Outcome of thoracic primitive neuroectodermal tumors in pediatrics : A single-institution experience / Mona Ahmed Moustafa Elsaudi ; Supervised Hossam Eldeen Ahmed Abdelmonem , Ahmed Mohammed Kamel , Ibrahim Abdelrahman Ibrahim
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- دراسة استرجاعية لنتائج علاج الأطفال المرضى بأورام الصدر للغدد العصبية البدائية بالمعهد القومى للأورام . مصر [Added title page title]
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قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.19.05.M.Sc.2021.Mo.O (Browse shelf(Opens below)) | Not for loan | 01010110083940000 | ||
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مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.19.05.M.Sc.2021.Mo.O (Browse shelf(Opens below)) | 83940.CD | Not for loan | 01020110083940000 |
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Thesis (M.Sc.) - Cairo University - National Cancer Institute - Department of Pediatric (Oncology)
Background:Primitive neuroectodermal tumors (PNETs) are malignant and aggressive 2small round cells3 neoplasms that arise from the primitive nerve cells of the central nervous system (central PNETs), but at times, they can affect any peripheral nerve (peripheral PNETs) in the neck, chest wall, retroperitoneum, pelvis, and extremities (Khmou et al., 2016). In 1979, Askin et al. described for the first time, 20 cases of children and adolescents affected by PNETs of the thoracopulmonary region.Since then,PNETs developed within the soft tissue of the thoracopulmonary region are referred to as 2Askin{u2019}s tumors3 [AT] (Triarico et al., 2018).In addition to this, Askin{u2019}s tumors occur typically in children and adolescents and they belong to the Ewing{u2019}s sarcoma (EW) family because of their histological, immunohistochemically, cytogenetic, and phenotypic similarities (Parikh M et al., 2011).Because of the rarity of this neoplasm, the approach to Askin{u2019}s tumors is complex and it may require a multidisciplinary management (Devi LP et al., 2015)
Issued also as CD
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