesion neurocristic cutaneous hamartoma neurocristic hamartoma

Journal

Cureus
ISSN: 2168-8184
Titre abrégé: Cureus
Pays: United States
ID NLM: 101596737

Informations de publication

Date de publication:
Sep 2024
Historique:
accepted: 15 09 2024
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 18 10 2024
Statut: epublish

Résumé

Neurocristic cutaneous hamartoma (NCH) is a rare, benign neoplastic skin lesion characterized by a combination of neuroectodermal and mesodermal components. Clinically, NCH typically presents as asymptomatic, well-circumscribed, and elevated cutaneous nodules. Histopathologically, it is characterized by nests of pigmented melanocytes and varying degrees of fibrosis and collagen deposition. The precise etiology of NCH remains undetermined; however, it is hypothesized to arise from the aberrant development of neuromesenchyme. Due to its potential to mimic other pigmented melanocytic disorders, accurate differential diagnosis is crucial to prevent mismanagement. Surgical excision is the preferred treatment modality, offering a generally favorable prognosis and low recurrence rate. Conversely, malignant cutaneous neurocristic hamartoma (MCNH), an exceedingly rare malignant variant of NCH, poses a significantly different clinical challenge. This review focuses on the diagnostic criteria, clinical presentation, and management strategies for MCNH, emphasizing the need for differentiation from other similar cutaneous lesions. We present a detailed case report of MCNH in a 56-year-old female, highlighting its histopathological and immunohistochemical features to provide insights into the diagnosis and therapeutic approach for this exceptionally rare malignancy.

Identifiants

pubmed: 39421096
doi: 10.7759/cureus.69594
pmc: PMC11484887
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Pagination

e69594

Informations de copyright

Copyright © 2024, Tahir et al.

Déclaration de conflit d'intérêts

Human subjects: Consent was obtained or waived by all participants in this study. Conflicts of interest: In compliance with the ICMJE uniform disclosure form, all authors declare the following: Payment/services info: All authors have declared that no financial support was received from any organization for the submitted work. Financial relationships: All authors have declared that they have no financial relationships at present or within the previous three years with any organizations that might have an interest in the submitted work. Other relationships: All authors have declared that there are no other relationships or activities that could appear to have influenced the submitted work.

Auteurs

Muhammad Tahir (M)

Pathology and Laboratory Medicine, University of South Alabama College of Medicine, Mobile, USA.

Abdulhadi Samman (A)

Basic Medical Sciences, Pathology Division, College of Medicine, University of Jeddah, Jeddah, SAU.

Sara Shalin (S)

Pathology, University of Arkansas for Medical Sciences, Arkansas, USA.

Kurt Knowles (K)

Pathology and Laboratory Medicine, University of South Alabama College of Medicine, Mobile, USA.

Guillermo A Herrera (GA)

Pathology, University of South Alabama College of Medicine, Mobile, USA.

Joe S Liles (JS)

Surgery, University of South Alabama Health System, Mobile, USA.

Thuy Phung (T)

Pathology and Laboratory Medicine, University of South Alabama College of Medicine, Mobile, USA.

Classifications MeSH