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Osteoid Osteoma of the Distal Phalanx of Little Finger

INTRODUCTION: Although osteoid osteomas are relatively common lesion, sites such as distal phalanx are still rarely observed. These lesions present with characteristic nocturnal pain due to prostaglandins and may also be associated with clubbing. Diagnosis of these lesions at uncommon sites becomes...

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Autores principales: Ambulgekar, Rajesh K, Ghag, Niranjan Sunil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Indian Orthopaedic Research Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983399/
https://www.ncbi.nlm.nih.gov/pubmed/36873331
http://dx.doi.org/10.13107/jocr.2022.v12.i09.3330
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author Ambulgekar, Rajesh K
Ghag, Niranjan Sunil
author_facet Ambulgekar, Rajesh K
Ghag, Niranjan Sunil
author_sort Ambulgekar, Rajesh K
collection PubMed
description INTRODUCTION: Although osteoid osteomas are relatively common lesion, sites such as distal phalanx are still rarely observed. These lesions present with characteristic nocturnal pain due to prostaglandins and may also be associated with clubbing. Diagnosis of these lesions at uncommon sites becomes tricky and 85% are misdiagnosed. CASE REPORT: A 18-year-old patient presented with the left distal phalanx of little finger clubbing and nocturnal pain (visual analogue scale [VAS] score: 8). After clinical workup and investigation to rule out infective and other causes, the patient was posted for excision of the lesion with curettage. Post-surgery outcome showed reduced pain (2 months post-operative VAS score: 1) and good clinical results. CONCLUSION: Although osteoid osteoma of distal phalanx is a rare entity and difficult to diagnosed. Complete excision of lesion shows promising results both in terms of reduction of pain and functionally.
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spelling pubmed-99833992023-03-04 Osteoid Osteoma of the Distal Phalanx of Little Finger Ambulgekar, Rajesh K Ghag, Niranjan Sunil J Orthop Case Rep Case Report INTRODUCTION: Although osteoid osteomas are relatively common lesion, sites such as distal phalanx are still rarely observed. These lesions present with characteristic nocturnal pain due to prostaglandins and may also be associated with clubbing. Diagnosis of these lesions at uncommon sites becomes tricky and 85% are misdiagnosed. CASE REPORT: A 18-year-old patient presented with the left distal phalanx of little finger clubbing and nocturnal pain (visual analogue scale [VAS] score: 8). After clinical workup and investigation to rule out infective and other causes, the patient was posted for excision of the lesion with curettage. Post-surgery outcome showed reduced pain (2 months post-operative VAS score: 1) and good clinical results. CONCLUSION: Although osteoid osteoma of distal phalanx is a rare entity and difficult to diagnosed. Complete excision of lesion shows promising results both in terms of reduction of pain and functionally. Indian Orthopaedic Research Group 2022-09 2022-09 /pmc/articles/PMC9983399/ /pubmed/36873331 http://dx.doi.org/10.13107/jocr.2022.v12.i09.3330 Text en Copyright: © Indian Orthopaedic Research Group https://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
Ambulgekar, Rajesh K
Ghag, Niranjan Sunil
Osteoid Osteoma of the Distal Phalanx of Little Finger
title Osteoid Osteoma of the Distal Phalanx of Little Finger
title_full Osteoid Osteoma of the Distal Phalanx of Little Finger
title_fullStr Osteoid Osteoma of the Distal Phalanx of Little Finger
title_full_unstemmed Osteoid Osteoma of the Distal Phalanx of Little Finger
title_short Osteoid Osteoma of the Distal Phalanx of Little Finger
title_sort osteoid osteoma of the distal phalanx of little finger
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9983399/
https://www.ncbi.nlm.nih.gov/pubmed/36873331
http://dx.doi.org/10.13107/jocr.2022.v12.i09.3330
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