prikaz prve stranice dokumenta Management of a rapidly enlarging supraclavicular mass of unknown aetiology
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Scientific paper - Case study
Management of a rapidly enlarging supraclavicular mass of unknown aetiology
BMJ Case Reports, 17 (2024), 2; e255774. https://doi.org/10.1136/bcr-2023-255774
Čukman, Mateo; Lužaić, Karla; Krstanović, Kristina; Stevanović, Siniša

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Čukman, M., Lužaić, K., Krstanović, K. & Stevanović, S. (2024). Management of a rapidly enlarging supraclavicular mass of unknown aetiology. BMJ Case Reports, 17. (2). doi: 10.1136/bcr-2023-255774

Čukman, Mateo, et al. "Management of a rapidly enlarging supraclavicular mass of unknown aetiology." BMJ Case Reports, vol. 17, no. 2, 2024. https://doi.org/10.1136/bcr-2023-255774

Čukman, Mateo, Karla Lužaić, Kristina Krstanović and Siniša Stevanović. "Management of a rapidly enlarging supraclavicular mass of unknown aetiology." BMJ Case Reports 17, no. 2 (2024). https://doi.org/10.1136/bcr-2023-255774

Čukman, M., et al. (2024) 'Management of a rapidly enlarging supraclavicular mass of unknown aetiology', BMJ Case Reports, 17(2). doi: 10.1136/bcr-2023-255774

Čukman M, Lužaić K, Krstanović K, Stevanović S. Management of a rapidly enlarging supraclavicular mass of unknown aetiology. BMJ Case Reports [Internet]. 2024 [cited 2024 October 31];17(2). doi: 10.1136/bcr-2023-255774

M. Čukman, K. Lužaić, K. Krstanović and S. Stevanović, "Management of a rapidly enlarging supraclavicular mass of unknown aetiology", BMJ Case Reports, vol. 17, no. 2, 2024. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:220:050536. [Accessed: 31 October 2024]

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Metadata
Title (english)Management of a rapidly enlarging supraclavicular mass of unknown aetiology
AuthorMateo Čukman
AuthorKarla Lužaić
AuthorKristina Krstanović
AuthorSiniša Stevanović
Author's institution(Sestre milosrdnice University Hospital Center)
Scientific / art field,
discipline and subdiscipline		BIOMEDICINE AND HEALTHCARE
Clinical Medical Sciences
Otorhinolaryngology
Abstract (english)
Intramuscular haemangiomas are benign tumours showing an extremely rare occurrence and making up less than 1% of all haemangiomas. The goal of this case report is to share our experience in treating a patient with an extremely rare intramuscular haemangioma, which occurred in the supraclavicular region VB level of the neck and extended towards the infraclavicular space, localised within and inferior to the trapezius muscle. The lesion was diagnosed by using multimodal imaging and a wide excision was performed with intraoperative feeding vessel ligation and a good postoperative result. The main difficulties regarding diagnosis and treatment include a lack of evidence-based guidelines, due to limited publications on this topic, the nature of the lesion frequently showing obscure anatomic localisation deep within muscles and unclear delineation, various anatomic origin requiring an individual treatment approach, inconclusive radiologic signs as well as non-specific symptoms.
Languageenglish
Publication typeScientific paper - Case study
Publication statusPublished
Peer reviewPeer review
Publication versionPublished version
Journal titleBMJ Case Reports
Numberingvol. 17, no. 2, e255774
e-ISSN1757-790X
DOIhttps://doi.org/10.1136/bcr-2023-255774
URN:NBNurn:nbn:hr:220:050536
Publication2024
Document URLhttps://casereports.bmj.com/content/17/2/e255774.long
Type of resourceText
Access conditionsInstitutional access
Terms of useLicence In copyright icon
Created on2024-10-18 09:46:19