Kaposiform haemangioendothelioma of the spine associated with fixed hyperlordotic deformity and Kasabach–Merritt Syndrome: a case report and literature review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Radiology, Nuclear Medicine and imaging
Link
https://link.springer.com/content/pdf/10.1007/s00256-022-04152-z.pdf
Reference23 articles.
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2. Croteau SE, Liang MG, Kozakewich HP, et al. Kaposiform hemangioendothelioma: atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals. J Pediatr. 2013;162(1):142–7.
3. Schmid I, Klenk AK, Sparber-Sauer M, Koscielniak E, Maxwell R, Häberle B. Kaposiform hemangioendothelioma in children: a benign vascular tumor with multiple treatment options. World J Pediatr. 2018;14(4):322–9.
4. International Society for the Study of Vascular Anomalies. ISSVA classification of vascular anomalies ©2014. 2017. Available from: issva.org/classification
5. Niedt GW, Greco MA, Wieczorek R, Blanc WA, Knowles DM. Hemangioma with Kaposi’s sarcoma-like features: report of two cases. Pediatr Pathol. 1989;9(5):567–75.
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1. Kaposiform hemangioendothelioma presented with raynaud phenomenon: a case report;BMC Pediatrics;2023-11-17
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