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Radiographic findings in Waldenström's macroglobulinemia resembling fibrogenesis imperfecta ossium (FIO): a case
Narendranath Epperla1, Fergus E McKiernan, Charles V Kenney
1Department of Internal Medicine, Marshfield Clinic, 1000 N Oak Ave, Marshfield, WI, 54449, USA, enaren10@gmail.com.
Abstract:
A case of Waldenström's macroglobulinemia with radiographic features of fibrogenesis imperfecta ossium is presented. The case raises the possibility that these radiographic findings might be more common in Waldenström's macroglobulinemia than previously appreciated, and illustrates the need for bone biopsy to establish a definitive diagnosis of fibrogenesis imperfecta ossium.
Insights
This case study highlights a rare association between Waldenström's macroglobulinemia and fibrogenesis imperfecta ossium. Radiographic findings may be more common than previously thought, necessitating bone biopsy for diagnosis.
Area of Science:
- Hematology
- Radiology
- Pathology
Background:
- Waldenström's macroglobulinemia is a rare lymphoproliferative disorder.
- Fibrogenesis imperfecta ossium is a rare genetic bone disorder.
Observation:
- A patient presented with Waldenström's macroglobulinemia and radiographic findings suggestive of fibrogenesis imperfecta ossium.
Findings:
- The co-occurrence of these conditions was observed.
- Radiographic features of fibrogenesis imperfecta ossium may be underrecognized in Waldenström's macroglobulinemia.
Implications:
- This case suggests a potential link between the two conditions.
- Bone biopsy is crucial for definitive diagnosis of fibrogenesis imperfecta ossium in such cases.
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