HYPOPITUITARISM: A CASE REPORT OF OVERLOOKED DIAGNOSIS.

Author:

Shah Kiran1,Gandhi Charmi2,More Sneha2,Akluwar Shalini3,Tiwari Vishal4,Gupta Hemant5

Affiliation:

1. Visiting Diabetologist, Dept of Medicine, Grant Govt Medical College and Sir J.J Group of Hospitals, Mumbai

2. Junior Resident, Dept of Medicine, Grant Govt Medical College and Sir J.J Group of Hospitals, Mumbai.

3. Assistant Professor, Dept of Medicine ,Grant Govt Medical College and Sir J.J Group of Hospitals, Mumbai.

4. Senior Resident, Dept of Medicine, Grant Govt Medical College and Sir J.J Group of Hospitals, Mumbai.

5. Professor, Dept of Medicine Grant Govt Medical College and Sir J.J Group of Hospitals, Mumbai.

Abstract

Hypopituitarism, which has a number of causes, is a severe endocrine condition that needs early diagnosis and treatment to prevent serious consequences. We report a 17-year old male seen in outpatient department for lack of development of secondary sexual characters and short stature. Laboratory investigation showed low total tri-iodothyronine (T3) , low total thyroxine (T4) and slightly elevated thyroid stimulating hormone (TSH) , low basal cortisol, and normal prolactin level. The patient also had low total testosterone, low LH, and FSH values. Magnetic resonance imaging (MRI) of the pituitary revealed a hypoplastic anterior pituitary with ectopic posterior pituitary. This case highlights the notable absence of recognizing the clinical presentation of hypopituitarism which at times is nonspecic and often progress insidiously before a diagnosis is made. The case calls attention to importance of thorough history taking, attention, and observation in making a new diagnosis that has the potential to alter a patient's health care and quality of life.

Publisher

World Wide Journals

Reference14 articles.

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