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Pituitary macroadenoma with optic chiasm compression and hypopituitarism: a case report

Universa Medicina · Vol. 45 No. 1 (2026) · hlm. 81–87

DOI
10.18051/UnivMed.2026.v45.81-87
ISSN
2407-2230, 1907-3062
Terbit
2026-04-27
Penerbit
Faculty of Medicine, Universitas Trisakti
Bahasa
eng
Lisensi
creativecommons.org/licenses/by-nc-sa/4.0

Abstrak

INTRODUCTIONPituitary macroadenomas are benign pituitary tumors measuring more than 1 cm in diameter that constitute a substantial proportion of intracranial neoplasms. Despite their benign histology, these tumors may lead to significant morbidity due to local mass effects and endocrine dysfunction. Compression of the optic chiasm can result in progressive visual impairment and irreversible blindness if not promptly treated. Additionally, pituitary hormonal deficiencies may cause life-threatening metabolic and systemic complications. Early recognition and multidisciplinary management are therefore essential to prevent permanent sequelae and optimize functional recovery. Case DescriptionA 40-year-old woman presented with a one-year history of recurrent headaches accompanied by progressive blurring of vision, diplopia, and visual field defects. She also reported irregular menstruation and unintended weight loss. Brain magnetic resonance imaging demonstrated a 2.13 × 2.28 × 3.05 cm pituitary macroadenoma with a characteristic “snowman appearance” compressing the optic chiasm. Hormonal evaluation revealed secondary adrenal insufficiency, hypogonadotropic hypogonadism, suppressed thyroid-stimulating hormone (TSH) with elevated free thyroxine (T4), and hyperprolactinemia attributed to the stalk effect, consistent with hypopituitarism and thyroid dysfunction. Initial stabilization with hydrocortisone and methimazole was performed prior to definitive management. The patient subsequently underwent transsphenoidal tumor resection with appropriate perioperative glucocorticoid coverage. Postoperatively, she remained clinically stable with improvement in headache and visual symptoms, and continued hormonal therapy under close endocrinological supervision. ConclusionsThis case underscores the importance of comprehensive hormonal assessment, timely neurosurgical intervention, and coordinated multidisciplinary care in managing pituitary macroadenomas complicated by optic chiasm compression and hypopituitarism to achieve favorable clinical outcomes.

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  • Universitas Muhammadiyah Riau
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Rekan penulisOrganisasiArtikel bersama
Abdul Kadir JaelaniAfiliasi tidak diketahui2
Fadrian FadrianAfiliasi tidak diketahui2
Armen AhmadAfiliasi tidak diketahui2
Vidola Yasena PutriAfiliasi tidak diketahui2
Disa Hijratul MuharramahAfiliasi tidak diketahui2
Genta PradanaAfiliasi tidak diketahui2
Yanne Pradwi EfendiAfiliasi tidak diketahui2
Mulyanto MulyantoUniversitas Muhammadiyah Riau1
Itok Dwi KurniawanAfiliasi tidak diketahui1
Isharyanto IsharyantoAfiliasi tidak diketahui1
Sarjiyanto SarjiyantoAfiliasi tidak diketahui1
Fitrat UmirovAfiliasi tidak diketahui1
Asman ManafAfiliasi tidak diketahui1
Syafril SyahbuddinAfiliasi tidak diketahui1

Afiliasi berasal dari OpenAlex; metadata OAI-PMH jurnal tidak memuatnya. Penulis tanpa ID OpenAlex dicocokkan berdasarkan nama, sehingga dua orang bisa tergabung atau satu orang bisa terpisah.

Sumber metadata: OAI-PMH (metadata jurnal) https://univmed.org/ejurnal/index.php/medicina/oai, pertama di-harvest 10 Nov 2026, terakhir terlihat 10 Nov 2026.
Metadata asli (oai_dc)
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	<dc:title xml:lang="en">Pituitary macroadenoma with optic chiasm compression and hypopituitarism: a case report</dc:title>
	<dc:creator xml:lang="en">Kam, Alexander</dc:creator>
	<dc:creator xml:lang="en">Aprilia, Dinda</dc:creator>
	<dc:creator xml:lang="en">Decroli, Eva</dc:creator>
	<dc:subject xml:lang="en">Pituitary macroadenoma</dc:subject>
	<dc:subject xml:lang="en">optic chiasm compression</dc:subject>
	<dc:subject xml:lang="en">hyperprolactinemia</dc:subject>
	<dc:subject xml:lang="en">secondary adrenal insufficiency</dc:subject>
	<dc:subject xml:lang="en">transsphenoidal surgery</dc:subject>
	<dc:subject xml:lang="en">Pituitary macroadenoma</dc:subject>
	<dc:subject xml:lang="en">optic chiasm compression</dc:subject>
	<dc:subject xml:lang="en">hyperprolactinemia</dc:subject>
	<dc:subject xml:lang="en">secondary adrenal insufficiency</dc:subject>
	<dc:subject xml:lang="en"> transsphenoidal surgery</dc:subject>
	<dc:description xml:lang="en">INTRODUCTIONPituitary macroadenomas are benign pituitary tumors measuring more than 1 cm in diameter that constitute a substantial proportion of intracranial neoplasms. Despite their benign histology, these tumors may lead to significant morbidity due to local mass effects and endocrine dysfunction. Compression of the optic chiasm can result in progressive visual impairment and irreversible blindness if not promptly treated. Additionally, pituitary hormonal deficiencies may cause life-threatening metabolic and systemic complications. Early recognition and multidisciplinary management are therefore essential to prevent permanent sequelae and optimize functional recovery.
Case DescriptionA 40-year-old woman presented with a one-year history of recurrent headaches accompanied by progressive blurring of vision, diplopia, and visual field defects. She also reported irregular menstruation and unintended weight loss. Brain magnetic resonance imaging demonstrated a 2.13 × 2.28 × 3.05 cm pituitary macroadenoma with a characteristic “snowman appearance” compressing the optic chiasm. Hormonal evaluation revealed secondary adrenal insufficiency, hypogonadotropic hypogonadism, suppressed thyroid-stimulating hormone (TSH) with elevated free thyroxine (T4), and hyperprolactinemia attributed to the stalk effect, consistent with hypopituitarism and thyroid dysfunction. Initial stabilization with hydrocortisone and methimazole was performed prior to definitive management. The patient subsequently underwent transsphenoidal tumor resection with appropriate perioperative glucocorticoid coverage. Postoperatively, she remained clinically stable with improvement in headache and visual symptoms, and continued hormonal therapy under close endocrinological supervision.
ConclusionsThis case underscores the importance of comprehensive hormonal assessment, timely neurosurgical intervention, and coordinated multidisciplinary care in managing pituitary macroadenomas complicated by optic chiasm compression and hypopituitarism to achieve favorable clinical outcomes.</dc:description>
	<dc:publisher xml:lang="en">Faculty of Medicine, Universitas Trisakti</dc:publisher>
	<dc:date>2026-04-27</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://univmed.org/ejurnal/index.php/medicina/article/view/1763</dc:identifier>
	<dc:identifier>10.18051/UnivMed.2026.v45.81-87</dc:identifier>
	<dc:source xml:lang="en">Universa Medicina; Vol. 45 No. 1 (2026); 81-87</dc:source>
	<dc:source>2407-2230</dc:source>
	<dc:source>1907-3062</dc:source>
	<dc:source>10.18051/UnivMed.2026.v45.i1</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://univmed.org/ejurnal/index.php/medicina/article/view/1763/867</dc:relation>
	<dc:rights xml:lang="en">Copyright (c) 2026 Alexander Kam, Dinda Aprilia, Eva Decroli</dc:rights>
	<dc:rights xml:lang="en">https://creativecommons.org/licenses/by-nc-sa/4.0</dc:rights>
</oai_dc:dc>