Clival ectopic pituitary prolactinoma was successfully managed by transsphenoidal surgery: A rare case report

Author:

Mansour Marah12ORCID,Khozamah Zeinah3,Naksho Abdulmonem45,Zayat Roaa6,Al Sabbagh Aliaa6,Deeb Ahmad17

Affiliation:

1. Faculty of Medicine Tartous University Tartous Syria

2. Division of Colon and Rectal Surgery, Department of Surgery Mayo Clinic Hospital Rochester Minnesota USA

3. Department of ENT Ibn Al‐Nafees Hospital Damascus Syria

4. MSc Global Public Health Nutrition, School of Life Sciences University of Westminster London UK

5. Doctor of Medicine, Faculty of Medicine AlBaath University Homs Syria

6. Faculty of Medicine University of Damascus Damascus Syria

7. Department of ENT Al Basel Hospital Syria

Abstract

Key Clinical MessageEctopic pituitary adenoma is a rare neoplasm located in the clivus and could mimic other clival tumors. Diagnosis and treatment could be challenging. It should be considered in the differential diagnosis of clival tumors.AbstractEctopic pituitary adenomas (EPAs) are isolated adenomas that can be located in variable locations outside the sella turcica and have a normal‐appearing pituitary gland. These tumors are rare and are thought to often arise from embryological remnants along the route of Rathke's pouch migration. EPAs are associated with a wide range of clinical manifestations depending on hormonal activity and involvement of adjacent structures, which can represent a challenge in making the diagnosis and deciding on the most appropriate management. In this case study, we report a 47‐year‐old male who presented with visual disturbances, a headache, and generalized weakness. Magnetic resonance imaging showed a 2 cm mass located in the clivus invading the sphenoid sinus with an intact pituitary gland. The patient underwent endoscopic transsphenoidal surgery to eradicate the mass while maintaining the integrity of the pituitary gland, which was successful and uneventful. Pathological studies were consistent with prolactinoma, with no cytological malignant features. Post‐surgery, symptoms notably improved, and serum prolactin levels significantly dropped, The patient's condition was satisfactory on follow‐up with no long‐term complications reported. This paper contributes to the existing literature by sharing the clinical management of a challenging and uncommon case.

Publisher

Wiley

Subject

General Medicine

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