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A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation

INTRODUCTION: Primary intraosseous arteriovenous malformations (AVMs) are rare and have only been occasionally reported. We herein report a histologically proven case of primary intraosseous AVM in the distal humerus which mimicked an osteomyelitis on radiography. CASE REPORT: A 27-year-old male pre...

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Autores principales: Aravindasamy, M, Harshavardhan, J K Giriraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276614/
https://www.ncbi.nlm.nih.gov/pubmed/32548002
http://dx.doi.org/10.13107/jocr.2250-0685.1526
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author Aravindasamy, M
Harshavardhan, J K Giriraj
author_facet Aravindasamy, M
Harshavardhan, J K Giriraj
author_sort Aravindasamy, M
collection PubMed
description INTRODUCTION: Primary intraosseous arteriovenous malformations (AVMs) are rare and have only been occasionally reported. We herein report a histologically proven case of primary intraosseous AVM in the distal humerus which mimicked an osteomyelitis on radiography. CASE REPORT: A 27-year-old male presented with complaints of the right elbow pain and stiffness for the past 3 years. He had initially taken treatment at an outside hospital where he was suspected to have right distal humerus osteomyelitis and underwent curettage and biopsy in June 2017. He presented to us in August 2018 with persistent pain even following the first surgery. Repeat radiographs and computed tomography of the right elbow showed features of osteolytic lesion involving the right lateral humeral condyle just adjacent to olecranon fossa (Fig. 1 and 2). Through posterior triceps, splitting approach para-olecranon lesion was resected by intralesional method (burring), and vancomycin-impregnated calcium sulfate (Stimulan) beads were packed in the defect as infection was suspected (Fig. 3). Clinical improvement and restoration of full range of elbow motion were observed on follow-up. Biopsy report surprisingly suggested arteriovenous malformation. CONCLUSION: Osteolytic lesion was localized in the lateral margin of the olecranon fossa (Fig. 2a and b). To reach the lesion during surgery was a major challenge as localization of the lesion was missed out by the previous surgery. The occurrence of such a condition is rare and it may take even years to correctly diagnose the disease.
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spelling pubmed-72766142020-06-15 A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation Aravindasamy, M Harshavardhan, J K Giriraj J Orthop Case Rep Case Report INTRODUCTION: Primary intraosseous arteriovenous malformations (AVMs) are rare and have only been occasionally reported. We herein report a histologically proven case of primary intraosseous AVM in the distal humerus which mimicked an osteomyelitis on radiography. CASE REPORT: A 27-year-old male presented with complaints of the right elbow pain and stiffness for the past 3 years. He had initially taken treatment at an outside hospital where he was suspected to have right distal humerus osteomyelitis and underwent curettage and biopsy in June 2017. He presented to us in August 2018 with persistent pain even following the first surgery. Repeat radiographs and computed tomography of the right elbow showed features of osteolytic lesion involving the right lateral humeral condyle just adjacent to olecranon fossa (Fig. 1 and 2). Through posterior triceps, splitting approach para-olecranon lesion was resected by intralesional method (burring), and vancomycin-impregnated calcium sulfate (Stimulan) beads were packed in the defect as infection was suspected (Fig. 3). Clinical improvement and restoration of full range of elbow motion were observed on follow-up. Biopsy report surprisingly suggested arteriovenous malformation. CONCLUSION: Osteolytic lesion was localized in the lateral margin of the olecranon fossa (Fig. 2a and b). To reach the lesion during surgery was a major challenge as localization of the lesion was missed out by the previous surgery. The occurrence of such a condition is rare and it may take even years to correctly diagnose the disease. Indian Orthopaedic Research Group 2019 /pmc/articles/PMC7276614/ /pubmed/32548002 http://dx.doi.org/10.13107/jocr.2250-0685.1526 Text en Copyright: © Indian Orthopaedic Research Group http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Aravindasamy, M
Harshavardhan, J K Giriraj
A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title_full A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title_fullStr A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title_full_unstemmed A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title_short A Rare Case of Distal Humerus Intraosseous Arteriovenous Malformation
title_sort rare case of distal humerus intraosseous arteriovenous malformation
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7276614/
https://www.ncbi.nlm.nih.gov/pubmed/32548002
http://dx.doi.org/10.13107/jocr.2250-0685.1526
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