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Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report

RATIONALE: Complex regional pain syndrome (CRPS) is a painful condition classified as type I or II depending on the absence or presence of nerve injury, respectively. Injury to the lateral dorsal cutaneous nerve (LDCN), a branch of the sural nerve, is a rare occurrence observed after a sprain or pro...

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Autores principales: Kim, Tae-Hoon, Jo, Geun-Yeol, Kim, Wanil, Do, Hwan-Kwon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663875/
https://www.ncbi.nlm.nih.gov/pubmed/34889267
http://dx.doi.org/10.1097/MD.0000000000028108
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author Kim, Tae-Hoon
Jo, Geun-Yeol
Kim, Wanil
Do, Hwan-Kwon
author_facet Kim, Tae-Hoon
Jo, Geun-Yeol
Kim, Wanil
Do, Hwan-Kwon
author_sort Kim, Tae-Hoon
collection PubMed
description RATIONALE: Complex regional pain syndrome (CRPS) is a painful condition classified as type I or II depending on the absence or presence of nerve injury, respectively. Injury to the lateral dorsal cutaneous nerve (LDCN), a branch of the sural nerve, is a rare occurrence observed after a sprain or procedures conducted on the lateral side of the ankle. PATIENT CONCERNS: A 38-year-old female, who had undergone prolotherapy for a sprain in the lateral side of the left ankle 3 months ago, presented with persistent causalgia and dysesthesia around the injection site. DIAGNOSIS: An electrodiagnostic study was conducted, which confirmed that the patient had peripheral neuropathy of the left LDCN. Considering the digital infrared thermal imaging and three-phase bone scan findings and the clinical presentation, the condition was diagnosed as CRPS type II due to iatrogenic LDCN injury according to the Budapest diagnostic criteria for CRPS. INTERVENTIONS: The patient was treated with steroid pulse therapy, physical therapy, and transcutaneous electrical nerve stimulation, as well as nonsteroidal anti-inflammatory drugs, pregabalin, and tricyclic antidepressants. OUTCOMES: After 1 month of treatment, allodynia of the left foot persisted, but the pain reduced from 6 points to 3 points on the numeric rating scale. Partial recovery of amplitude and conduction velocity was confirmed in the follow-up electrodiagnostic study. LESSONS: LDCN injury should be considered in patients who complain of persistent lateral ankle and foot paresthesia or pain after sprain or procedures performed on the lateral side of the ankle. Early diagnosis and treatment can lead to a good prognosis when the LDCN injury has progressed to CRPS.
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spelling pubmed-86638752021-12-13 Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report Kim, Tae-Hoon Jo, Geun-Yeol Kim, Wanil Do, Hwan-Kwon Medicine (Baltimore) 6300 RATIONALE: Complex regional pain syndrome (CRPS) is a painful condition classified as type I or II depending on the absence or presence of nerve injury, respectively. Injury to the lateral dorsal cutaneous nerve (LDCN), a branch of the sural nerve, is a rare occurrence observed after a sprain or procedures conducted on the lateral side of the ankle. PATIENT CONCERNS: A 38-year-old female, who had undergone prolotherapy for a sprain in the lateral side of the left ankle 3 months ago, presented with persistent causalgia and dysesthesia around the injection site. DIAGNOSIS: An electrodiagnostic study was conducted, which confirmed that the patient had peripheral neuropathy of the left LDCN. Considering the digital infrared thermal imaging and three-phase bone scan findings and the clinical presentation, the condition was diagnosed as CRPS type II due to iatrogenic LDCN injury according to the Budapest diagnostic criteria for CRPS. INTERVENTIONS: The patient was treated with steroid pulse therapy, physical therapy, and transcutaneous electrical nerve stimulation, as well as nonsteroidal anti-inflammatory drugs, pregabalin, and tricyclic antidepressants. OUTCOMES: After 1 month of treatment, allodynia of the left foot persisted, but the pain reduced from 6 points to 3 points on the numeric rating scale. Partial recovery of amplitude and conduction velocity was confirmed in the follow-up electrodiagnostic study. LESSONS: LDCN injury should be considered in patients who complain of persistent lateral ankle and foot paresthesia or pain after sprain or procedures performed on the lateral side of the ankle. Early diagnosis and treatment can lead to a good prognosis when the LDCN injury has progressed to CRPS. Lippincott Williams & Wilkins 2021-12-10 /pmc/articles/PMC8663875/ /pubmed/34889267 http://dx.doi.org/10.1097/MD.0000000000028108 Text en Copyright © 2021 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0 (https://creativecommons.org/licenses/by/4.0/)
spellingShingle 6300
Kim, Tae-Hoon
Jo, Geun-Yeol
Kim, Wanil
Do, Hwan-Kwon
Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title_full Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title_fullStr Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title_full_unstemmed Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title_short Complex regional pain syndrome type II caused by iatrogenic lateral dorsal cutaneous nerve injury: A case report
title_sort complex regional pain syndrome type ii caused by iatrogenic lateral dorsal cutaneous nerve injury: a case report
topic 6300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8663875/
https://www.ncbi.nlm.nih.gov/pubmed/34889267
http://dx.doi.org/10.1097/MD.0000000000028108
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