No abstract available.
Adrenocortical Carcinoma*

No abstract available.
Adrenocortical Carcinoma

No abstract available.
Adrenocortical Carcinoma*

Adrenocortical carcinoma (ACC) is a rare and aggressive neoplasm with poor prognosis. We report a case of a 30-year-old female who presented with profound classic features of an adrenocorticotrophic hormone (ACTH)-independent Cushing’s syndrome (CS) and a large adrenal mass with massive venous tumor thrombosis of the entire inferior vena cava (IVC), left renal and adrenal veins confirmed by imaging. Adrenal biopsy histopathology and immunohistochemistry confirmed ACC. Systemic palliative chemotherapy was administered. This rare case presents a unique and atypical presentation of an extensive tumor thrombosis of IVC. With the advanced stage at diagnosis, aggressive nature and poor prognosis of the disease, there is still a need to determine viable therapeutic options for metastatic ACC associated with venous invasion.
Adrenocortical Carcinoma

No abstract available.
Adrenocortical Carcinoma* ; Female* ; Humans

Adrenal cortical carcinoma is classified clinically as functioning and nonfunctioning and the latter is though to be extremely rare and causes generally mass effect or symptoms due to metastasis because of insufficient steroid secretion. We report a case of nonfunctioning adrenal cortical carcinoma, which is thought to be heterotopic origin.
Adrenocortical Carcinoma* ; Neoplasm Metastasis

No abstract available.
Adrenocortical Carcinoma* ; Stomach Neoplasms*

Nonfunctioning adrenal cortical carcinoma is extremely rare, which probably merely secreted insufficient steroid to cause signs and symptoms. We experienced a case of nonfunctioning adrenal cortical carcinoma without metastatic evidence, treated by only adrenalectomy.
Adrenalectomy ; Adrenocortical Carcinoma*

The identification of fat density by unenhanced CT within an adrenal mass is highly suggestive of myelolipoma. Adrenal collision tumors which involve a myelolipoma are uncommon, though the involvement of adenomas and pheochromocytomas has been reported. We describe a case in which an adrenal collision tumor consisting of an adrenocortical carcinoma and myelolipoma, presented as a large fat-containing adrenal soft tissue mass.
Adenoma ; Adrenocortical Carcinoma* ; Myelolipoma* ; Pheochromocytoma

Adrenocortical carcinoma is a rare tumor in children. This tumor is more likely to be hormonally active in children than in adults and tends to cause a variety of symptoms. These tumors are usually diagnosed at the advanced stages and have a dismal prognosis. Here we report a case of a functioning adrenocortical carcinoma in a child with a review of the relevant literature.
Adrenocortical Carcinoma* ; Adult ; Child* ; Humans ; Prognosis ; Virilism