Spontaneous psoas hematoma following posterior lumbar fusion surgery: a mini literature review
Background Spontaneous psoas hematoma is a very rare clinical entity, and the pathogenesis and pathologic mechanisms of spontaneous psoas hematoma remain unclear, thus, it is of great value to explore. Case presentation We encountered a patient who developed femoral nerve paralysis due to psoas musc...
Saved in:
Published in | BMC musculoskeletal disorders Vol. 26; no. 1; pp. 244 - 6 |
---|---|
Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BioMed Central
12.03.2025
BioMed Central Ltd BMC |
Subjects | |
Online Access | Get full text |
ISSN | 1471-2474 1471-2474 |
DOI | 10.1186/s12891-025-08455-9 |
Cover
Summary: | Background
Spontaneous psoas hematoma is a very rare clinical entity, and the pathogenesis and pathologic mechanisms of spontaneous psoas hematoma remain unclear, thus, it is of great value to explore.
Case presentation
We encountered a patient who developed femoral nerve paralysis due to psoas muscle hematoma following posterior lumbar fusion surgery. A 69-year-old female with lumbar spinal canal stenosis underwent posterior lumbar fusion at the L3-4 and L4-5 levels. On the 7th postoperative day, the patient complained of severe abdominal pain along with right limb pain and weakness. A computed tomography image showed a large acute psoas muscle hematoma on the right side. After conservative treatment, the psoas hematoma was resolved and the patient’s femoral nerve paralysis gradually recovered.
Conclusions
Spontaneous psoas hematoma is a rare and extremely dangerous complication after lumbar spine surgery. For high - risk patients who have taken anticoagulants before the operation, we must be vigilant against the occurrence of this complication. |
---|---|
Bibliography: | ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Review-5 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 1471-2474 1471-2474 |
DOI: | 10.1186/s12891-025-08455-9 |