Background: Infantile adrenal cortical carcinoma is rare and, in diagnosis, requires careful examination.
Case: A 4-year-old girl showed an abdominal tumor and virilization, with elevated adrenal androgen in serum and urine. The resected adrenal tumor was encapsulated, soft and fragile, reddish-brown, 12.0×8.0-7.5cm, and 430g in weight, with a hemorrhagic necrotic cut section with cystic degeneration.
Cytology disclosed hypercellularity in the necrotic hemorrhagic background. Tumor cells showed loss of cohesion and were swollen with granular cytoplasm. They also had large hyperchromatic nuclei with coarse chromatin. Multinucleated cells and intranuclear inclusion were seen occasionally.
Histologically, tumor cells showed acidophilic cytoplasm forming diffuse solid nests. Nuclei of tumor cells were bizarre and hyperchromatic with occasional multinucleation.
Electron microscopy showed abundant smooth rough-surfaced ERs, round mitochondria with tubular cristae, lipid droplets, and irregularly shaped nuclei.
Conclusion: Histopathological and cytological findings of the tumor are analogous to those seen in androgen-producing adrenal cortical carcinoma (APACC).
When diagnosing a rare infantile APACC, sufficient examination with special reference to the extent of cellular atypism and tumor size is essential, requiring endocrinological findings.
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