Literature DB >> 23172474

Rapidly progressive thyroid mass: amyloid goiter.

Metin Ibrahimov1, Mehmet Yilmaz, Erkan Kilic, Ferit Akil, Resul Rasidov, Emin Karaman.   

Abstract

Amyloidosis is a disease of unknown etiology characterized by the accumulation of an amorphous proteinaceous material in various organs and tissues of the body. Amyloid goiter is an exceedingly rare pathologic condition due to massive amyloid infiltration of the thyroid tissue. Amyloid goiter occurs in association with both primary and secondary systemic amyloidosis, more commonly in the latter. Preoperatively, it simulates a multinodular goiter, and surgical intervention is often necessary to establish a diagnosis and to relieve compressive symptoms of a neck mass. We present the case of an 85-year-old female patient who presented with a rapidly enlarging goiter. Histologic examination confirmed amyloid goiter.

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Year:  2012        PMID: 23172474     DOI: 10.1097/SCS.0b013e31825cef34

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  3 in total

1.  Amyloid goiter - A rare case report and literature review.

Authors:  Eisa Lari; Waleed Burhamah; Ali Lari; Salman Alsafran; Ali Ismail
Journal:  Ann Med Surg (Lond)       Date:  2020-08-13

2.  A rare case of primary thyroid amyloidosis.

Authors:  M A Cannizzaro; S Lo Bianco; W Saliba; S D'Errico; F Pennetti Pennella; G Buttafuoco; D Provenzano; G Magro
Journal:  Int J Surg Case Rep       Date:  2018-10-25

Review 3.  Nodular goiter with amyloid deposition in an elderly patient: fine-needle cytology diagnosis and review of the literature.

Authors:  Vincenzo Di Crescenzo; Alfredo Garzi; Fara Petruzziello; Mariapia Cinelli; Lucio Catalano; Pio Zeppa; Mario Vitale
Journal:  BMC Surg       Date:  2013-10-08       Impact factor: 2.102

  3 in total

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