Thin-Needle Biopsy in the Diagnosis of Thyroid Disease

1962 ◽  
Vol 58 (5) ◽  
pp. 321-336 ◽  
Author(s):  
J. Einhorn ◽  
S. Franzen
1962 ◽  
Vol Original Series, Volume 58 (5) ◽  
pp. 321-336
Author(s):  
J. Einhorn ◽  
S. Franzen

1976 ◽  
Vol 69 (6special) ◽  
pp. 860-865
Author(s):  
Kunihiko NAGAHARA ◽  
Hitosi IWAI ◽  
Junji KONISHI ◽  
Kiyoyuki TAKAHASHI

2017 ◽  
Vol 99 (3) ◽  
pp. 233-236 ◽  
Author(s):  
E Aysan ◽  
T Kiran ◽  
UO Idiz ◽  
B Guler ◽  
H Akbulut ◽  
...  

INTRODUCTION Non-diagnostic results of fine needle aspiration biopsy (FNAB) remain an important limitation of this technqiue. The aim of our study was to evaluate the results of core needle biopsy (CNB) of thyroid nodules and its effectiveness in non-diagnostic FNAB cases. METHODS CNBs were performed in 1,000 patients (154 male, 846 female; mean age: 50.2 years, range: 18–86 years) with a spring loaded 20G needle. Of these, 143 had initially had FNABs that were insufficient for evaluation. The CNB reports were reviewed. Patients with suspicious or malignant CNB results underwent total thyroidectomy. RESULTS When considering all 1,000 CNBs, the non-diagnostic rate was 1.5% (15/1,000). However, when the first 100 cases were eliminated as a learning curve, this reduced to 0.9% (8/900). Of the 143 cases with initial FNABs that were non-diagnostic, 0.7% (1/143) were also non-diagnostic on CNB. Twelve patients underwent surgery because of malignant CNB reports and all of these cases were confirmed as malignant by the postoperative pathology specimen results (100% accuracy). There were no major complications although three self-limiting minor complications were observed. CONCLUSIONS CNB is a safe and accurate method. It is more diagnostic than FNAB for nodular thyroid disease.


Author(s):  
P.K. Simons

Glycogenosis is defined as any condition in which the tissue concentration of glycogen is increased. There are currently ten recognized variants of glycogenosis that are heritable inborn errors of metabolism. The specific enzymatic defect in each of the variants is known or at least suspected. In all cases, the enzymatic defect prevents the proper metabolism or formation of the glycogen molecule. The clinical and histologic differences between the types of glycogenosis is important to a proper diagnosis after the presence of such a condition is realized. This study was initiated to examine the ultrastructure of the rare Type IV Glycogenosis (Amylopectinosis) of which there is very little morphologic characterization in the literature.Liver tissue was obtained by needle biopsy from a 12-month-old Oriental female who was originally admitted to the hospital after observation of poor development, loss of appetite, and hepatomegaly. The majority of the tissue was fixed for light microscopy in neutral buffered formalin and processed using routine and special staining procedures (reticulin, trichrome, iron, copper, PAS, PAS-diastase and PAS-pectinase.


1956 ◽  
Vol 30 (3) ◽  
pp. 373-381 ◽  
Author(s):  
Edward M. Schneider ◽  
Walter Joel ◽  
Mervin L. Clark
Keyword(s):  

1951 ◽  
Vol 18 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Herman Ulevitch ◽  
E.A. Gall ◽  
E.L. Abernathy ◽  
Leon Schiff
Keyword(s):  

2007 ◽  
Vol 177 (4S) ◽  
pp. 127-128
Author(s):  
Michael Muntener ◽  
Jonathan I. Epstein ◽  
David J. Hernandez ◽  
Mark L. Gonzalgo ◽  
Leslie A. Mangold ◽  
...  

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