A CASE REPORT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA ASSOCIATED WITH CUSHING SYNDROME

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

BORZOUEI SH.; SHEIKH V.; MOSAVI BAHAR S.H.; YOUSEFIAN A.; MAHERONNAGHSH R.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: Avicenna Journal of Clinical Medicine Year:2013 | Volume:20 | Issue:3 (SN 69) Page(s): 260-265

Download Full-Text

Persian Verion

View:

600

Download:

Cites:

Information Journal Paper

Title

A CASE REPORT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA ASSOCIATED WITH CUSHING SYNDROME

Author(s)

Keywords

MEDULLARY THYROID CARCINOMAQ2

MULTIPLE ENDOCRINE NEOPLASIA TYPE 2A PHEOCHROMOCYTOMAQ2

Abstract

Introduction: Multiple endocrine neoplasia type IIa (MEN IIa) is an autosomal dominant syndrome characterized bypheochromocytoma, MEDULLARY THYROID CARCINOMA and hyperparathyroidism.Pheochromocytoma approximately occurs in 50% of patients with MEN IIa. This tumor has the capacity to produce ACTH ectopically and becomes manifest like Cushing syndrome, although it is very rare.Case Report: We report a 26-year-old woman patient with severe muscle weakness, skin lesions in extremity, hypertension, new onset diabetes and in the laboratory data hypokalemia, metabolic alkalosis, high serum level of cortisol, metanephrine, normetanephrine, calcitonin and bilateral adrenal mass in computed tomography as the first clinical manifestations of an ACTH-secreting pheochromocytoma.Conclusion: In the patients with hypertension, new onset diabetes and hypokalemia Cushing syndrome and pheochromocytoma should always be ruled out.

Cites

No record.

References

No record.

Cite

APA: Copy

BORZOUEI, SH., SHEIKH, V., MOSAVI BAHAR, S.H., YOUSEFIAN, A., & MAHERONNAGHSH, R.. (2013). A CASE REPORT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA ASSOCIATED WITH CUSHING SYNDROME. AVICENNA JOURNAL OF CLINICAL MEDICINE (SCIENTIFIC JOURNAL OF HAMADAN UNIVERSITY OF MEDICAL SCIENCES AND HEALTH SERVICES), 20(3 (SN 69)), 260-265. SID. https://sid.ir/paper/17994/en

Vancouver: Copy

BORZOUEI SH., SHEIKH V., MOSAVI BAHAR S.H., YOUSEFIAN A., MAHERONNAGHSH R.. A CASE REPORT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA ASSOCIATED WITH CUSHING SYNDROME. AVICENNA JOURNAL OF CLINICAL MEDICINE (SCIENTIFIC JOURNAL OF HAMADAN UNIVERSITY OF MEDICAL SCIENCES AND HEALTH SERVICES)[Internet]. 2013;20(3 (SN 69)):260-265. Available from: https://sid.ir/paper/17994/en

IEEE: Copy

SH. BORZOUEI, V. SHEIKH, S.H. MOSAVI BAHAR, A. YOUSEFIAN, and R. MAHERONNAGHSH, “A CASE REPORT OF MULTIPLE ENDOCRINE NEOPLASIA TYPE IIA ASSOCIATED WITH CUSHING SYNDROME,” AVICENNA JOURNAL OF CLINICAL MEDICINE (SCIENTIFIC JOURNAL OF HAMADAN UNIVERSITY OF MEDICAL SCIENCES AND HEALTH SERVICES), vol. 20, no. 3 (SN 69), pp. 260–265, 2013, [Online]. Available: https://sid.ir/paper/17994/en

Related Journal Papers