Primary osseous amyloidoma - Report of two cases with review of the literature

Journal Title: Journal of Modern Human Pathology - Year 2018, Vol 3, Issue 3

Abstract

Amyloidoma, also known as tumoral amyloidosis, is a rare localized subset of amyloidosis without systemic involvement. Amyloid becomes aggregated in the extracellular matrix ofvarious tissues such as the respiratory, urinary, central nervous systems, heart, salivary glands, breast and orbital tissue. Very few cases of osseous amyloidosis have been reported in the literature, especially in the absence of systemic amyloidosis or dialysis. The two cases that follow describe such lesions which were identified in the bone.

Authors and Affiliations

Clarissa Smith, Da Zhang, Larry Hoover, Howard Rosenthal

Keywords

Related Articles

Roles of HMGA proteins in cancer: Expression, pathways, and redundancies

The expression of the High Mobility Group A (HMGA) proteins, their participation in cancer signalling pathways, and their redundant functions have been reviewed in seven types of cancer: breast, colorectal, prostate, lun...

Inflammatory myofibroblastic tumor of the uterus that might STUMP you: Report of a case with clinicopathological and immunohistochemical findings

Inflammatory myofibroblastic tumor is an under-recognized locally aggressive tumor that has rarely been described in the uterus. We present a case in a 40-year-old patient with a large tumor mass in the posterior wall of...

Azathioprine induced Epstein-Barr virus positive mucocutaneous ulcer: A case report

Introduction: Epstein-Barr virus positive mucocutaneous ulcer (EBVMUC) is a rare, newly described provisional entity in the 2016 Update of World Health Organization classification of lymphoid neoplasms. The histomorpholo...

Spatiotemporal expression of matrix metalloproteinase-1 in progression of nonalcoholic steatohepatitis

Human matrix metalloproteinase-1 (MMP-1) has been shown to contribute to the regression of experimental liver fibrosis when ectopically expressed in rodents. It remains unknown whether the same mechanism exists in chroni...

Talc induced pulmonary granulomatosis: An under recognized complication in patients with cystic fibrosis

Talc induced pulmonary granulomatosis is a known pulmonary condition that is associated with intravenous drug exposure. Only one documented case of talc induced pulmonary granulomatosis in a patient with cystic fibrosis...

Download PDF file
  • EP ID EP530034
  • DOI 10.14312/2397-6845.2018-3
  • Views 46
  • Downloads 0

How To Cite

Clarissa Smith, Da Zhang, Larry Hoover, Howard Rosenthal (2018). Primary osseous amyloidoma - Report of two cases with review of the literature. Journal of Modern Human Pathology, 3(3), 7-11. https://europub.co.uk./articles/-A-530034