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Updated: Jan 29, 2026

An Organotypic High Throughput System for Characterization of Drug Sensitivity of Primary Multiple Myeloma Cells
Published on: July 15, 2015
Plasma Cell Myeloma Masquerading as Scleromyxedema
Varun Victor1, Rashmi Maria Margareat1
1Department of General Medicine, St. John's Medical College, Bengaluru, Karnataka, India.
Scleromyxedema, a rare skin condition, was effectively treated in a multiple myeloma patient using bortezomib, thalidomide, and dexamethasone. This combination therapy led to complete resolution of the patient's skin lesions.
Area of Science:
- Dermatology
- Hematology
- Oncology
Background:
- Scleromyxedema is a rare, progressive cutaneous mucinosis of unknown cause, affecting men and women equally.
- It is frequently associated with monoclonal gammopathy, complicating treatment options.
- Established treatments like steroids, IVIg, stem cell transplant, and melphalan show limited efficacy.
Observation:
- A case of scleromyxedema was reported in a patient who was subsequently diagnosed with multiple myeloma.
- The patient presented with characteristic skin lesions of scleromyxedema.
Findings:
- The patient received six cycles of a specific chemotherapy regimen: bortezomib, thalidomide, and dexamethasone.
- This treatment resulted in complete resolution of all scleromyxedema skin lesions.
Implications:
- This case highlights a successful therapeutic approach for scleromyxedema, particularly when co-occurring with multiple myeloma.
- The bortezomib, thalidomide, and dexamethasone combination offers a promising treatment option for refractory scleromyxedema.
- Further research into this regimen's efficacy and safety in scleromyxedema patients is warranted.
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