Abstract
DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1 gene. The risk to present a neoplasm before the age of 10 years is 5.3 and 31.5% before the age of 60. DICER1 variants have been associated with a syndrome involving familial pleuropulmonary blastoma (PPB), a rare malignant tumor of the lung, which occurs primarily in children under the age of 6 years and represents the most common life-threatening manifestation of DICER1 syndrome. Type I, II, III, and Ir (type I regressed) PPB are reported with a 5-year overall survival ranging from 53 to 100% (for type Ir). DICER1 gene should be screened in all patients with PPB and considered in other tumors mainly in thyroid neoplasms (multinodular goiter, thyroid cancer, adenomas), ovarian tumors (Sertoli-Leydig cell tumor, sarcoma, and gynandroblastoma), and cystic nephroma. A prompt identification of this syndrome is necessary to plan a correct follow-up and screening during lifetime.
Highlights
DICER1 syndrome is a cancer-predisposing disorder caused by pathogenic variants in the DICER1 gene (OMIM 606241), which are known to confer a lifetime risks for a variety of neoplastic and dysplastic lesions [1].Germline DICER1 variants have been detected in individuals affected with familial pleuropulmonary blastoma (PPB) [2,3,4,5], a rare malignant tumor of the lung, which occurs primarily in children under the age of 6 years [6]
DICER1 syndrome occurs in children and young adults and its clinical presentation may include, beyond PPB, cystic nephroma, ovarian Sertoli-Leydig cell tumor (SLCT), DICER1 Syndrome and Cancer Predisposition multinodular goiter, cervix embryonal rhabdomyosarcoma, Wilms’ tumor, nasal chondromesenchymal hamartoma, ciliary body medulloepithelioma, differentiated thyroid carcinoma, pituitary blastoma, pineoblastoma, and sarcomas of different sites including, amongst others, the uterine cervix, kidney, and brain [8]
This paper aims to review the clinical and genetic features of DICER1 syndrome, with particular focus on the description of the different types of cancer reported in this syndrome, grouped by systems
Summary
DICER1 syndrome is a rare genetic condition predisposing to hereditary cancer and caused by variants in the DICER1 gene. The risk to present a neoplasm before the age of 10 years is 5.3 and 31.5% before the age of 60. DICER1 variants have been associated with a syndrome involving familial pleuropulmonary blastoma (PPB), a rare malignant tumor of the lung, which occurs primarily in children under the age of 6 years and represents the most common life-threatening manifestation of DICER1 syndrome. DICER1 gene should be screened in all patients with PPB and considered in other tumors mainly in thyroid neoplasms (multinodular goiter, thyroid cancer, adenomas), ovarian tumors (Sertoli-Leydig cell tumor, sarcoma, and gynandroblastoma), and cystic nephroma. A prompt identification of this syndrome is necessary to plan a correct follow-up and screening during lifetime
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