S. Pilotti et al., POORLY DIFFERENTIATED FORMS OF PAPILLARY THYROID-CARCINOMA - DISTINCTIVE ENTITIES OR MORPHOLOGICAL PATTERNS, Seminars in diagnostic pathology, 12(3), 1995, pp. 249-255
The concept that poorly differentiated carcinomas (PDC) represent a gr
oup in an intermediate position in the spectrum of follicular cell-der
ived carcinomas of the thyroid gland is currently well established. Be
cause at the well-differentiated end of the spectrum there are two gro
ups of entities with distinct biological characteristics, ie, the papi
llary carcinoma (PC) and the follicular carcinoma (FC), we examined th
e group represented by PCs to ascertain whether papillary carcinoma-re
lated PDCs (pPDC) represent merely a histologic variant or a distinct
pathologic entity. For this purpose 227 consecutive PCs were reclassif
ied according to current criteria. The association between the presenc
e of a tumoral pattern consistent with pPDC (response variable), and p
rognostic factors such as gender age, pTNM (predictive variables) was
evaluated in terms of odds ratio statistics. One hundred eighty-three
of 227 cases, defined as PCs met the World Health Organization criteri
a of the not otherwise specified (NOS) (79 cases), microcarcinoma (65
cases), encapsulated (4 cases) and follicular (35 cases) variants. For
ty-four cases, defined as pPDCs, met those of the tall cell (39 cases)
, columnar cell PC (2 cases) and mixed tall cell-columnar cell PC (3 c
ases) variants, Statistical analyses of the two groups of patients sho
wed a significant correlation between differentiation and age above 40
years, extrathyroid tumor extension and low ratio of regional nodal i
nvolvement at the onset of disease. More strikingly they also showed t
hat morphology, ie, a tumoral pattern consistent with pPDC (differenti
ation), is the strongest predictor of biological behavior including re
currences and recurrence-related deaths that appear to occur five and
twenty times more frequently in pPDCs than in PCs, respectively. On th
e basis of these findings, we conclude that pPDCs represent a distinct
high-risk clinicopathologic entity among PCs. Copyright (C) 1995 by W
.B. Saunders Company