RARE CASE OF PINEAL GERMINOMA WITH ARGININE VASOPRESSIN DEFICIENCY

Authors

  • Mohamad Firdaus Barakath
  • Vijayrama Rao Sambamoorthy
  • Anilah Abdul Rahim
  • Ijaz Hallaj Rahmatullah

Keywords:

GERMINOMA, ARGININE, VASOPRESSIN

Abstract

INTRODUCTION/BACKCGROUND
Pineal tumour is an uncommon type of brain tumour in Malaysia, with low incidence rate of 2.1% based on a demographic study done in 1 of the states in Peninsular Malaysia. On the other hand, germinoma is a common cause of intracranial tumor leading to arginine vasopressin deficiency (AVP-D). In a literature review, 82% of 95 patients were diagnosed with AVP-D.

CASE
We report a case of a 22-year-old Malay male, who was diagnosed with pineal gland tumour complicated with obstructive hydrocephalus. He underwent endoscopic biopsy of pineal region tumor and right ventriculoperitoneal shunt insertion in January 2024. Two days after his surgical intervention, he developed an episode of polyuria with urine output more 5 ml/kg/hr for consecutive hours in the ward without any accompanying thirst. Investigations showed high serum osmolarity of 294 mOsm/kg (NR: 271-286 mOsm/kg) with inappropriately low urine osmolarity of 161 mOsm/kg (NR: 300-900 mOsm/ kg). He was diagnosed with AVP-D and responded well to intravenous desmopression (DDAVP), a vasopressin synthetic analogue, with reduction in urine volume and passing more concentrated urine. Over the next few days, he started to develop more episodes of polyuria, requiring regular dosing of desmopressin. The tissue histopathology of the pineal gland revealed germ cell tumour consistent with germinoma.

CONCLUSION
AVP-D is a known complication of intracranial germ cell tumour. Our case report shows that AVP-D may also happen as a consequence of neurosurgical intervention. Careful clinical and biochemical postoperative monitoring remains essential to correctly diagnose and manage AVP-D following neurosurgery intervention.

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Author Biographies

Mohamad Firdaus Barakath

Endocrine Unit, Hospital Raja Permaisuri Bainun, Ipoh, Malaysia

Vijayrama Rao Sambamoorthy

Endocrine Unit, Hospital Raja Permaisuri Bainun, Ipoh, Malaysia

Anilah Abdul Rahim

Endocrine Unit, Hospital Raja Permaisuri Bainun, Ipoh, Malaysia

Ijaz Hallaj Rahmatullah

Endocrine Unit, Hospital Raja Permaisuri Bainun, Ipoh, Malaysia

References

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Published

2024-07-17

How to Cite

Barakath, M. F., Sambamoorthy, V. R., Rahim, A. A., & Rahmatullah, I. H. (2024). RARE CASE OF PINEAL GERMINOMA WITH ARGININE VASOPRESSIN DEFICIENCY. Journal of the ASEAN Federation of Endocrine Societies, 39(S1), 82. Retrieved from https://asean-endocrinejournal.org/index.php/JAFES/article/view/4675

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