Bone angiosarcoma in the humerus of a pediatric patient, a whole diagnostic challenge: case report
DOI:
https://doi.org/10.17533/udea.iatreia.118Keywords:
bone and bones, child, hemangiosarcomaAbstract
Angiosarcoma of the bone is a rare, aggressive and poor-prognosis malignancy, that is unusual in children. This entity preferentially affects the tubular bones, and can present as a solitary or multicentric lesion. We present the case of a 7-year-old girl, without medical surgical history, who onsulted to the National Cancer Institute - Colombia, for presenting a tumor lesion that compromised the entire humerus, destroying it and deforming the arm. To guide the diagnosis of the lesion, a detailed histopathological study and immunohistochemical markers were performed, which suggested a alignant vascular neoplasm. Due to the extensive tumor involvement, the only therapeutic option was scapulothoracic disarticulation of the limb, followed by adjuvant management with a hemotherapy protocol. During the chemotherapy cycles, the patient presented metastatic lesions in the lung, which were resected. At the moment, she is without tumor lesions and under close follow-up.
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(1) Bernstock JD, Shafaat O, Hardigan A, Fox BM, Moore LS, Chagoya G, et al. Angiosarcoma of the Temporal Bone: Case Report and Review of the Literature. World Neurosurg. 2019 Oct;130:351–7. DOI 10.1016/j.wneu.2019.07.107.
(2) van IJzendoorn DGP, Bovée JVMG. Vascular Tumors of Bone: The Evolvement of a Classification Based on Molecular Developments. Surg Pathol Clin. 2017 Sep;10(3):621–35.
(3) WHO Classification of Tumours Editorial Board. Soft Tissue and Bone Tumours. 5th. ed. Lyon (France): Lyon International Agency for Research on Cancer; 2020.
(4) Gaballah AH, Jensen CT, Palmquist S, Pickhardt PJ, Duran A, Broering G, et al. Angiosarcoma: clinical and imaging features from head to toe. Br J Radiol. 2017 Jul;90(1075):20170039.
(5) Wenger DE, Wold LE. Malignant vascular lesions of bone: radiologic and pathologic features. Skeletal Radiol. 2000;29(11):619–31. DOI 10.1007/s002560000261.
(6) Akhavan Tafti M, Jafari N, Zare J, Jalal Jafari M. A Case of Bone Angiosarcoma. Iran J Pathol. 2016;11(5):465-8.
(7) Wang J, Zhao M, Huang J, Ang L, Zheng L. Primary epithelioid angiosarcoma of right hip joint: A case report and literature review. Medicine (Baltimore). 2018 Apr;97(15):e0307–e0307. DOI 10.1097/MD.0000000000010307.
(8) Czerniak B, Dorfman HD. Dorfman and Czerniak’s bone tumours. Philadelphia: Elsevier; 2016.
(9) Pülhorn H, Elliot T, Clark J, Gonzalvo A. Case report: Angiosarcoma of the cervical spine. J Clin Neurosci. 2017 Nov;45:129–31. DOI 10.1016/j.jocn.2017.07.018.
(10) Eilebrecht K. Pediatric bone and soft tissue sarcomas. Berlin: Springer; 2010.
(11) PDQ Pediatric Treatment Editorial Board. Childhood Vascular Tumors Treatment (PDQ®): Patient Version. 2019 Aug 29. In: PDQ Cancer Information Summaries. Bethesda (MD): National Cancer Institute (US); 2002.
(12) Dunlap JB, Magenis RE, Davis C, Himoe E, Mansoor A. Cytogenetic analysis of a primary bone angiosarcoma. Cancer Genet Cytogenet. 2009 Oct;194(1):1–3. DOI 10.1016/j.cancergencyto.2009.04.008.
(13) Verbeke SLJ, Bertoni F, Bacchini P, Sciot R, Fletcher CDM, Kroon HM, et al. Distinct histological features characterize primary angiosarcoma of bone. Histopathology. 2011 Jan;58(2):254–64. DOI 10.1111/j.1365-2559.2011.03750.x.
(14) Sakamoto A, Takahashi Y, Oda Y, Iwamoto Y. Aggressive clinical course of epithelioid angiosarcoma in the femur: a case report. World J Surg Oncol. 2014 Sep 11;12:281. DOI 10.1186/1477-7819-12-281.
(15) Verbeke SLJ, de Jong D, Bertoni F, Sciot R, Antonescu CR, Szuhai K, et al. Array CGH analysis identifies two distinct subgroups of primary angiosarcoma of bone. Genes Chromosomes Cancer. 2015 Feb;54(2):72–81. DOI 10.1002/gcc.22219.
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