MerlinDX Artikel D48.1
https://www.askep3s.org/91ab860383/artikel/D48.1
Artikel Klinis ICD-10: D48.1

D48.1: Neoplasma dengan Perilaku Tidak Pasti atau Tidak Diketahui pada Jaringan Ikat dan Jaringan Lunak Lainnya

1 menit baca Terverifikasi: 2026-08-05
Bagikan:

📚 Daftar Pustaka (APA 7)

[1]
World Health Organization. (2020). WHO Classification of Tumours of Soft Tissue and Bone. 5th Edition. Lyon: IARC Press.
[2]
Goldblum, J.R., Folpe, A.L., & Weiss, S.W. (2020). Enzinger and Weiss's Soft Tissue Tumors. 7th Edition. Philadelphia: Elsevier.
[3]
Kasper, B., et al. (2022). 'European consensus approach for desmoid tumors: a joint European consensus initiative.' Annals of Oncology, 33(5), 456-467.
[4]
Nishida, Y., et al. (2021). 'Management of desmoid-type fibromatosis: a survey of Japanese experts.' International Journal of Clinical Oncology, 26(2), 345-354.
[5]
Skubitz, K.M. (2017). 'Biology and treatment of aggressive fibromatosis or desmoid tumor.' Mayo Clinic Proceedings, 92(6), 947-964.
[6]
WHO. (2019). International Classification of Diseases for Mortality and Morbidity Statistics. 10th Revision. Geneva: World Health Organization.
[7]
Fiore, M., et al. (2019). 'Desmoid-type fibromatosis: a chronic disease?' Annals of Oncology, 30(8), 1232-1233.
[8]
Penel, N., et al. (2021). 'Management of desmoid tumours: a nationwide survey of labelled reference networks in France.' European Journal of Cancer, 148, 1-10.
[9]
Gounder, M.M., et al. (2018). 'Sorafenib for Advanced and Refractory Desmoid Tumors.' New England Journal of Medicine, 379(25), 2417-2428.
[10]
Cates, J.M.M., & Stricker, T.P. (2019). 'Soft Tissue Tumors of Uncertain Differentiation.' Surgical Pathology Clinics, 12(1), 165-199.

🔗 Konten Terkait: D48.1

Pathway: D48.1 Neoplasma Jaringan Lunak & SDKI