Atypical cellular neurothekeoma: a case report with a novel NF1 mutation

Atypical cellular neurothekeoma is a rare benign soft-tissue tumour that usually arises in the head and neck region, shoulder girdles, and proximal extremities, predominantly in young women. This dermal neoplasm is under-reported in the literature and is not uncommonly misdiagnosed as a malignant tumour due to its worrisome histologic characteristics. Currently, the diagnosis of cellular neurothekeoma relies on a panel of non-specific immunohistochemical markers and its etiopathogenesis is unknown.Herein, we present the case of an atypical cellular neurothekeoma in the arm of a 49-year-old woman, describing its microscopic features and immunohistochemical profile. Additionally, we present a novel heterozygous predicted inactivating NF1 mutation, not previously reported, which was identified using high-throughput molecular techniques. Such finding might provide insights into the pathogenesis of neurothekeoma, potentially contributing to future refinements in diagnosis, which would enable more precise identification of this neoplasm.

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Publication Details

Journal
Diagnostic Pathology
Published
2024-11-22
DOI
https://doi.org/10.1186/s13000-024-01578-y
Citations
3
Primary Topic
Neurofibromatosis and Schwannoma Cases
Type
article
Field-Weighted Citation Impact
1.11
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article

Atypical cellular neurothekeoma: a case report with a novel NF1 mutation

Marina Pacheco, Valli de la Guardia, Ana I. Porcell, Edgardo Castro-Pérez et al.
3 citations
Diagnostic Pathology
Neurofibromatosis and Schwannoma Cases
1.11
article

Atypical cellular neurothekeoma: a case report with a novel NF1 mutation

Marina Pacheco, Valli de la Guardia, Ana I. Porcell, Edgardo Castro-Pérez, Sara González de Tena-Dávila
article en
3 citations

Abstract

Atypical cellular neurothekeoma is a rare benign soft-tissue tumour that usually arises in the head and neck region, shoulder girdles, and proximal extremities, predominantly in young women. This dermal neoplasm is under-reported in the literature and is not uncommonly misdiagnosed as a malignant tumour due to its worrisome histologic characteristics. Currently, the diagnosis of cellular neurothekeoma relies on a panel of non-specific immunohistochemical markers and its etiopathogenesis is unknown.Herein, we present the case of an atypical cellular neurothekeoma in the arm of a 49-year-old woman, describing its microscopic features and immunohistochemical profile. Additionally, we present a novel heterozygous predicted inactivating NF1 mutation, not previously reported, which was identified using high-throughput molecular techniques. Such finding might provide insights into the pathogenesis of neurothekeoma, potentially contributing to future refinements in diagnosis, which would enable more precise identification of this neoplasm.

Diagnostic PathologyVol. 19(1)
Universidad de Panamá (PA), Universidad de Salamanca (ES), National Oncologic Institute (PA), Secretaría Nacional de Ciencia, Tecnología e Innovación (PA), Instituto de Investigaciones Científicas y Servicios de Alta Tecnología (PA), Hospital Metropolitano (EC), City of Knowledge (PA)
Openalex Percentile: Top 20%
Neurofibromatosis and Schwannoma Cases
1.11
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Atypical cellular neurothekeoma: a case report with a novel NF1 mutation — Marina Pacheco, Valli de la Guardia, et al. · Diagnostic Pathology (2024) | TGRS Research Map | TGRS