Giant Prolactinoma of Young Onset: A Clue to Diagnosis of MEN-1 Syndrome
Multiple endocrine neoplasia (MEN) type 1 syndrome is an autosomal dominant disorder caused by germline mutations in MEN1 gene, characterized by tumours in endocrine and nonendocrine organs. Giant prolactinoma is defined as tumours larger than 40mm with very high prolactin secretion. We report two u...
Saved in:
Main Authors: | Chandrika Jayakanthi Subasinghe, Noel Somasundaram, Pathmanathan Sivatharshya, Lalana Devi Ranasinghe, Márta Korbonits |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2018-01-01
|
Series: | Case Reports in Endocrinology |
Online Access: | http://dx.doi.org/10.1155/2018/2875074 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Giant prolactinoma with progressive cranial settling and central herniation: a case report
by: Taha Shahbazi, et al.
Published: (2024-12-01) -
Correction: Giant prolactinoma with progressive cranial settling and central herniation: a case report
by: Taha Shahbazi, et al.
Published: (2025-01-01) -
Prolactinoma: A Massive Effect on Bone Mineral Density in a Young Patient
by: Scott Sperling, et al.
Published: (2016-01-01) -
Long-Term Clinical Outcomes of Invasive Giant Prolactinomas after a Mean Ten-Year Followup
by: Ze Rui Wu, et al.
Published: (2016-01-01) -
Chromosome 22q11.2 Deletion Syndrome Presenting as Adult Onset Hypoparathyroidism: Clues to Diagnosis from Dysmorphic Facial Features
by: Sira Korpaisarn, et al.
Published: (2013-01-01)