Atypical Presentation of Clinically Non-Functioning Pituitary Macroadenoma: Case Report of Concurrent Graves' Disease and Multi-Axis Pituitary Hypofunction in a 40-Year-Old Female

Authors

  • Rizkha Amaliya Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  • Dolly Irfandy Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  • Hesty Lidya Ningsih Department of Neurosurgery, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  • Alexander Kam Department of Internal Medicine, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  • Mardijas Efendi Department of Ophthalmology, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia

DOI:

https://doi.org/10.37275/bsm.v10i6.1610

Keywords:

Bitemporal hemianopsia, Endoscopic surgery, Graves disease, Hypopituitarism, Pituitary adenoma

Abstract

Background: Non-functioning pituitary adenomas (NFPAs) present variable clinical manifestations depending on tumor size and location. Concurrent primary autoimmune thyroid disease in NFPA patients is exceptionally rare and requires careful diagnostic distinction from secondary hypothyroidism.  

Case presentation: A 40-year-old female presented with progressive bilateral peripheral vision narrowing over 3 months, chronic bifrontal headaches, secondary amenorrhea, and nocturia-predominant polyuria. Neuro-ophthalmologic examination revealed bitemporal hemianopsia with visual acuity 20/200 left eye and 20/25 right eye. Endocrine evaluation demonstrated: primary hyperthyroidism (TSH 0.02 µIU/mL, FT4 28.32 pmol/L, positive thyroid receptor antibodies), secondary adrenal insufficiency (cortisol 1 µg/dL, ACTH <5 pg/mL), and hypogonadotropic hypogonadism (LH 1.62 IU/L). Neuroimaging revealed a 2.13 × 2.28 × 3.05 cm sellar/suprasellar lesion with optic chiasm compression (Knosp Grade II). Endoscopic transsphenoidal surgery achieved complete gross total resection. Histopathology confirmed null-cell adenoma with low Ki-67 proliferation index (2%).

Conclusion: Postoperative course was uncomplicated with rapid visual field improvement, complete resolution of bitemporal hemianopsia by 2 weeks, and normalization of all endocrine axes by 12 weeks, including menstrual recovery and gonadal axis restoration. This case illustrates the diagnostic challenge of distinguishing secondary hyperprolactinemia from primary prolactinoma in NFPA, the rarity of concurrent Graves' disease with pituitary macroadenoma, and favorable outcomes with complete surgical decompression achieving multisystem endocrine recovery.

Authors

  • Rizkha Amaliya1
  • Dolly Irfandy1*
  • Hesty Lidya Ningsih2
  • Alexander Kam3
  • Mardijas Efendi4
  1. 1Department of Otorhinolaryngology-Head and Neck Surgery, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  2. 2Department of Neurosurgery, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  3. 3Department of Internal Medicine, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia
  4. 4Department of Ophthalmology, Faculty of Medicine, Universitas Andalas/Dr. M. Djamil General Hospital, Padang, Indonesia

Corresponding author Dolly Irfandy — dollyirfandy@med.unand.ac.id

Article history

  1. Submitted
  2. Accepted
  3. Published

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Published

2026-04-16

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How to Cite

1.
Rizkha Amaliya, Dolly Irfandy, Hesty Lidya Ningsih, Alexander Kam, Mardijas Efendi. Atypical Presentation of Clinically Non-Functioning Pituitary Macroadenoma: Case Report of Concurrent Graves’ Disease and Multi-Axis Pituitary Hypofunction in a 40-Year-Old Female. Bioscmed [Internet]. 2026 Apr. 16 [cited 2026 Aug. 12];10(6):2212-23. Available from: https://bioscmed.com/index.php/bsm/article/view/1610

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