Journals / Çağdaş Cerrahi Dergisi / 1998 / Cilt: 12 - Sayı: 1

Amlyloid goiter ( A case report )

Amiloid guatr ( Olgu sunumu )

Pages
57–59
Publication Date
2022-11-05
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Prognosis is poor, because of the underlying disease and systemic deposits of amyloid.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Amyloid goiter is a rare clinic entity, usually with systemic secondary amyloidosis.
📊
Key Findings & Data:In a 33 years old patient, under hemodilaysis programme for end-stage chronic renal failure, we had determined amyloid goiter ofAA type.
💡
Conclusion & Impact:Prognosis is poor, because of the underlying disease and systemic deposits of amyloid.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Amyloid goiter is a rare clinic entity, usually with systemic secondary amyloidosis. In a 33 years old patient, under hemodilaysis programme for end-stage chronic renal failure, we had determined amyloid goiter ofAA type. Preoperative diagnosis of amyloid goiter is difficult but ultrasonography and fine needle, aspiration biopsy is helpful. In treatment, bilateral subtotal thyroidectomy is adequate. Prognosis is poor, because of the underlying disease and systemic deposits of amyloid.

🔖

Cite This Article

GÖKSOY, E., KAPAN, M., AKSOY, F., EREK, E. (2022). Amlyloid goiter ( A case report ). Çağdaş Cerrahi Dergisi, Cilt: 12 - Sayı: 1, 57–59. https://ajindex.com/articles/649499