Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2022 Jan;95(1):92-96.
doi: 10.15386/mpr-1751. Epub 2022 Jan 31.

Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis

Affiliations
Case Reports

Epithelioid angiosarcoma of the masseter muscle: a rare clinicopathological diagnosis

Anitya Srivastava et al. Med Pharm Rep. 2022 Jan.

Abstract

Epithelioid angiosarcoma (EA) is a subtype of angiosarcoma which is a rare tumor of endothelial origin. Here, we report a case of 15-year-old boy who presented with soft tissue mass lesion in the parotid region mimicking as a benign parotid tumor. Cytology was suggestive of inflammatory swelling. Patient underwent superficial parotidectomy along with the wide excision of the swelling. On histopathology, it was diagnosed as EA. To the best of our knowledge this is the first case report of epithelioid angiosarcoma of the masseter.

Keywords: chemotherapy; epithelioid angiosarcoma; masseter muscle; parotid; radiotherapy.

PubMed Disclaimer

Figures

Figure 1
Figure 1
(a) Markings showing the mass and the modified Blair’s incision in the preauricular region. (b): CT scan showing hypodense lesion occupying the left masseter muscle. (c) Intraoperative picture showing facial nerve and its branches after superficial parotidectomy with small nodular mass in the masseter muscle.
Figure 2
Figure 2
(a,b) Tumor cells are arranged in sheets with interspersed foci of necrosis, congestion, haemorrhage, cystic degeneration and large blood vessels (H&E stain, 10× and 20× respectively). (c) Epithelioid to plump spindle shaped tumor cells having large, moderately pleomorphic round to ovoid nuclei, coarse chromatin, moderate to abundant eosinophilic cytoplasm with few mitotic figures and rich network of small caliber blood vessels are noted (H&E stain, 40×). (d) Immunohistochemistry shows nuclear positivity for FLI-1.

Similar articles

Cited by

References

    1. Hart J, Mandavilli S. Epithelioid angiosarcoma: a brief diagnostic review and differential diagnosis. Arch Pathol Lab Med. 2011;135:268–272. - PubMed
    1. Weiss SW, Ishak KG, Dail DH, Sweet DE, Enzinger FM. Epithelioid hemangioendothelioma and related lesions. Semin Diagn Pathol. 1986;3:259–287. - PubMed
    1. Mullins B, Hackman T. Angiosarcoma of the Head and Neck. Int Arch Otorhinolaryngol. 2015;19:191–195. - PMC - PubMed
    1. Wu J, Li X, Liu X. Epithelioid angiosarcoma: a clinicopathological study of 16 Chinese cases. Int J Clin Exp Pathol. 2015;8:3901–3909. - PMC - PubMed
    1. Ayadi L, Khabir A. Pediatric angiosarcoma of soft tissue: a rare clinicopathologic entity. Arch Pathol Lab Med. 2010;134:481–485. - PubMed

Publication types

LinkOut - more resources