Tracheobronchial amyloidosis-a series of two cases.

Kavita V, Palak D Raiyani, Sunil S Vyas
Author Information
  1. Kavita V: Assistant Professor, Department of General Pathology, Christian Medical College , Vellore, India .
  2. Palak D Raiyani: Assistant Professor, Department of General Pathology, Christian Medical College , Vellore, India .
  3. Sunil S Vyas: Assistant Professor, Department of Pulmonary Medicine, Christian Medical College , Vellore, India .

Abstract

Amyloidosis is a rare disorder characterised by accumulation of insoluble fibrillar proteins in extracellular space. Respiratory amyloidosis presents as two tracheobronchial forms (local and diffuse) and two parenchymal forms (nodular and diffuse), of which diffuse tracheobronchial amyloidosis is the least common. We herein present two cases of tracheobronchial amyloidosis.

Keywords

References

  1. Histopathology. 1998 Apr;32(4):356-61 [PMID: 9602333]
  2. Eur J Radiol. 2002 Oct;44(1):37-9 [PMID: 12350409]
  3. Am J Surg Pathol. 1987 Dec;11(12):989-95 [PMID: 3120605]
  4. Thorax. 1999 May;54(5):444-51 [PMID: 10212113]
  5. J Med Case Rep. 2012 Jan 30;6:40 [PMID: 22289269]
  6. Respir Med. 1997 Sep;91(8):499-502 [PMID: 9338055]

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