Bilateral multifocal lower extremity localized soft tissue amyloidomas: case report with ultrasonographic characterization

Tanner C. Clark, Bart Kimbrell, Nicole Girard, Barry Hansford

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Amyloidosis may be acquired or hereditary and consists of multiple disease processes characterized by the abnormal deposition of extracellular fibrillary protein aggregates. The presentation of amyloidosis is varied, ranging from an isolated, focal deposition to systemic disease. While systemic involvement is common, a rare entity known as amyloidoma or tumor amyloidosis may also occur. The 75-year-old female in this case presented with slowly growing multifocal bilateral lower extremity masses and was ultimately diagnosed with localized amyloidomas in the absence of chronic illness or systemic disease. This case report includes a description of the sonographic features of localized extremity amyloidoma that, to the best of our knowledge, have not yet been described in the literature. Awareness of the sonographic features, and this unique presentation of multifocal soft tissue extremity amyloidomas will allow for this rare diagnosis to be included in a limited differential diagnosis.

Original languageEnglish (US)
Pages (from-to)1783-1789
Number of pages7
JournalSkeletal Radiology
Volume46
Issue number12
DOIs
StatePublished - Dec 1 2017
Externally publishedYes

Fingerprint

Amyloidosis
Lower Extremity
Extremities
Differential Diagnosis
Chronic Disease
Neoplasms

Keywords

  • Amyloidoma
  • Localized amyloidosis
  • Tumor amyloidoma
  • Ultrasound

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging

Cite this

Bilateral multifocal lower extremity localized soft tissue amyloidomas : case report with ultrasonographic characterization. / Clark, Tanner C.; Kimbrell, Bart; Girard, Nicole; Hansford, Barry.

In: Skeletal Radiology, Vol. 46, No. 12, 01.12.2017, p. 1783-1789.

Research output: Contribution to journalArticle

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