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Intradural lumbar disc herniation of L2–L3: A case report and literature review
BACKGROUND: Intradural lumbar disc herniation (ILDH), especially upper lumbar intradural disc herniation, is a rare type of lumbar disc herniation (LDH). However, it may have severe and complex symptoms, causing serious impact on the patients. Additionally, it is difficult to be diagnosed with limit...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880181/ https://www.ncbi.nlm.nih.gov/pubmed/36713657 http://dx.doi.org/10.3389/fsurg.2022.1047974 |
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author | Chen, Xipeng Cheng, Yuanpei Wu, Han |
author_facet | Chen, Xipeng Cheng, Yuanpei Wu, Han |
author_sort | Chen, Xipeng |
collection | PubMed |
description | BACKGROUND: Intradural lumbar disc herniation (ILDH), especially upper lumbar intradural disc herniation, is a rare type of lumbar disc herniation (LDH). However, it may have severe and complex symptoms, causing serious impact on the patients. Additionally, it is difficult to be diagnosed with limited experience. Few studies on L2–L3 ILDH have been reported in the literature. This study presents such a case and reviews the incidence, etiology, symptoms, diagnosis and treatment of this disease, so as to provide guidance and experience for clinicians. CASE PRESENTATION: A 27-year-old male patient had a one-month history of severe lower back pain and left lower extremity weakness after lumbar sprain. He could not walk due to progressive symptoms. Physical examination revealed that straight leg raising and femoral nerve stretch tests on the left side were positive. Magnetic resonance imaging of lumbar showed an intradural disc protruding into the ventral dural sac at the L2–L3 level. He was diagnosed ILDH of L2–L3, finally. An urgent operation was performed to remove the intradural disc fragment. The patient's symptoms improved significantly, postoperatively. After eight months of follow-up, he returned to normal life with only slight lower back pain. CONCLUSIONS: ILDH at the L2–L3 level is an extremely rare type of LDH. Its diagnosis often requires a combination of symptom, physical examination, and imaging examination due to no typical symptoms or imaging features. A detailed preoperative plan including the definition of the position, calcification, migration, and adhesion of intradural intervertebral discs to decrease the risk of surgery, prevent the occurrence of complications, and promote postoperative prognosis of patients. |
format | Online Article Text |
id | pubmed-9880181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98801812023-01-28 Intradural lumbar disc herniation of L2–L3: A case report and literature review Chen, Xipeng Cheng, Yuanpei Wu, Han Front Surg Surgery BACKGROUND: Intradural lumbar disc herniation (ILDH), especially upper lumbar intradural disc herniation, is a rare type of lumbar disc herniation (LDH). However, it may have severe and complex symptoms, causing serious impact on the patients. Additionally, it is difficult to be diagnosed with limited experience. Few studies on L2–L3 ILDH have been reported in the literature. This study presents such a case and reviews the incidence, etiology, symptoms, diagnosis and treatment of this disease, so as to provide guidance and experience for clinicians. CASE PRESENTATION: A 27-year-old male patient had a one-month history of severe lower back pain and left lower extremity weakness after lumbar sprain. He could not walk due to progressive symptoms. Physical examination revealed that straight leg raising and femoral nerve stretch tests on the left side were positive. Magnetic resonance imaging of lumbar showed an intradural disc protruding into the ventral dural sac at the L2–L3 level. He was diagnosed ILDH of L2–L3, finally. An urgent operation was performed to remove the intradural disc fragment. The patient's symptoms improved significantly, postoperatively. After eight months of follow-up, he returned to normal life with only slight lower back pain. CONCLUSIONS: ILDH at the L2–L3 level is an extremely rare type of LDH. Its diagnosis often requires a combination of symptom, physical examination, and imaging examination due to no typical symptoms or imaging features. A detailed preoperative plan including the definition of the position, calcification, migration, and adhesion of intradural intervertebral discs to decrease the risk of surgery, prevent the occurrence of complications, and promote postoperative prognosis of patients. Frontiers Media S.A. 2023-01-13 /pmc/articles/PMC9880181/ /pubmed/36713657 http://dx.doi.org/10.3389/fsurg.2022.1047974 Text en © 2023 Chen, Cheng and Wu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Surgery Chen, Xipeng Cheng, Yuanpei Wu, Han Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title | Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title_full | Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title_fullStr | Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title_full_unstemmed | Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title_short | Intradural lumbar disc herniation of L2–L3: A case report and literature review |
title_sort | intradural lumbar disc herniation of l2–l3: a case report and literature review |
topic | Surgery |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9880181/ https://www.ncbi.nlm.nih.gov/pubmed/36713657 http://dx.doi.org/10.3389/fsurg.2022.1047974 |
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