Early Genetic Diagnosis of Neurofibromatosis Type 2 From Skin Plaque Plexiform Schwannomas in Childhood


Por: Castellanos, E, Plana, A, Carrato, C, Carrio, M, Rosas, I, Amilibia, E, Roca-Ribas, F, Hostalot, C, Castillo, A, Ros, A, Quer, A, Becerra, JL, Salvador, H, Lazaro, C, Blanco, I, Serra, E and Bielsa, I

Publicada: 1 mar 2018
Resumen:
IMPORTANCE Neurofibromatosis type 2 (NF2) is a devastating genetic condition characterized by the development of multiple tumors of the nervous system. An early diagnosis of individuals with NF2 would facilitate treatment and reduction of disease impact because most severe effects of the disease do not usually develop before adolescence. Little attention has traditionally been paid to dermatological signs in NF2. However, skin plaques are commonly seen in patients with NF2, normally appearing either at birth or early childhood, providing an opportunity for early NF2 detection and testing. OBJECTIVE To determine the clinical utility of skin plaque identification and characterization in children for reaching an early diagnosis of patients with NF2 and to evaluate their molecular pathogenesis and their use in the genetic diagnostics of NF2. DESIGN, SETTING AND PARTICIPANTS Diagnostic test study by the histological and genetic characterization of skin plaques from patients with NF2. Patients were 7 individuals with NE2 or clinical suspicion of NF2 treated at the Spanish Reference Center on Phakomatoses. MAIN OUTCOMES AND MEASURES Histological evaluation of all skin plaques was performed. Fresh skin plaques were cultured to obtain Schwann cells and the NF2 gene was genetically analyzed. For all 7 patients, NF2 clinical history was reviewed. RESULTS In all 7 patients (4 male and 3 female), all skin plaques analyzed were histologically characterized as plexiform schwannomas. Genetic analysis of primary Schwann cell cultures derived from them allowed the identification of a constitutional and a somatic NF2 mutation. Genetic testing allowed the early diagnosis of NF2 in a child only exhibiting the presence of skin plaques. Most of the patients with NF2 analyzed had an early presentation of skin plaques and a severe NF2 phenotype. CONCLUSIONS AND RELEVANCE This work emphasizes the clinical utility of a careful dermatological inspection and the correct identification of skin plaques in children for an early diagnosis of NF2. We show for the first time that Schwann cells derived from skin plaque plexiform schwannomas bear the double inactivation of the NF2 gene and thus constitute an excellent source of tissue for genetic testing, especially in the context of mosaicism.

Filiaciones:
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 Germans Trias & Pujol Res Inst IGTP, Hereditary Canc Grp IGTP CIBERONC, Program Predict & Personalized Med Canc PMPPC, Can Ruti Campus, Barcelona, Spain

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 Germans Trias & Pujol Hosp HUGTiP, Dept Dermatol, Can Ruti Campus, Barcelona, Spain

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 HUGTIP, Dept Pathol, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

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 Germans Trias & Pujol Res Inst IGTP, Hereditary Canc Grp IGTP CIBERONC, Program Predict & Personalized Med Canc PMPPC, Can Ruti Campus, Barcelona, Spain

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 Germans Trias & Pujol Res Inst IGTP, Hereditary Canc Grp IGTP CIBERONC, Program Predict & Personalized Med Canc PMPPC, Can Ruti Campus, Barcelona, Spain

Amilibia, E:
 HUGTiP, Dept Otorhinolaryngol, Can Ruti Campus, Barcelona, Spain

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 HUGTiP, Dept Otorhinolaryngol, Can Ruti Campus, Barcelona, Spain

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 HUGTiP, Dept Neurosurg, Can Ruti Campus, Barcelona, Spain

Castillo, A:
 HUGTiP, Clin Genet & Genet Counseling Program, Can Ruti Campus, Barcelona, Spain

Ros, A:
 HUGTiP, Clin Genet & Genet Counseling Program, Can Ruti Campus, Barcelona, Spain

Quer, A:
 HUGTIP, Dept Pathol, Barcelona, Spain

 Univ Autonoma Barcelona, Barcelona, Spain

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 HUGTiP, Dept Neurol, Can Ruti Campus, Barcelona, Spain

Salvador, H:
 Hosp St Joan de Deu Esplugues, Pediat Oncol Unit, Barcelona, Spain

Lazaro, C:
 Catalan Inst Oncol ICO IDIBELL CIBERONC, Hereditary Canc Program, Barcelona, Spain

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 HUGTiP, Clin Genet & Genet Counseling Program, Can Ruti Campus, Barcelona, Spain

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 Germans Trias & Pujol Res Inst IGTP, Hereditary Canc Grp IGTP CIBERONC, Program Predict & Personalized Med Canc PMPPC, Can Ruti Campus, Barcelona, Spain

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 Germans Trias & Pujol Hosp HUGTiP, Dept Dermatol, Can Ruti Campus, Barcelona, Spain
ISSN: 21686084





JAMA Dermatology
Editorial
American Medical Association, 330 N WABASH AVE, STE 39300, CHICAGO, IL 60611-5885 USA, Estados Unidos America
Tipo de documento: Article
Volumen: 154 Número: 3
Páginas: 341-346
WOS Id: 000427475000019
ID de PubMed: 29322178
imagen Green Published

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