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August 20, 2025Journal of Diabetes and Endocrine Association of NepalOpen Access

A rare association of Craniopharyngioma and Meyer-Rokitansky-Kuster-Hauser Syndrome in a patient with primary amenorrhea and delayed puberty – A Case Report

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Authors

TSTaimur T. ShahPSPanna Lal SahDMD Mall

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Overview

Case report describes craniopharyngioma leading to hormonal deficiencies in a patient with MRKH syndrome, suggesting potential associations.

Key Points

  • Patient experienced primary amenorrhea, headache, and visual defects, resulting in the diagnosis of craniopharyngioma.
  • Surgical intervention included transsphenoidal resection for the craniopharyngioma and hormone replacement therapy.
  • Diagnosis revealed Type 1 MRKH syndrome alongside multiple pituitary hormone deficiencies, complicating reproductive health.
  • Future genetic testing may clarify potential etiological links between craniopharyngioma and MRKH syndrome.

Cite This Study

Shah et al. (2025) studied this question.

synapsesocial.com/papers/68af409acf1dd9ea359ec8dahttps://doi.org/10.3126/jdean.v9i2.83002
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1P44 - A strange case of primary amenorrhea2025
  2. 2The Coexistence of Gonadal Dysgenesis and the Mayer-Rokitansky-Kuster Hauser Syndrome in a girl with a 46, XX karyotype: A Rare Case Report2025
  3. 3P05 | Could diabetes correlate with a congenital disorder?2025
  4. 4Primary Amenorrhea due to Mayer–Rokitansky–Küster–Hauser (MRKH) Syndrome Managed with Laparoscopic Davydov Procedure: A Case Report2025
  5. 5Rare case of leiomyoma and endometriosis in Mayer–Rokitansky–Kuster–Hauser Syndrome2025