A Rare Case of Subcutaneous Amyloidoma Associated with Localized Lymphoplasmacytic Lymphoma: Diagnostic Challenges and Treatment Considerations

Lisa Francesca Vivian; Lukas Marcelis; Eleonora Leoni; Yves De Bruecker; Helena Maes; Erwin Pierré; Florence M. Ballaux; Thomas Tousseyn

doi:10.12659/AJCR.940789

02 October 2023 : Case report Italy

A Rare Case of Subcutaneous Amyloidoma Associated with Localized Lymphoplasmacytic Lymphoma: Diagnostic Challenges and Treatment Considerations

Rare disease, Rare coexistence of disease or pathology

Lisa Francesca Vivian

^1ABDEF*, Lukas Marcelis

^23ABDE, Eleonora Leoni^4D, Yves De Bruecker^5BD, Helena Maes^6BD, Erwin Pierré^7BD, Florence M. Ballaux^7BD, Thomas Tousseyn

^23ABCDEFG

DOI: 10.12659/AJCR.940789

Am J Case Rep 2023; 24:e940789

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Background Case Report Discussion Conclusions References:

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Figure 3. Ultrasound study of the elbow lesion at 1-month follow-up after the first excision. A first amorphous, band-shaped hypoechogenic zone without vascularization can be recognized, and interpreted as postoperative changes (arrow). Next to it, the clinically relevant, palpable subcutaneous nodule corresponds to a hypoechogenic soft-tissue mass measuring 1.4×0.8 cm (asterisk) and showing focal vascularization in Doppler study, thus warranting further investigation and removal for histopathological evaluation (A: B-mode; B: Doppler study).

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A Rare Case of Subcutaneous Amyloidoma Associated with Localized Lymphoplasmacytic Lymphoma: Diagnostic Challenges and Treatment Considerations

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