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Segmental schwannomatosis: characteristics in 12 patients.
Alaidarous, Abdulqader; Parfait, Beatrice; Ferkal, Salah; Cohen, Joëlle; Wolkenstein, Pierre; Mazereeuw-Hautier, Juliette.
Afiliação
  • Alaidarous A; Service de Dermatologie, Hôpital Larrey, CHU de Toulouse, Toulouse, France. abdulqader.alaidarous@gmail.com.
  • Parfait B; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Ferkal S; UMR INSERM 1016 Institut Cochin & Université Paris Descartes, Sorbonne Paris Cité, Paris, France.
  • Cohen J; Service de Dermatologie, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris, Creteil, France.
  • Wolkenstein P; Service de Génétique et Biologie Moléculaires, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Mazereeuw-Hautier J; Service de Dermatologie, Hôpital Henri Mondor, Assistance Publique-Hôpitaux de Paris, Creteil, France.
Orphanet J Rare Dis ; 14(1): 207, 2019 08 22.
Article em En | MEDLINE | ID: mdl-31438995
ABSTRACT

BACKGROUND:

Segmental schwannomatosis is characterized by multiple schwannomas affecting one-limb or less than 5 contiguous segments of spine. Its characteristics are not well described in the literature. Our objective was to better describe the demographic and clinical characteristics of this condition.

METHODS:

This was a retrospective, bi-center study conducted in two French expert centers for neurofibromatosis and schwannomatosis. The clinical, radiographic, pathological and molecular aspects were extracted from patients' clinical records.

RESULTS:

Twelve patients with segmental schwannomatosis were identified. Eight were female and 4 were male. The median age at initial symptom was 29 years (range 6-60 years) and the median age at diagnosis was 34.5 years (range 13-65 years). Pain was the initial symptom for the majority of patients (7 of 12). The number of tumors was variable with six patients having more than 10 tumors. Peripheral distribution was seen in all patients. Quality of life could be impaired (median Dermatology Life Quality Index score was 4.5 (range 2-13). The median duration of follow up was 3 years (range 1-26). Chronic pain was the main complication (9 of 12 patients). Surgical intervention to control chronic pain was performed for 9 patients of whom 5 experienced recurrence of tumors. Molecular investigations revealed heterozygous LZTR1 variants in 3 of 9 patients.

CONCLUSION:

Segmental schwannomatosis is a rare condition that may start early in life and often remains undiagnosed for many years. Pain is the main symptom and consequently could impair the quality of life. Surgery seems to be effective, but recurrences are frequent. Some patients carried heterozygous LZTR1 variants. Further studies are needed to better understand this rare condition.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatoses / Dor Crônica / Neurilemoma Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Neurofibromatoses / Dor Crônica / Neurilemoma Idioma: En Ano de publicação: 2019 Tipo de documento: Article