AIM: To confirm the potential association between autoimmune thyroid diseases (AITD) and papillary thyroid carcinoma (PTC) in a prospective study in unselected thyroid nodules (TN). PATIENTS AND METHODS: One-hundred-eighty-four patients (235 TN) consecutively submitted to fine-needle aspiration cytology (FNAC), fully evaluated for associated AITD. In most FNAC samples, BRAFV600E mutation was evaluated by PCR and RET-PTC rearrangements by PCR and interphase fluorescence in situ hybridization (I-FISH), using a newly developed homebrew dual-color-breakpart RET probe. In 61 operated patients (75 TN), histology and lymphocytic thyroid infiltration (LTI) description were available. RESULTS: Higher prevalence of suspicious/malignant cytology was found in AITD+ TN (22.6% vs 9.8% in AITD-, p<0.01). Prevalence of PTC in operated TN was higher in AITD+ (68.8%) than in AITD- (44.2%, p<0.05) and LTI was found in 66% of malignant vs 34% of benign TN (p <0.05). BRAFV600E mutation was found in 11/93 (11.8%) AITD+ vs 2/142 (1.4%) AITD- TN (p<0.001), all PTC. BRAFV600E mutation was found in 11/22 (50%) AITD+ and in 2/17 (11.8%; p<0.02) AITD- PTC. RET-PTC rearrangements were found by PCR only in 3 FNAC (one AITD+ and two AITD-) all showing a separate breakapart I-FISH signal in ≥ 6.8% nuclei. When compared to normal thyroid, broken signal (cutoff ≥3%, mean±3DS), was found in a larger number of FNAC distributed along the whole cytological spectrum, with higher prevalence in indeterminate to suspicious/malignant (13.6%) vs benign (3.1%) cytology, but no correlation was observed between broken I-FISH signal and AITD. CONCLUSIONS: A significant association between AITD and PTC was confirmed in a prospective study of TN submitted to FNAC. This association does not appear to be mediated by RET-PTC rearrangements. The higher prevalence of BRAFV600E mutation in PTC associated with AITD will deserve further investigation.
Thyroid autoimmunity and thyroid cancer: pathological and molecular study in a longitudinal series of unselected nodules.
Boi F;Caria P;Borghero A;Frau DV;Cappai A;Dettori T;Riola A;Maurelli I;Lai ML;Calò PG;Nicolosi A;Vanni R;Mariotti S.
2011-01-01
Abstract
AIM: To confirm the potential association between autoimmune thyroid diseases (AITD) and papillary thyroid carcinoma (PTC) in a prospective study in unselected thyroid nodules (TN). PATIENTS AND METHODS: One-hundred-eighty-four patients (235 TN) consecutively submitted to fine-needle aspiration cytology (FNAC), fully evaluated for associated AITD. In most FNAC samples, BRAFV600E mutation was evaluated by PCR and RET-PTC rearrangements by PCR and interphase fluorescence in situ hybridization (I-FISH), using a newly developed homebrew dual-color-breakpart RET probe. In 61 operated patients (75 TN), histology and lymphocytic thyroid infiltration (LTI) description were available. RESULTS: Higher prevalence of suspicious/malignant cytology was found in AITD+ TN (22.6% vs 9.8% in AITD-, p<0.01). Prevalence of PTC in operated TN was higher in AITD+ (68.8%) than in AITD- (44.2%, p<0.05) and LTI was found in 66% of malignant vs 34% of benign TN (p <0.05). BRAFV600E mutation was found in 11/93 (11.8%) AITD+ vs 2/142 (1.4%) AITD- TN (p<0.001), all PTC. BRAFV600E mutation was found in 11/22 (50%) AITD+ and in 2/17 (11.8%; p<0.02) AITD- PTC. RET-PTC rearrangements were found by PCR only in 3 FNAC (one AITD+ and two AITD-) all showing a separate breakapart I-FISH signal in ≥ 6.8% nuclei. When compared to normal thyroid, broken signal (cutoff ≥3%, mean±3DS), was found in a larger number of FNAC distributed along the whole cytological spectrum, with higher prevalence in indeterminate to suspicious/malignant (13.6%) vs benign (3.1%) cytology, but no correlation was observed between broken I-FISH signal and AITD. CONCLUSIONS: A significant association between AITD and PTC was confirmed in a prospective study of TN submitted to FNAC. This association does not appear to be mediated by RET-PTC rearrangements. The higher prevalence of BRAFV600E mutation in PTC associated with AITD will deserve further investigation.I metadati presenti in IRIS UNICA sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono protetti da diritto d'autore, salvo diversa indicazione.


