1991PubMedRequires access

[Adrenocortical carcinoma and its treatment with mitotane. Description of a case].

Anna Julia Ferrari Parma, B D'agnolo

Open publisher page 0 citations

Abstract

Adrenocortical carcinoma is a rare tumor with a poor prognosis. The clinical features and rational bases of pharmacologic therapy of adrenocortical carcinoma are discussed in the light of the case of a patient with a bulky, inoperable tumor whose treatment with mitotane was followed by a dramatic regression though several, important side effects.

About this research paper

What this paper is about

Adrenocortical carcinoma is a rare tumor with a poor prognosis. The clinical features and rational bases of pharmacologic therapy of adrenocortical carcinoma are discussed in the light of the case of a patient with a bulky, inoperable tumor whose treatment with mitotane was followed by a dramatic regression though several, important side effects.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Adrenocortical carcinoma is a rare tumor with a poor prognosis. The clinical features and rational bases of pharmacologic therapy of adrenocortical carcinoma are discussed in the light of the case of a patient with a bulky, inoperable tumor whose treatment with mitotane was followed by a dramatic regression though several, important side effects.

Key concepts: Mitotane, Adrenocortical carcinoma, Medicine, Carcinoma, Oncology, Internal medicine

Related papers

Back to paper searchBrowse research topicsOriginal source
[Adrenocortical carcinoma and its treatment with mitotane. Description of a case]. — Research Paper | ScholarLens