Panhypopituitarism due to Sheehan’s Syndrome in a Patient with Recurrent Hyponatremia: Case Report from Nepal

Authors

  • Sudip Niroula National Medical College Teaching Hospital, Birgunj, Parsa, Nepal
  • Anil Kumar Shah National Medical College Teaching Hospital, Birgunj, Parsa, Nepal

DOI:

https://doi.org/10.3126/medphoenix.v8i2.61827

Keywords:

Chronic Severe Hyponatremia, Panhypopituitarism, Sheehan’s Syndrome

Abstract

Introduction: Panhypopituitarism, deficiency of all pituitary hormones (anterior pituitary hormones: adrenocorticotropic hormone, thyroid-stimulating hormone, luteinizing hormone, follicle-stimulating hormone, prolactin, growth hormone; posterior pituitary hormones: oxytocin, vasopressin). Sheehan’s syndrome also known as postpartum hypopituitarism is one of the causes of panhypopituitarism, which is characterized by hypopituitarism due to necrosis of pituitary gland secondary to massive postpartum hemorrhage. In this case, a 50 years female presented with the history of vomiting and loss of appetite since 2 years with severe hyponatremia, and decreased pituitary hormones levels in laboratory findings with significant obstetric history is diagnosed with Sheehan’s Syndrome.

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Published

2023-12-31

How to Cite

Niroula, S., & Shah, A. K. (2023). Panhypopituitarism due to Sheehan’s Syndrome in a Patient with Recurrent Hyponatremia: Case Report from Nepal. Med Phoenix, 8(2), 66–69. https://doi.org/10.3126/medphoenix.v8i2.61827

Issue

Section

Case Reports