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Hypopituitarism as unusual sequelae to central nervous system tuberculosis

Neurological tuberculosis can very rarely involve the hypophysis cerebri. We report a case of an eighteen year old female who presented with five months duration of generalised apathy, secondary amenorrhea and weight gain. She was on irregular treatment for tuberculosis of the central nervous system...

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Autores principales: Mageshkumar, S., Patil, Devendra V., Philo, Aarthy J. A., Madhavan, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183520/
https://www.ncbi.nlm.nih.gov/pubmed/22029037
http://dx.doi.org/10.4103/2230-8210.84881
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author Mageshkumar, S.
Patil, Devendra V.
Philo, Aarthy J. A.
Madhavan, K.
author_facet Mageshkumar, S.
Patil, Devendra V.
Philo, Aarthy J. A.
Madhavan, K.
author_sort Mageshkumar, S.
collection PubMed
description Neurological tuberculosis can very rarely involve the hypophysis cerebri. We report a case of an eighteen year old female who presented with five months duration of generalised apathy, secondary amenorrhea and weight gain. She was on irregular treatment for tuberculosis of the central nervous system for the last five months. Neuroimaging revealed sellar and suprasellar tuberculomas and communicating hydrocephalus requiring emergency decompression. Endocrinological investigation showed hypopituitarism manifesting as pituitary hypothyroidism, hypocortisolism, hypogonadotropic hypogonadism, and hyperprolactinemia. Restarting anti-tuberculosis treatment, hormone replacement therapy, and a ventriculo-peritoneal shunt surgery led to remarkable improvement in the general condition of the patient.
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spelling pubmed-31835202011-10-25 Hypopituitarism as unusual sequelae to central nervous system tuberculosis Mageshkumar, S. Patil, Devendra V. Philo, Aarthy J. A. Madhavan, K. Indian J Endocrinol Metab Case Report Neurological tuberculosis can very rarely involve the hypophysis cerebri. We report a case of an eighteen year old female who presented with five months duration of generalised apathy, secondary amenorrhea and weight gain. She was on irregular treatment for tuberculosis of the central nervous system for the last five months. Neuroimaging revealed sellar and suprasellar tuberculomas and communicating hydrocephalus requiring emergency decompression. Endocrinological investigation showed hypopituitarism manifesting as pituitary hypothyroidism, hypocortisolism, hypogonadotropic hypogonadism, and hyperprolactinemia. Restarting anti-tuberculosis treatment, hormone replacement therapy, and a ventriculo-peritoneal shunt surgery led to remarkable improvement in the general condition of the patient. Medknow Publications 2011-09 /pmc/articles/PMC3183520/ /pubmed/22029037 http://dx.doi.org/10.4103/2230-8210.84881 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mageshkumar, S.
Patil, Devendra V.
Philo, Aarthy J. A.
Madhavan, K.
Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title_full Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title_fullStr Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title_full_unstemmed Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title_short Hypopituitarism as unusual sequelae to central nervous system tuberculosis
title_sort hypopituitarism as unusual sequelae to central nervous system tuberculosis
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3183520/
https://www.ncbi.nlm.nih.gov/pubmed/22029037
http://dx.doi.org/10.4103/2230-8210.84881
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