https://doi.org/10.4081/aamr.2019.79
Left paranasal hemophilic pseudotumor in a 5-year-old boy: A case report
Published: January 15, 2020
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All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Authors
Hemophilic pseudotumors are rare complications of hemophilia that are seen in 1-2% of patients commonly affecting patients with severe disease. Hemophilic pseudotumors occur as a result of recurrent poorly managed or untreated bleeding either in the soft tissue or bone. We report a 5-year-old boy with a previously undiagnosed hemophilia A who developed left paranasal swelling following a fall from a height. He was diagnosed with hemophilic pseudotumor and successfully managed conservatively with factor VIII replacement.
Faisal YS, Faizan YS, Shahid B. Hemophilicpseudotumors: Natural history and a case report of pseudotumor with femur fracture and swan-neck deformity. International Journal of Orthopaedics Sciences. 2016;2(1):10–4.
Panotopoulos J, Ay C, Trieb K, Funovics PT, Stockhammer V, Lang S, et al. Surgical treatment of the haemophilic pseudotumour: A single centre experience. 2012;(36):2157–62.
Gupta S, Mohapatra BB, Ghai S, Seith A, Kashyap R, Sharma R, et al. Haemophilic pseudotumour of the paranasal sinuses: management with radiotherapy and factor replacement therapy. Haemophilia.2001;(7):595–9.
Xue F, Sun C, Sui T, Zhang L, Jiang L, Yang R. HemophilicPseudotumor in Chinese Patients: A Retrospective Single-Centered Analysis of 14 Cases. Clinical and Applied Thrombosis/Hemostasis. 2011;279–82.
Gilbert MS. The hemophilicpseudotumor.ProgClinBiol Res. 1990;(324):257–62.
Park JS, Ryu KN. Hemophilicpseudotumor involving the musculoskeletal system: spectrum of radiologic findings. AJR Am J Roentgenol. 2004 Jul;183(1):55–61.
Cox DP, Solar A, Huang J, Chigurupati R. Pseudotumor of the Mandible as First Presentation of Hemophilia in a 2-Year-Old Male: A Case Report and Review of Jaw Pseudotumors of Hemophilia. Head and Neck Pathol. (5):226–32.
Mahmud A, Bashir Y, Taura MG, Adamu LH. Haemophilic Pseudotumor: A Rare Pathological Entity Involving 5th Metacarpal and Associated Tissues. Sch J App Med Sci. 2015;3(4B):1707–11.
How to Cite
Yuguda, S., Girei, A. I., Dachi, R. A., & Adamu, S. (2020). Left paranasal hemophilic pseudotumor in a 5-year-old boy: A case report. Annals of African Medical Research, 2(2). https://doi.org/10.4081/aamr.2019.79
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