Italian journal of pediatrics · 2016
Congenital Glioblastoma multiforme and eruptive disseminated Spitz nevi.
Клинический случайСтатьяОбзорНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Mandel Victor Desmond, Persechino Flavia, Berardi Alberto, Ponti Giovanni, Ciardo Silvana, Rossi Cecilia, Pellacani Giovanni, Farnetani Francesca
Аннотация
BACKGROUND: Glioblastoma multiforme (GBM) is the deadliest malignant primary brain tumor in adults. GBM develops primarily in the cerebral hemispheres but can develop in other parts of the central nervous system. Its congenital variant is a very rare disease with few cases described in literature.
CASE PRESENTATION: We describe the case of a patient with congenital GBM who developed eruptive disseminated Spitz nevi (EDSN) after chemotherapy. Few cases of EDSN have been described in literature and this rare clinical variant, which occurs predominantly in adults, is characterized by multiple Spitz nevi in the trunk, buttocks, elbows and knees. There is no satisfactory treatment for EDSN and the best therapeutic choice is considered the clinical observation of melanocytic lesions.
CONCLUSION: We recommend a close follow-up of these patients with clinical observation, dermoscopy and reflectance confocal microscopy (RCM). However, we suggest a surgical excision of the lesions suspected of being malignant.
CASE PRESENTATION: We describe the case of a patient with congenital GBM who developed eruptive disseminated Spitz nevi (EDSN) after chemotherapy. Few cases of EDSN have been described in literature and this rare clinical variant, which occurs predominantly in adults, is characterized by multiple Spitz nevi in the trunk, buttocks, elbows and knees. There is no satisfactory treatment for EDSN and the best therapeutic choice is considered the clinical observation of melanocytic lesions.
CONCLUSION: We recommend a close follow-up of these patients with clinical observation, dermoscopy and reflectance confocal microscopy (RCM). However, we suggest a surgical excision of the lesions suspected of being malignant.
Предметные рубрики MeSH
Antineoplastic Combined Chemotherapy ProtocolsApgar ScoreBrain NeoplasmsChemotherapy, AdjuvantCombined Modality TherapyDermoscopyFollow-Up StudiesGestational AgeGlioblastomaHumansInfant, NewbornMaleNeurosurgical ProceduresNevus, Epithelioid and Spindle CellRare DiseasesRisk AssessmentSkin NeoplasmsTreatment Outcome