Title: Episodic Hypertension, Left Heart Failure, Head Ache, Due to Pheochromocytoma (Adrenal Gland)

Authors: Dr Kumar Avijeet Dash, Dr Vishnu K, Dr B.K.Behera, Dr C R Khatua, Dr S Pati, Dr Sooraj Menon R, Dr Roniya Simethy

 DOI:  http://dx.doi.org/10.18535/jmscr/v4i8.101

Abstract

The diagnosis of pheachromocytoma requires a high degree of clinical suspicion, because of its rare incidence and also the signs and symptoms of this disease is episodic and presents with complications, like heart failure like in our case. As few of cases are malignant, most of patients can be cured for which early diagnosis is essential.

KEY WORDS: Pheachromocytoma, NET (neuro endocrine tumor), MEN (multiple endocrine neoplasia), left ventricular failure (LVF), left ventricular hypertrophy (LVH)

References

 

1.             William F.young, JR. Endocrine hypertension: Williams textbook of Endocrinology.12th edition.2013; (16): 547-562.

2.              Hartmut P.H. Neumann. Pheochromo-cytoma: Harrison`s Principles Of Internal Medicine.19th Edition. 2015 ;(407):2329-2334.

3.     Guido Laitra,Adam whaley-connell and James R Sower. Pheochromocytoma: Manual of endocrinology and metabolism .4th edition.2012;(13):160-167

Corresponding Author

Dr C R Khatua

Assistant Professor, Department of Medicine

MKCG Medical College, Berhampur, Odisha