Article contents

Articles

A Case of Hoffman Syndrome Masquerading as Pituitary Tumour

Authors

  • Dr Manish Bhartiya , Dr Arnab Ghosh , Dr Yashpal Singh , Dr V Sashindhran MBBS, Resident MD (Medicine), Armed Forces Medical College, Sholapur Road, Wanowrie, Pune, Maharashtra, India, PIN-411 040,

Abstract

Hoffman syndrome, a rare presentation of hypothyroidism, is characterized by pseudo-hypertrophy and stiffness of muscles, myxoedematous features. Long standing hypothyroidism can cause pituitary hyperplasia which is difficult to distinguish with pituitary adenoma even with contrast MRI. We describe a case of a 48 years old male presenting as ‘Hoffman syndrome’ with reactive pituitary hyperplasia that mimicked a pituitary macroadenoma. After 20 days of thyroid hormone therapy, the patient had improvement of the muscular cramps. After 03 months of active therapy a repeat MRI was done which showed regression of size of the mass. In a case of primary hypothyroidism with a solid mass lesion of the pituitary gland, pituitary hyperplasia secondary to hypothyroidism rather than pituitary adenoma should be excluded to avoid unnecessary surgical intervention which has its own complications.

Article information

Journal

International Journal of Medical Science and Clinical Invention

Volume (Issue)

4 (1)

Pages

Published

2017-01-20

How to Cite

A Case of Hoffman Syndrome Masquerading as Pituitary Tumour. (2017). International Journal of Medical Science and Clinical Invention, 4(1). https://doi.org/10.18535/ijmsci/v4i1.18

Downloads

Views

195

Downloads

161