Neurofibromatosis type 1 and lymphocytic hypophysitis: Single trigger and double shots?

Authors

  • Jyothi Idiculla St John's Medical College Bangalore-560034 Karnataka
  • Shine Pakalomattom
  • Anasuya Desai
  • Babu Philip
  • Vineeta Shobha

DOI:

https://doi.org/10.15305/ijrci/v3i1/104

Keywords:

lymphocytic hypophysitis, neurofibromatosis 1

Abstract

Lymphocytic hypophysitis, an inflammatory disorder of the pituitary stalk and gland, can cause multiple hormone deficiencies. The disease is considered to be of autoimmune etiology. We report here a case of lymphocytic hypophysitis with cortisol deficiency in an 18-year-old female who had been previously diagnosed with neurofibromatosis type 1. The case study also discusses the role of neurofibromin gene in autoimmunity and possible pathogenesis.

Author Biography

Jyothi Idiculla, St John's Medical College Bangalore-560034 Karnataka

Additional Professor

References

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Ingram DA, Zhang L, McCarthy J, Wenning MJ, Fisher L, Yang F-C, et al. Lymphoproliferative defects in mice lacking the expression of neurofibromin: functional and biochemical consequences of Nf1 deficiency in T-cell development and function. Blood. 2002 Nov 15;100(10):3656–62.

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Published

20-03-2015

Issue

Section

Case Studies