Papillary thyroid carcinoma in paediatric age
Data
2020Autore
Garzi, Alfredo
Prestipino, Marco
Calabrò, Eleonora
Di Crescenzo, Rosa Maria
Rubino, Maria Serena
Metadata
Mostra tutti i dati dell'itemAbstract
In children, differentiated thyroid
carcinoma is a rare condition. Early diagnosis is not
always easy, because of the lack of clinical symptoms,
but it has a pivotal role in performing a correct
therapeutic process.
The study describes three cases of papillary
thyroid carcinoma. None of the three patients had a
positive familiarity or exposure to risk factors. In two
cases, the tumor occurred as a non-injurious swelling in
the anterior cervical region, in the other case it
occurred with a latero-cervical lymphadenopathy that
had been persistent for a year. In the first two patients
we made a certain diagnosis by the needle aspiration of
the thyroid nodule; in the other case the diagnosis was
made by surgical exeresis and histological analysis of
the lymph nodes. We also performed blood chemistry
and hormonal tests, neck ultrasound, chest x-ray.
The three children underwent total
thyroidectomy and two of them also underwent rightsided cervical lymph node exeresis because there was
the presence of metastasis.
In our experience, the best therapeutic strategy
for children with differentiated thyroid carcinoma is the
total thyroidectomy, followed or not by latero-cervical
lymph node exeresis and radioiodiotherapy. The
removal of the whole gland reduces the risk of relapse.