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Malignant psoas syndrome associated with gynecological malignancy: Three case reports and a review of the literature
- Publication Year :
- 2018
- Publisher :
- D.A. Spandidos, 2018.
-
Abstract
- Malignant psoas syndrome (MPS) is a rare and unique cancer-associated syndrome caused by the malignant involvement of the psoas major muscle, and is characterized by ipsilateral lumbosacral plexopathy and painful hip flexion. The pain in MPS is often distressing and intractable, and there is no established effective treatment approach. Herein, the present study reports on three cases of MPS associated with gynecological malignancies, wherein symptom improvement was observed following chemotherapy or radiotherapy. Among 39 cases documented in the literature, female genital tract malignancies were the most frequent causes of MPS; however, the condition may be under-diagnosed, owing to the lack of general recognition. Considering the development of recent high-precision radiation therapy, palliative radiotherapy may serve an important role in the management of MPS. For physicians treating gynecological cancers, early detection of MPS is clinically important as this may allow patients to receive possible therapies and improve their quality of life in end-stage cancer. Further prospective studies should be performed to evaluate effective therapeutic approaches for MPS.
- Subjects :
- Cancer Research
medicine.medical_specialty
Chemotherapy
congenital, hereditary, and neonatal diseases and abnormalities
business.industry
medicine.medical_treatment
Cancer
nutritional and metabolic diseases
Articles
medicine.disease
030218 nuclear medicine & medical imaging
Radiation therapy
03 medical and health sciences
0302 clinical medicine
Oncology
Quality of life
Palliative radiotherapy
030220 oncology & carcinogenesis
Internal medicine
Psoas major muscle
medicine
Psoas Syndrome
Prospective cohort study
business
skin and connective tissue diseases
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....392e1edac8b156baf3a2818398c196f8