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Erschienen in: Skeletal Radiology 10/2008

01.10.2008 | Scientific Article

MR findings in patients with disabling musculocutaneous chronic graft-versus-host disease

verfasst von: M. Horger, A. Boss, W. Bethge, C. Faul, G. Fierlbeck, A. Bornemann, C. D. Claussen, W. Vogel

Erschienen in: Skeletal Radiology | Ausgabe 10/2008

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Abstract

Objective

To describe musculocutaneous MR-findings responsible for disability in chronic graft-versus-host disease (cGVHD) after allogeneic hematopoietic cell transplantation (HCT).

Material and methods

Between June 2005 and February 2008, we performed whole-body musculoskeletal magnetic resonance imaging (MRI; n = 12) or regional MRI (n = 4) in 16 consecutive patients presenting with disabling sclerodermatous cGVHD (e.g., skin edema, fixed deep dermal sclerosis, joint contractures, painful muscular contractures, or myalgia).

Results

In all patients, MRI showed musculocutaneous abnormalities reflecting different degrees of inflammation and collagen tissue involvement of the skin (n = 10), subcutaneous fat tissue (n = 13), muscle fasciae (n = 16), subfascial muscular septae (n = 6), or findings compatible with myositis (n = 3). The most frequently involved muscle fasciae comprised those of the vastus lateralis muscle (n = 12), biceps femoris muscle (n = 11), gastrocnemius medialis muscle (n = 8), serratus anterior muscle, and latissimus dorsi muscle (each, n = 5). Increased signal of involved tissues on STIR-images and fat-saturated postgadolinium T1-weighted images represented the most frequent MR-signal abnormalities.

Conclusion

MR imaging of musculocutaneous cGVHD allows accurate evaluation including assessment of deep tissue infiltration and assists in the differential diagnosis.
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Metadaten
Titel
MR findings in patients with disabling musculocutaneous chronic graft-versus-host disease
verfasst von
M. Horger
A. Boss
W. Bethge
C. Faul
G. Fierlbeck
A. Bornemann
C. D. Claussen
W. Vogel
Publikationsdatum
01.10.2008
Verlag
Springer-Verlag
Erschienen in
Skeletal Radiology / Ausgabe 10/2008
Print ISSN: 0364-2348
Elektronische ISSN: 1432-2161
DOI
https://doi.org/10.1007/s00256-008-0535-3

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