دورية أكاديمية

Primary Cutaneous Leiomyosarcoma Arising in a Patient With Li-Fraumeni Syndrome: A Neoplasm With Unusual Histopathologic Features and Loss of Heterozygosity at TP53 Gene

التفاصيل البيبلوغرافية
العنوان: Primary Cutaneous Leiomyosarcoma Arising in a Patient With Li-Fraumeni Syndrome: A Neoplasm With Unusual Histopathologic Features and Loss of Heterozygosity at TP53 Gene
المؤلفون: Sabater Marco, Vicente, Ferrando Roca, Francisco, Morera Faet, Arturo, García García, José Ángel, Bosch, Sandra B., López Guerrero, José A.
المصدر: https://journals.lww.com/amjdermatopathology/fulltext/2018/03000/primary_cutaneous_leiomyosarcoma_arising_in_a.17.aspxTest.
سنة النشر: 2018
المجموعة: RIUCV - Universidad Católica de Valencia San Vicente Mártir
مصطلحات موضوعية: Li-Fraumeni syndrome (LFS), Breast cancer, Cutaneous, 3201.01 Oncología
الوصف: Li-Fraumeni syndrome (LFS) is an inherited cancer predisposition syndrome characterized by sarcomas in children and young adults, early-onset breast cancer, brain tumors, adrenal cortical carcinoma, and leukemia.1 In patients with this syndrome, several cutaneous neoplasias have been described such as multiple primary cutaneous melanomas,2 atypical fibrous histiocytoma,3 sebaceous carcinoma,4 infantile cutaneous rhabdomyosarcoma,5 and atypical fibroxanthoma.6 We report here the first cutaneous pilar-type leiomyosarcoma (LMS) arising in a patient with classic LFS. This tumor showed a plexiform growth pattern and similar areas to a symplastic pilar leiomyoma. Tumor analysis by Next-Generation Sequencing detected loss of heterozygosity (LOH) at TP53 gene. ; Medicina
نوع الوثيقة: article in journal/newspaper
اللغة: English
تدمد: 0193-1091
1533-0311
العلاقة: http://hdl.handle.net/20.500.12466/3409Test
الإتاحة: https://doi.org/20.500.12466/3409Test
https://hdl.handle.net/20.500.12466/3409Test
حقوق: Attribution-NonCommercial-NoDerivatives 4.0 Internacional ; http://creativecommons.org/licenses/by-nc-nd/4.0Test/ ; openAccess
رقم الانضمام: edsbas.2D8D3E12
قاعدة البيانات: BASE