F. Fulciniti et al., Follicular variant of papillary carcinoma: Cytologic findings on FNAB samples - Experience with 16 cases, DIAGN CYTOP, 25(2), 2001, pp. 86-93
Between January 1, 1992 and December 31, 1997, a cytopathological diagnosis
of follicular variant of papillary thyroid carcinoma (FVPC) was made on a
series of 16 out of 18 patients with palpable nodules who underwent fine-ne
edle aspiration biopsy (FNAB) in our Department. The results of aspiration
biopsy were followed by histopathological examination of the surgically exc
ised tissues. There were three false-negative aspirations (16.6%), of which
two were probably bound to fine-needle sampling and one due to a mixture o
f benign and malignant cells which had originally gone unrecognized. The ac
curacy of the cytopathologic diagnosis in this variant was 88.8%.
An analysis of the diagnostic cytopathological criteria was performed, whic
h demonstrated the importance of both architectural features (monolayered a
nd branching sheets, microacinar structures, and their combinations) and nu
clear features (presence of nuclear grooves). Background-bound,features wer
e mainly represented by dense, nonfilamentous colloid.
The cytopathologic findings in FVPC were compared to those found in a serie
s of 10 usual papillary carcinomas (UPC) and 10 follicular neoplasms (FN).
These latter had originally been diagnosed by FNAB and were subsequently cl
assified histologically as follicular adenoma (n = 6), follicular carcinoma
(n = 3), or adenomatoid colloid nodule (n = 1).
Statistical evaluation was performed on the cytopathological findings in th
e three classes of lesions (FVPC. UPC, and FN) as to their presence and rel
ative frequency or absence by using a nonparametric one-way ANOVA (Kruskall
-Wallis) and, where necessary, a Mann-Whitney U test.
Papillary cellular fragments and multinucleated giant cells (P < 0.005), no
nfilamentous dense colloid, squamoid cells, and syncytia were significantly
more represented in UPC than in FVPC (P < 0.05), while histiocytes were si
gnificantly more frequent in FVPC (P < 0.005). Other nuclear and/or backgro
und features were significant only in the distinction between papillary car
cinomas as a group and FN.
The cytological differential diagnosis of the FVPC is briefly discussed wit
h relevance to the possible pitfalls caused by its peculiar cyto- and histo
morphology. <(c)> 2001 Wiley-Liss, Inc.