Adrenocortical carcinoma historical perspective: Difference between revisions
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==Overview== | ==Overview== | ||
In 1893, Grawitz et al was the first one who described adrenocortical carcinoma (ACC) and falsely assumed it | In 1893, Grawitz et al was the first one who described adrenocortical carcinoma (ACC), and falsely assumed that it was [[hypernephroma]]. By 1938, the Mayo group had removed [[Tumor|tumors]] successfully from 16 consecutive [[patients]], most of whom had [[Cushing's syndrome|Cushing’s syndrome.]] In 1960, [[mitotane]] was first used clinically to treat [[inoperable]] or recurrent ACC. | ||
==Historical perspective== | ==Historical perspective== | ||
* In 1811, an association of [[virilization]] and an [[adrenal tumor]] was first observed during an [[autopsy]]. | * In 1811, an association of [[virilization]] and an [[adrenal tumor]] was first observed during an [[autopsy]]. | ||
* In 1890, [[virilization]] was first documented following [[resection]] of an [[Adrenal tumor|adrenal tumor.]] | * In 1890, [[virilization]] was first documented following [[resection]] of an [[Adrenal tumor|adrenal tumor.]] | ||
* In 1893, Grawitz et al was the first one who described ACC and falsely assumed it | * In 1893, Grawitz et al was the first one who described ACC and falsely assumed it was a [[hypernephroma]].<ref name="pmid8661638">{{cite journal| author=Welbourn RB| title=Highlights from endocrine surgical history. | journal=World J Surg | year= 1996 | volume= 20 | issue= 5 | pages= 603-12 | pmid=8661638 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8661638 }}</ref> | ||
* In 1934, Walters et al | * In 1934, Walters et al described [[Cushing's syndrome]] in patients with [[Adrenal tumor|adrenal tumors]] and emphasized that the characteristic findings were not exclusively related to the [[Pituitary disease|pituitary disease.]]<ref name="pmid17856387">{{cite journal| author=Walters W, Wilder RM, Kepler EJ| title=THE SUPRARENAL CORTICAL SYNDROME WITH PRESENTATION OF TEN CASES. | journal=Ann Surg | year= 1934 | volume= 100 | issue= 4 | pages= 670-88 | pmid=17856387 | doi= | pmc=1390421 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=17856387 }}</ref> | ||
* In 1899, Knowsly Thornton of London was the first surgeon to successfully remove | * In 1899, Knowsly Thornton of London was the first surgeon to successfully remove the [[Adrenal cancer|adrenal cancer.]] | ||
* From 1905 to 1929, a number of patients were described with what was termed the [[adrenogenital syndrome]] and others with [[Adrenal tumor|adrenal tumors]] with [[virilism]]. | * From 1905 to 1929, a number of patients were described with what was termed the [[adrenogenital syndrome]] and others with [[Adrenal tumor|adrenal tumors]] with [[virilism]]. | ||
* By 1933, there was a clear evidence that the [[Pituitary gland|pituitary]] secretes an [[adrenocortical]] factor which was later recognized as [[Adrenocorticotropic hormone|ACTH.]]<ref name="pmid6878723">{{cite journal| author=Klammer A, Morger R| title=Successful treatment of an adrenocortical carcinoma. | journal=Prog Pediatr Surg | year= 1983 | volume= 16 | issue= | pages= 117-20 | pmid=6878723 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6878723 }}</ref> | * By 1933, there was a clear evidence that the [[Pituitary gland|pituitary]] secretes an [[adrenocortical]] factor which was later recognized as [[Adrenocorticotropic hormone|ACTH.]]<ref name="pmid6878723">{{cite journal| author=Klammer A, Morger R| title=Successful treatment of an adrenocortical carcinoma. | journal=Prog Pediatr Surg | year= 1983 | volume= 16 | issue= | pages= 117-20 | pmid=6878723 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6878723 }}</ref> | ||
Latest revision as of 16:49, 30 October 2017
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Adrenocortical carcinoma Microchapters |
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Differentiating Adrenocortical carcinoma from other Diseases |
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Diagnosis |
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Treatment |
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Case Study |
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Adrenocortical carcinoma historical perspective On the Web |
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American Roentgen Ray Society Images of Adrenocortical carcinoma historical perspective |
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Risk calculators and risk factors for Adrenocortical carcinoma historical perspective |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mohammed Abdelwahed M.D[2]
Overview
In 1893, Grawitz et al was the first one who described adrenocortical carcinoma (ACC), and falsely assumed that it was hypernephroma. By 1938, the Mayo group had removed tumors successfully from 16 consecutive patients, most of whom had Cushing’s syndrome. In 1960, mitotane was first used clinically to treat inoperable or recurrent ACC.
Historical perspective
- In 1811, an association of virilization and an adrenal tumor was first observed during an autopsy.
- In 1890, virilization was first documented following resection of an adrenal tumor.
- In 1893, Grawitz et al was the first one who described ACC and falsely assumed it was a hypernephroma.[1]
- In 1934, Walters et al described Cushing's syndrome in patients with adrenal tumors and emphasized that the characteristic findings were not exclusively related to the pituitary disease.[2]
- In 1899, Knowsly Thornton of London was the first surgeon to successfully remove the adrenal cancer.
- From 1905 to 1929, a number of patients were described with what was termed the adrenogenital syndrome and others with adrenal tumors with virilism.
- By 1933, there was a clear evidence that the pituitary secretes an adrenocortical factor which was later recognized as ACTH.[3]
- By 1938, the Mayo group had removed tumors successfully from 16 consecutive patients, most of whom had Cushing’s syndrome.
- In 1949, cortisol was discovered for the first time as a preparation.[4]
- Between 1930 and 1949, nearly 300 patients with ACC were published.
- In 1949, the first patient with Cushing’s disease was treated with pre-operative cortisol.
- By 1955, Tait and Simpson in London and Reichstein in Basel had isolated and prepared aldosterone for clinical use as fludrocortisone.
- By 1957, an intravenous preparation of cortisol, hydrocortisone, was used for the first time intraoperatively and in urgent situations of adrenal insufficiency.[5]
- In 1960, mitotane was first used clinically to treat inoperable or recurrent ACC.
References
- ↑ Welbourn RB (1996). "Highlights from endocrine surgical history". World J Surg. 20 (5): 603–12. PMID 8661638.
- ↑ Walters W, Wilder RM, Kepler EJ (1934). "THE SUPRARENAL CORTICAL SYNDROME WITH PRESENTATION OF TEN CASES". Ann Surg. 100 (4): 670–88. PMC 1390421. PMID 17856387.
- ↑ Klammer A, Morger R (1983). "Successful treatment of an adrenocortical carcinoma". Prog Pediatr Surg. 16: 117–20. PMID 6878723.
- ↑ RAPAPORT E, GOLDBERG MB, GORDAN GS, HINMAN F (1952). "Mortality in surgically treated adrenocortical tumors. II. Review of cases reported for the 20 year period 1930-1949, inclusive". Postgrad Med. 11 (4): 325–53. PMID 14920312.
- ↑ MACFARLANE DA (1958). "Cancer of the adrenal cortex; the natural history, prognosis and treatment in a study of fifty-five cases". Ann R Coll Surg Engl. 23 (3): 155–86. PMC 2413691. PMID 13571886.