Home > Journals > Indian Journal of Pathology: Research and Practice

Indian Journal of Pathology: Research and Practice

Submit your article Read this Journals View all journals
Full Text (PDF)
Case Report

Phaechromocytoma of Adrenal Gland

Vaibhav Mane* , Vaibhav Mane* , V. R. Pawar** , Sushant Mohite***

Author Information

Licence:



Indian Journal of Pathology: Research and Practice 4(2):p 97-99, July - September 2015. | DOI: DOI : https://dx.doi.org/10.21088/ijprp.2278.148X.4215.10

How Cite This Article:

Timeline

Received : N/A         Accepted : N/A          Published : N/A

Abstract

 Pheochromocytoma is a rare catecholamine secreting tumour originating usually from adrenal medulla and produces signs and symptoms due excessive catecholamine secretion from tumour.Pheochromocytoma is a rare cause of hypertension. If the diagnosis of pheochromocytoma is overlooked, the consequences could be disastrous, even fatal; however, if a pheochromocytoma is identified, it is potentially curable, as being one of the cause of surgically correctable hypertension [1,2,3,5,6,9,10,11].

References

No records found.


About this article

Cite this article

Licence:



Received Accepted Published
N/A N/A N/A
DOI: DOI : https://dx.doi.org/10.21088/ijprp.2278.148X.4215.10

Keywords


Article Level Metrics

Last Updated

Monday 13 July 2026, 13:15:25 (IST)

2047

Accesses

2
434
00

Citations


NA
NA
NA

Download citation


Article Keywords

Keyword Highlighting

Highlight selected keywords in the article text.


Timeline

Received N/A
Accepted N/A
Published N/A

licence




Access this article

Reprint Order Form
Buy this Article
Institutional Subscriptions

Share