Histopathological Criteria for Paediatric Adrenocortical Carcinoma

Abstract

<b><i>Introduction:</i></b> Adrenocortical carcinoma (ACC) is diagnosed in paediatric patients at 5 months after symptom onset on average, and 38% die during the first 2.5 years of follow-up. This study aimed to compare the accuracy of Weiss, Van Slooten, and Wieneke histopathological ACC classifications for predicting follow-up prognosis in a paediatric population. <b><i>Methods:</i></b> Data were retrieved from medical records of 57 patients aged &#x3c;18 years who underwent surgical treatment for ACC with surgical follow-up over 6 months or death due to ACC. They were classified into either good (without recurrence/death due to ACC) or poor (with recurrence/death due to ACC) prognosis group. Two expert pathologists classified the ACC surgical specimens according to the Weiss, Van Slooten, and Wieneke criteria. <b><i>Results:</i></b> The median follow-up duration was 126 (18–225) months in 38 males (66.7%) and 19 females (33.3%) (median age: 3 [1–6.5] years). The good prognosis group was younger than the poor prognosis group (median age: 3 [1.5–6.2] years vs. 5 [2–10] years). Seventeen (29.8%) patients in the poor prognosis group died due to ACC within the first 50 months of surgical follow-up; the earliest death occurred in the fourth follow-up month, and the majority of deaths occurred within 24 months of follow-up. The accuracies of Weiss, Van Slooten, and Wieneke classification systems were 40%, 47%, and 77%, respectively. <b><i>Discussion/Conclusion:</i></b> The Wieneke classification showed the best accuracy but was not sufficiently precise to establish reliable prognosis for ACC in the paediatric population. The Wieneke classification had approximately 95% sensitivity and negative predictive value.