Adrenocortical neoplasms are rare in childhood. Their histopathological categorization into
benign and malignant is often challenging, impacting further management. While the …

Objective Primary adrenal malignant tumor is rare. The factors affecting the prognosis
remain poorly defined. This study targeted to construct and corroborate a model for …

Adrenocortical carcinoma (ACC) is a rare but very aggressive endocrine malignancy with
poor survival. Histopathology is important for diagnosis, while in some cases …

Background The prognostic significance of tumor size with adrenocortical carcinoma (ACC)
patients has not yet been thoroughly evaluated. Our objective was to investigate the …

Background Current diagnostic criteria of adrenocortical neoplasms are mostly based on
morphology. The utility of immunohistochemistry (IHC) and histochemistry is limited …

Background Primary malignant adrenal tumors were rare and had a poor prognosis. This
investigation aimed to create a useful clinical prediction nomogram to anticipate cancer …

Objective: Rare disease Background: Adrenocortical carcinoma (ACC) is a rare malignancy
associated with unfavorable prognosis. It is mainly diagnosed in the fifth or sixth decade of …

Adrenocortical carcinoma (ACC) is a rare endocrine malignancy arising from the adrenal
cortex often with unexpected biological behavior. It can occur at any age, with two peaks of …

Major technological advances in genomics have made it possible to identify critical genetic
alterations in cancer, rendering oncology well along the path to personalised cancer …

Background: Primary malignant adrenal tumors were rare and had a poor prognosis. This
investigation aimed to create a useful clinical prediction nomogram to anticipate cancer …