2022, Number 01
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MediSan 2022; 26 (01)
Hereditary factors and syndromes of genetic predisposition related to sarcomas of soft parts
Puig GCJ, Puig CJC, Castro BL
Language: Spanish
References: 31
Page: 190-203
PDF size: 1208.08 Kb.
ABSTRACT
The sarcomas of soft parts are malignancies that originate in the connective tissue, starting from the embryonic mesenchyme. Taking into account the existence of new and constant changes in the nature of these tumors, a review of the most recent publications was carried out to deepen in the genetic disorders, the predisposing syndromes and its relationship with sarcomas. It was concluded that the records that describe the identification of these syndromes are still very few as main link in the development of sarcomas.
REFERENCES
López Pousa A. Tratamiento de los sarcomas de partes blandas. Barcelona: Hospital de la Santa Creu i Sant Paul. Sociedad Española de Oncología Médica;2016 [citado 22/01/2021]. Disponible en: https://seom.org/seomcms/images/stories/recursos/sociosyprofs/comunicaciones/tenerife/ix_tenerife043.pdf
Galy Bernadoy, Garrel R . Head and neck soft-tissue sarcoma in adults. Eur Ann Otorhinolaryngol Head Neck Dis. 2016 [citado 22/01/2021];133(1):37-42. Disponible en: https://pubmed.ncbi.nlm.nih.gov/26403655/
Kazuhiro T, Toshifumi O. New TNM classification (AJCC eighth edition) of bone and soft tissue sarcomas: JCOG Bone and Soft Tissue Tumor Study Group. Jpn J Clin Oncol. 2019 [citado 22/01/2021]; 49(2). Disponible en: https://academic.oup.com/jjco/article/49/2/103/5179391
Ray Coquard I, Serre D, Reichardt P, Martín Broto J, Bauer S. Options for treating different soft tissue sarcoma subtypes. Future Oncol. 2018 [citado 22/01/2021]; 14(10):25-49. Disponible en: https://pubmed.ncbi.nlm.nih.gov/29768052/
Ventura Martínez N, Cebreros Rosas D, Miragall Alba L, Ruiz Gutierrez JP, Puglia-Santos V. Sarcoma de Ewing extraóseo en cabeza y cuello: revisión de la literatura a propósito de un caso. Rev Esp Cir Oral Maxilo Fac. 2017 [citado 22/01/2021]; 39(2):105-12. Disponible en: https://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-05582017000200105
Arranz J, Patricia F, Díaz A. Guía oncosur de sarcomas de partes blandas. Madrid: Fundación OncoSur; 2017 [citado 22/01/2021]. Disponible en: https://congresos.grupoaran.com/guia-oncosur-sarcomas/files/assets/basic-html/page-1.html
Siegel R, Miller K, Jemal A. Cancer statistics, 2016. CA Cancer J Clin. 2016 [citado 22/01/2021];66(1):7-30. Disponible en: https://pubmed.ncbi.nlm.nih.gov/26742998/
Chávez M, Ziegler G, Cotrina J, Galarreta J, Cruz M de la, Mantilla R. Current situation of soft tissue sarcomas: Registry of a Latin American Cancer Institute. Cir Española. 2019 [citado 22/01/2021];97(4):203-12. Disponible en: https://www.elsevier.es/en-revista-cirugia-espanola-english-edition--436-articulo-current-situation-soft-tissue-sarcomas-S2173507719300742
Mahajan A, Mohanty S, Ghosh S, Aadithya B, Urs A, Sunita G. Sarcomatoid carcinoma of the oral cavity: a diagnostic dilemma. Case Reports in Dentistry. 2017 [citado 22/01/2021] Article ID 7495695. Disponible en: https://www.hindawi.com/journals/crid/2017/7495695/
Pérez Huitrón MA, Domínguez Castillo PM. El retinoblastoma: un tumor de ojo frecuente en la infancia. Rev. Fac. Med. (Méx.). 2019 [citado 22/01/2021]; 62(4). Disponible en: https://downloads.hindawi.com/journals/crid/2017/7495695.pdf
Dimaras H, Corson TW. Retinoblastoma, the visible CNS tumor: a review. J Neurosci Res. 2019 [citado 22/01/2021];97(1):29-44. https://pubmed.ncbi.nlm.nih.gov/29314142/
Czarnecka AM, Synoradzki K, Firlej W, Bartnik E, Sobczuk P, Fiedorowicz M, et al. Molecular biology of osteosarcoma. Cancers (Basel). 2020 [citado 22/01/2021]; 12(8):2130. Disponible en: https://pubmed.ncbi.nlm.nih.gov/32751922/
Miranda Alcalde B, Villa Alcázar M, Martínez Romera I, López Ibor B. Importancia del síndrome de Li-Fraumeni, un síndrome genético de predisposición al cáncer. Arch Argent Pediatr. 2021 [citado 22/01/2021];119(1):e11-e7. Disponible en: https://www.sap.org.ar/docs/publicaciones/archivosarg/2021/v119n1a16.pdf
Rodríguez Jiménez P, Reolid A, Chicharro P, Navarro R, Llamas Velasco M, Aragüés M. Treatment and prognosis of angiosarcoma: experience with 12 patients and review of new therapeutic lines. Med Cutan Iber Lat Am. 2017 [citado 22/01/2021]; 45(2): 112-18. Disponible en: https://www.medigraphic.com/pdfs/cutanea/mc-2017/mc172e.pdf
Sánchez Forero RA, Jaramillo LF, Ramírez J. Angiosarcoma cutáneo en la región nasal tratado con radioterapia: reporte de caso. Univ. Med. Colombia. 2018 [citado 22/01/2021];59(3). Disponible en: http://www.scielo.org.co/pdf/unmed/v59n3/0041-9095-unmed-59-03-00094.pdf
Camejo N, Castillo C, Richter L, Massia MN, Artagaveytia N, Neffa F, et al. Síndrome de Li Fraumeni: análisis clínico de un caso y revisión de la literatura Rev. Urug. Med. Int. 2018 [citado 22/01/2021];3:20-6. Disponible en: http://www.scielo.edu.uy/scielo.php?script=sci_arttext&pid=S2393-67972018000300020
Ossa CA, Molina G, Cock Rada AM. Síndrome de Li-Fraumeni. Biomédica. 2016 [citado 22/01/2021];36:182. Disponible en: http://www.scielo.org.co/pdf/bio/v36n2/v36n2a04.pdf
Miranda Alcaldea B, Villa Alcázara M, Martínez Romera I, López Ibo B. The importance of Li-Fraumeni syndrome, a hereditary cancer predisposition disorder. Arch Argent Pediatr. 2021 [citado 22/01/2021];119(1):11-7. Disponible en: https://pubmed.ncbi.nlm.nih.gov/33458985/
Adil A, Koritala T, Singh A. Neurofibromatosis Type 1. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021 [citado 22/01/2021]. Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK459358/
Hameed M, Mandelker D. Tumor syndromes predisposing to osteosarcoma. Adv Anat Pathol. 2018 [citado 22/01/2021];25(4):217-22. Disponible en: https://pubmed.ncbi.nlm.nih.gov/29668499/
Duat Rodríguez A. Neurofibromatosis tipo 1. Pediatr Integral. 2020 [citado 22/01/2021]; 24(6): 334-41. Disponible en: https://www.pediatriaintegral.es/publicacion-2020-09/neurofibromatosis-tipo-1/
Martinez AP, Fritchie KJ. Update on Peripheral Nerve Sheath Tumors. Surg Pathol Clin. 2019 [citado 22/01/2021];12(1):1-19. Disponible en: https://pubmed.ncbi.nlm.nih.gov/30709438/
Charifa A, Jamil RT, Zhang X. Gardner Syndrome. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2021 [citado 22/01/2021]. Disponible en: https://pubmed.ncbi.nlm.nih.gov/29493967/
Maita F, Mamani Vidal CA, Morales Reinaga LA, Arnés Terrazas R, Sánchez Soria Galvarro K. Complejo esclerosis tuberosa: diagnóstico, manejo pre y posnatal: reporte de un caso clínico. Gac Med Bol. 2017 [citado 22/01/2021]; 40(1): 41-5. Disponible en: http://www.scielo.org.bo/scielo.php?script=sci_arttext&pid=S1012-29662017000100009
Gómez Cerdas MT, Vargas Morales JA. Esclerosis tuberosa. Rev Méd Sinerg. 2019 [citado 22/01/2021];4(3):21. Disponible en: https://revistamedicasinergia.com/index.php/rms/article/view/182
Ballesteros Zárate ZY, Pardo Heredia AE, Martínez Martínez JS. Tuberous Sclerosis Complex, Main Characteristics and Cutaneous Manifestations. A Pediatric case. Dermatol Cosmética Méd Quir. 2019 [citado 22/01/2021];17(3):179-83. Disponible en: https://www.medigraphic.com/pdfs/cosmetica/dcm-2019/dcm193e.pdf
Hafsi W, Badri T. Poikiloderma Congenitale. In: StatPearls. Treasure Island (FL): StatPearls Publishing; 2020 [citado 22/01/2021]. Disponible en: https://www.ncbi.nlm.nih.gov/books/NBK526123/
Schaefer IM, Hornick JL. Diagnostic Immunohistochemistry for Soft Tissue and Bone Tumors: An Update. Adv Anat Pathol. 2018 [citado 22/01/2021];25(6):400-12. Disponible en: https://pubmed.ncbi.nlm.nih.gov/30134255/
Mukherjee S, Sinha D, Bhattacharya S, Srinivasan K, Abdisalaam S, Asaithamby A. Werner Syndrome protein and DNA replication. Int J Mol Sci. 2018 [citado 22/01/2021];19(11):3442. Disponible en: https://pubmed.ncbi.nlm.nih.gov/30400178/
De Renty C, Ellis NA. Bloom's syndrome: why not premature aging? A comparison of the BLM and WRN helicases. Ageing Res Rev. 2017 [citado 22/01/2021];33:36-51. Disponible en: https://pubmed.ncbi.nlm.nih.gov/27238185/
Acosta Aragón M, Sierra Zúñiga MF, Sotelo Muñoz NF. Síndrome de Werner a propósito de un caso probable. Medicina y laboratorio. 2017 [citado 22/01/2021];23(9-10):485-92. Disponible en: https://medicinaylaboratorio.com/index.php/myl/article/view/27