Literature DB >> 24351625

Combined pulmonary involvement in hereditary lysozyme amyloidosis with associated pulmonary sarcoidosis: a case report.

Cormac McCarthy1, Alexander P Deegan, John F Garvey, Timothy J McDonnell.   

Abstract

Sarcoidosis is a multisystem inflammatory disorder of unknown cause which can affect any organ system. Autosomal dominant lysozyme amyloidosis is a very rare form of hereditary amyloidosis. The Arg64 variant is extraordinarily rare with each family showing a particular pattern of organ involvement, however while Sicca syndrome, gastrointestinal involvement and renal failure are common, lymph node involvement is very rare. In this case report we describe the first reported case of sarcoidosis in association with hereditary lysozyme amyloidosis.

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Year:  2013        PMID: 24351625

Source DB:  PubMed          Journal:  Sarcoidosis Vasc Diffuse Lung Dis        ISSN: 1124-0490            Impact factor:   0.670


  1 in total

Review 1.  Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.

Authors:  Audrey Benyamine; Fanny Bernard-Guervilly; Céline Tummino; Nicolas Macagno; Laurent Daniel; Sophie Valleix; Brigitte Granel
Journal:  Clin Rheumatol       Date:  2017-09-30       Impact factor: 2.980

  1 in total

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